Frequent concomitant inactivation of miR-34a and miR-34b/c by CpG methylation in colorectal, pancreatic, mammary, ovarian, urothelial, and renal cell carcinomas and soft tissue sarcomas

The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its prom...

Full description

Saved in:
Bibliographic Details
Published in:Virchows Archiv : an international journal of pathology Vol. 458; no. 3; pp. 313 - 322
Main Authors: Vogt, Markus, Munding, Johanna, Grüner, Martha, Liffers, Sven-Thorsten, Verdoodt, Berlinda, Hauk, Jennifer, Steinstraesser, Lars, Tannapfel, Andrea, Hermeking, Heiko
Format: Journal Article
Language:English
Published: Berlin/Heidelberg Springer-Verlag 01.03.2011
Springer
Springer Nature B.V
Subjects:
p53
Gut
ISSN:0945-6317, 1432-2307, 1432-2307
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a , 99% miR-34b/c ; n  = 114), pancreatic cancer (64%, 100%; n  = 11), mammary cancer (60%, 90%; n  = 10), ovarian cancer (62%, 69%; n  = 13), urothelial cancer (71%, 57%; n  = 7), and renal cell cancer (58%, 100%; n  = 12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n  = 11), in explanted, cultured cells (53%, 40%; n  = 40), and in frozen tissue samples (75%, 75%, n  = 8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.
AbstractList The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a, 99% miR-34b/c; n=114), pancreatic cancer (64%, 100%; n=11), mammary cancer (60%, 90%; n=10), ovarian cancer (62%, 69%; n=13), urothelial cancer (71%, 57%; n=7), and renal cell cancer (58%, 100%; n=12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n=11), in explanted, cultured cells (53%, 40%; n=40), and in frozen tissue samples (75%, 75%, n=8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.
The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a, 99% miR-34b/c; n=114), pancreatic cancer (64%, 100%; n=11), mammary cancer (60%, 90%; n=10), ovarian cancer (62%, 69%; n=13), urothelial cancer (71%, 57%; n=7), and renal cell cancer (58%, 100%; n=12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n=11), in explanted, cultured cells (53%, 40%; n=40), and in frozen tissue samples (75%, 75%, n=8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.[PUBLICATION ABSTRACT]
The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a, 99% miR-34b/c; n = 114), pancreatic cancer (64%, 100%; n = 11), mammary cancer (60%, 90%; n = 10), ovarian cancer (62%, 69%; n = 13), urothelial cancer (71%, 57%; n = 7), and renal cell cancer (58%, 100%; n = 12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n = 11), in explanted, cultured cells (53%, 40%; n = 40), and in frozen tissue samples (75%, 75%, n = 8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a, 99% miR-34b/c; n = 114), pancreatic cancer (64%, 100%; n = 11), mammary cancer (60%, 90%; n = 10), ovarian cancer (62%, 69%; n = 13), urothelial cancer (71%, 57%; n = 7), and renal cell cancer (58%, 100%; n = 12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n = 11), in explanted, cultured cells (53%, 40%; n = 40), and in frozen tissue samples (75%, 75%, n = 8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.
The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell cycle arrest, and senescence. We previously reported that the miR-34a gene is subject to epigenetic inactivation by CpG methylation of its promoter region in primary prostate cancer and melanomas, and in 110 different cancer cell lines of diverse origin. Here we analyzed the methylation status of miR-34a and miR-34b/c in additional primary tumors of divergent sites. We found methylation of miR-34a or miR-34b/c in formalin-fixed, paraffin-embedded (FFPE) tumor samples from 178 patients with the following frequencies: colorectal cancer (74% miR-34a , 99% miR-34b/c ; n  = 114), pancreatic cancer (64%, 100%; n  = 11), mammary cancer (60%, 90%; n  = 10), ovarian cancer (62%, 69%; n  = 13), urothelial cancer (71%, 57%; n  = 7), and renal cell cancer (58%, 100%; n  = 12). Furthermore, soft tissue sarcomas showed methylation of miR-34 gene promoters in FFPE samples (64%, 45%; n  = 11), in explanted, cultured cells (53%, 40%; n  = 40), and in frozen tissue samples (75%, 75%, n  = 8). In the colorectal cancer samples a statistically significant correlation of miR-34a methylation and the absence of p53 mutation was detected. With the exception of sarcoma cell lines, the inactivation of miR-34a and miR-34b/c was concomitant in most cases. These results show that miR-34 inactivation is a common event in tumor formation, and suggest that CpG methylation of miR-34a and miR-34-b/c may have diagnostic value. The mutual exclusiveness of miR-34a methylation and p53 mutation indicates that miR-34a inactivation may substitute for loss of p53 function in cancer.
Author Grüner, Martha
Liffers, Sven-Thorsten
Hauk, Jennifer
Tannapfel, Andrea
Vogt, Markus
Verdoodt, Berlinda
Munding, Johanna
Hermeking, Heiko
Steinstraesser, Lars
Author_xml – sequence: 1
  givenname: Markus
  surname: Vogt
  fullname: Vogt, Markus
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 2
  givenname: Johanna
  surname: Munding
  fullname: Munding, Johanna
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 3
  givenname: Martha
  surname: Grüner
  fullname: Grüner, Martha
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 4
  givenname: Sven-Thorsten
  surname: Liffers
  fullname: Liffers, Sven-Thorsten
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 5
  givenname: Berlinda
  surname: Verdoodt
  fullname: Verdoodt, Berlinda
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 6
  givenname: Jennifer
  surname: Hauk
  fullname: Hauk, Jennifer
  organization: Department of Plastic and Reconstructive Surgery, Department of Hand Surgery, Soft Tissue Tumour Reference Centre, BG University Hospital Bergmannsheil, Ruhr University Bochum
– sequence: 7
  givenname: Lars
  surname: Steinstraesser
  fullname: Steinstraesser, Lars
  organization: Department of Plastic and Reconstructive Surgery, Department of Hand Surgery, Soft Tissue Tumour Reference Centre, BG University Hospital Bergmannsheil, Ruhr University Bochum
– sequence: 8
  givenname: Andrea
  surname: Tannapfel
  fullname: Tannapfel, Andrea
  organization: Institute of Pathology, Ruhr-University-Bochum
– sequence: 9
  givenname: Heiko
  surname: Hermeking
  fullname: Hermeking, Heiko
  email: heiko.hermeking@med.uni-muenchen.de
  organization: Institute of Pathology, Ruhr-University-Bochum, Experimental and Molecular Pathology, Institute of Pathology, Ludwig-Maximilians-University Munich
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23947296$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/21225432$$D View this record in MEDLINE/PubMed
BookMark eNp9kt1qFDEUx4NU7Lb6AN5IEEQvdmw-JpnJZVlsFQqC6PVw9mzGpswka5Ip7KP5dmZ2VwsFe5Oc8P-dk_N1Rk588JaQ15x95Iw1F4mxWrQV46ziTLJKPSMLXktRCcmaE7JgplaVlrw5JWcp3TEmeMv1C3IquBCqgAvy-yraX5P1mWLwGEaXodjOA2Z3D9kFT0NPR_etkjVQ8Jujvb5Aut7R1faajjbf7oYD63yJM4RoMcOwpFvwGG2RcElHGEeIuyUN9xAd-CWdYsi3dnAzOUeO1sNA0Q7lgIjOhxHSXkmhzzS7lCZLU5Fm4SV53sOQ7KvjfU5-XH36vvpc3Xy9_rK6vKmwNiZX2K9BoKmtUYjYa4VirRUYrQVrWuw3DYBppDKMt6ChiJuNFo3BVgnRYC3PyftD3G0MpVMpd6NLc5LgbZhS1yppjJR8Jj88SfJat1IJplRB3z5C78IUS_n7eIoprk2B3hyhaT3aTbeNbu5g93d6BXh3BCAhDH0s7XbpgZOmboTRheMHDmNIKdr-H8JZN29Sd9ikju3fknVzhs0jHyy7MQ85R3DDk57i4JnKL_6njQ-1_d_pDxz03Jc
CitedBy_id crossref_primary_10_1016_j_jbior_2019_04_004
crossref_primary_10_1053_j_gastro_2015_07_011
crossref_primary_10_1038_bjc_2016_454
crossref_primary_10_1016_j_bcp_2011_12_026
crossref_primary_10_1016_j_molonc_2012_07_007
crossref_primary_10_1016_j_bbagen_2012_10_014
crossref_primary_10_1016_j_omton_2024_200765
crossref_primary_10_1093_carcin_bgr286
crossref_primary_10_2217_epi_12_39
crossref_primary_10_1261_rna_052571_115
crossref_primary_10_1007_s12035_014_8803_9
crossref_primary_10_1158_1541_7786_MCR_12_0274
crossref_primary_10_3892_ol_2018_9575
crossref_primary_10_1038_s41418_023_01193_2
crossref_primary_10_1016_j_jpedsurg_2016_02_091
crossref_primary_10_1186_1476_4598_13_115
crossref_primary_10_1016_j_cll_2018_02_003
crossref_primary_10_3892_or_2014_3142
crossref_primary_10_1134_S1022795413030034
crossref_primary_10_1074_jbc_AC119_010419
crossref_primary_10_1097_MD_0000000000025827
crossref_primary_10_1002_ijc_27345
crossref_primary_10_1007_s11888_011_0116_z
crossref_primary_10_1016_j_gene_2016_12_018
crossref_primary_10_1002_jcp_27990
crossref_primary_10_3892_ijmm_2018_4003
crossref_primary_10_1038_s41418_023_01178_1
crossref_primary_10_1371_journal_pgen_1002363
crossref_primary_10_1158_1078_0432_CCR_12_2952
crossref_primary_10_1186_s13046_019_1059_5
crossref_primary_10_1002_jcp_28160
crossref_primary_10_3233_CBM_170289
crossref_primary_10_1038_s41598_020_66561_1
crossref_primary_10_3892_ijo_2024_5650
crossref_primary_10_1016_j_semcancer_2020_05_017
crossref_primary_10_1016_j_cll_2013_08_001
crossref_primary_10_1016_j_molonc_2016_03_008
crossref_primary_10_1134_S1022795418070086
crossref_primary_10_1038_bjc_2013_449
crossref_primary_10_1002_ijc_29413
crossref_primary_10_1158_0008_5472_CAN_16_2183
crossref_primary_10_1016_j_addr_2014_10_020
crossref_primary_10_1002_gcc_22332
crossref_primary_10_4161_epi_25927
crossref_primary_10_1007_s00204_016_1815_7
crossref_primary_10_4161_cc_25135
crossref_primary_10_1158_1078_0432_CCR_13_0736
crossref_primary_10_1038_s41417_020_00210_7
crossref_primary_10_2217_epi_11_93
crossref_primary_10_3748_wjg_v20_i32_11199
crossref_primary_10_1038_cgt_2016_77
crossref_primary_10_1038_bjc_2012_537
crossref_primary_10_1289_ehp_1408459
crossref_primary_10_3390_ijms19092791
crossref_primary_10_1038_s41419_018_0777_5
crossref_primary_10_3892_ol_2020_11837
crossref_primary_10_1016_j_yexmp_2015_06_014
crossref_primary_10_1007_s11033_012_2063_4
crossref_primary_10_1007_s00438_014_0960_z
crossref_primary_10_1016_j_acthis_2020_151576
crossref_primary_10_1016_j_canlet_2014_05_022
crossref_primary_10_1186_s13045_016_0323_9
crossref_primary_10_1038_ki_2011_448
crossref_primary_10_1016_j_jgg_2013_03_002
crossref_primary_10_1016_j_jgg_2018_03_001
crossref_primary_10_1016_j_phrs_2013_03_006
crossref_primary_10_3389_fgene_2024_1461404
crossref_primary_10_1002_jcp_26095
crossref_primary_10_1016_j_ajpath_2014_10_006
crossref_primary_10_3390_cancers13061333
crossref_primary_10_1111_bju_12551
crossref_primary_10_1007_s13277_014_2861_5
crossref_primary_10_1186_1756_9966_33_20
crossref_primary_10_1007_s40291_019_00381_6
crossref_primary_10_1073_pnas_1703029115
crossref_primary_10_1016_j_gene_2014_03_059
crossref_primary_10_1016_j_ajpath_2017_06_014
crossref_primary_10_1038_nrc3265
crossref_primary_10_1007_s11033_015_3860_3
crossref_primary_10_3390_pharmaceutics17081084
crossref_primary_10_1080_14737159_2017_1337511
crossref_primary_10_1158_1940_6207_CAPR_14_0357
crossref_primary_10_1007_s00018_021_03979_4
crossref_primary_10_1158_1078_0432_CCR_12_1703
crossref_primary_10_3892_ol_2013_1428
crossref_primary_10_1007_s00432_014_1690_7
crossref_primary_10_1016_j_yexmp_2014_08_002
crossref_primary_10_1007_s40495_015_0016_z
crossref_primary_10_1038_s41417_020_00224_1
crossref_primary_10_1186_s12885_016_2253_x
crossref_primary_10_2217_fon_13_259
crossref_primary_10_1134_S1022795415050026
crossref_primary_10_1016_j_jacc_2012_02_033
crossref_primary_10_1038_s41467_021_21162_y
crossref_primary_10_1007_s13277_014_2572_y
crossref_primary_10_1007_s40495_014_0008_4
crossref_primary_10_1053_j_gastro_2012_09_032
crossref_primary_10_1158_0008_5472_CAN_15_2321
crossref_primary_10_1586_erm_13_38
crossref_primary_10_1038_nrc3447
crossref_primary_10_1016_j_ymeth_2012_09_002
crossref_primary_10_1158_0008_5472_CAN_12_0803
crossref_primary_10_3892_ol_2019_10092
crossref_primary_10_1016_j_clinre_2014_10_007
crossref_primary_10_3389_fgene_2019_00320
crossref_primary_10_1111_jcmm_12368
crossref_primary_10_1038_cddis_2017_495
crossref_primary_10_1016_j_cllc_2016_06_005
crossref_primary_10_1016_j_euf_2015_11_006
crossref_primary_10_1038_ncb3611
crossref_primary_10_1155_2014_678401
crossref_primary_10_1371_journal_pone_0117107
crossref_primary_10_3390_ijms19020459
crossref_primary_10_1155_2013_719202
crossref_primary_10_3389_fbioe_2022_911769
crossref_primary_10_1016_j_neulet_2017_04_061
crossref_primary_10_3892_mmr_2018_9182
crossref_primary_10_1007_s10552_013_0187_z
crossref_primary_10_1371_journal_pone_0124899
crossref_primary_10_1007_s10534_015_9872_6
crossref_primary_10_1016_j_critrevonc_2018_09_006
crossref_primary_10_1016_j_stem_2013_04_018
crossref_primary_10_1016_j_ijbiomac_2017_10_154
crossref_primary_10_1158_1541_7786_MCR_14_0424
crossref_primary_10_1016_j_gene_2023_148069
crossref_primary_10_2147_OTT_S234549
crossref_primary_10_1016_j_phrs_2021_105611
crossref_primary_10_1134_S0026893318020140
crossref_primary_10_3389_fonc_2022_960269
crossref_primary_10_1002_lary_25475
crossref_primary_10_1007_s00595_012_0392_5
crossref_primary_10_1097_MD_0000000000005050
crossref_primary_10_1097_MD_0000000000023716
crossref_primary_10_1016_j_snb_2021_129624
crossref_primary_10_3892_etm_2012_585
crossref_primary_10_1007_s00441_014_1793_0
crossref_primary_10_1074_jbc_M111_280768
crossref_primary_10_1186_s12951_024_02559_5
crossref_primary_10_1038_srep09742
crossref_primary_10_1586_erm_12_39
crossref_primary_10_1007_s00296_015_3260_y
crossref_primary_10_1007_s12032_014_0894_7
crossref_primary_10_1530_REP_14_0239
crossref_primary_10_3390_cancers5020676
crossref_primary_10_1016_j_yexmp_2017_05_012
crossref_primary_10_3390_ijms20184600
crossref_primary_10_1016_j_bbcan_2012_01_004
crossref_primary_10_1038_clpt_2012_192
crossref_primary_10_1016_j_bbcan_2016_01_001
crossref_primary_10_1007_s12253_020_00842_y
crossref_primary_10_1093_humupd_dmr041
crossref_primary_10_1155_2022_7214904
crossref_primary_10_1007_s00210_024_03594_7
crossref_primary_10_2217_epi_15_6
crossref_primary_10_1093_mutage_geu001
crossref_primary_10_1007_s00018_015_2020_1
crossref_primary_10_1002_path_4037
crossref_primary_10_1007_s11033_013_2998_0
crossref_primary_10_1053_j_gastro_2018_08_011
crossref_primary_10_3390_ijms25084157
crossref_primary_10_1134_S0006297915020029
crossref_primary_10_1016_j_ajpath_2018_10_005
crossref_primary_10_3748_wjg_v20_i45_17011
crossref_primary_10_1002_jcp_26116
crossref_primary_10_1158_0008_5472_CAN_12_2230
crossref_primary_10_1016_j_biopha_2013_10_002
crossref_primary_10_3892_ol_2016_5033
crossref_primary_10_1038_s41420_022_01054_w
crossref_primary_10_1002_mc_22296
crossref_primary_10_1016_j_clinbiochem_2013_03_019
crossref_primary_10_1371_journal_pone_0135991
crossref_primary_10_3390_cancers16091681
crossref_primary_10_1016_j_ejca_2016_12_018
crossref_primary_10_1371_journal_pone_0080570
crossref_primary_10_1038_s41388_018_0390_1
crossref_primary_10_1155_2015_892903
crossref_primary_10_1016_j_canep_2014_06_005
crossref_primary_10_1080_00365521_2017_1301989
crossref_primary_10_1016_j_bbagrm_2014_04_003
crossref_primary_10_1038_s41585_018_0023_z
crossref_primary_10_1038_onc_2012_311
crossref_primary_10_7717_peerj_15777
crossref_primary_10_3390_ph6101195
crossref_primary_10_1186_s12885_017_3638_1
crossref_primary_10_1016_j_arcmed_2019_05_008
crossref_primary_10_3390_ijms232012381
crossref_primary_10_1016_j_yexmp_2015_03_017
crossref_primary_10_1016_j_cancergen_2012_03_001
crossref_primary_10_1016_j_toxlet_2019_11_012
crossref_primary_10_3390_cancers13164072
crossref_primary_10_1186_1756_8722_5_58
crossref_primary_10_3390_antiox12050997
crossref_primary_10_1093_bib_bbac390
crossref_primary_10_1517_14728222_2016_1114102
crossref_primary_10_4161_epi_19464
crossref_primary_10_1007_s12032_012_0413_7
crossref_primary_10_3892_ol_2021_13066
crossref_primary_10_1016_j_jpedsurg_2016_09_070
crossref_primary_10_1016_j_neurobiolaging_2013_10_082
crossref_primary_10_1186_s12885_016_2135_2
crossref_primary_10_1016_j_fertnstert_2013_09_009
crossref_primary_10_1016_j_genrep_2021_101416
crossref_primary_10_1038_nrurol_2012_104
crossref_primary_10_3390_biomedicines3010032
Cites_doi 10.1126/science.1140735
10.1002/ijc.25269
10.1146/annurev.med.59.053006.104707
10.1093/carcin/bgq033
10.1038/nature05939
10.1073/pnas.0910015107
10.1038/cdd.2009.109
10.1200/JCO.2005.00.471
10.1073/pnas.0803055105
10.1016/j.cell.2007.01.029
10.1158/0008-5472.CAN-08-2148
10.1016/j.molcel.2007.05.010
10.1158/0008-5472.CAN-10-0655
10.4161/cc.6.13.4436
10.1002/humu.10175
10.1158/0008-5472.CAN-09-0529
10.1200/JCO.2005.07.021
10.1158/1078-0432.CCR-09-2642
10.1016/j.canlet.2008.09.035
10.1158/0008-5472.CAN-08-0325
10.1371/journal.pone.0006816
10.4161/cc.7.16.6533
10.1016/j.molcel.2007.05.017
10.1038/nrg2634
10.1158/0008-5472.CAN-07-1585
10.1038/cdd.2009.56
10.1073/pnas.0707351104
10.1016/j.cub.2007.06.068
10.1038/sj.onc.1210293
10.1073/pnas.93.18.9821
10.1093/carcin/bgp219
10.1038/nrc1045
10.1016/j.ccr.2007.10.028
10.1038/nrg816
ContentType Journal Article
Copyright Springer-Verlag 2011
2015 INIST-CNRS
Copyright_xml – notice: Springer-Verlag 2011
– notice: 2015 INIST-CNRS
DBID AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7RV
7T5
7T7
7TM
7TO
7U7
7U9
7X7
7XB
88A
88E
8AO
8FD
8FE
8FH
8FI
8FJ
8FK
ABUWG
AEUYN
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
C1K
CCPQU
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
H94
HCIFZ
K9.
KB0
LK8
M0S
M1P
M7P
NAPCQ
P64
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
DOI 10.1007/s00428-010-1030-5
DatabaseName CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Nursing & Allied Health Database
Immunology Abstracts
Industrial and Applied Microbiology Abstracts (Microbiology A)
Nucleic Acids Abstracts
Oncogenes and Growth Factors Abstracts
Toxicology Abstracts
Virology and AIDS Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
Technology Research Database
ProQuest SciTech Collection
ProQuest Natural Science Collection
ProQuest Hospital Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest One Sustainability
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
Environmental Sciences and Pollution Management
ProQuest One Community College
ProQuest Central
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
AIDS and Cancer Research Abstracts
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
Biological Sciences
ProQuest Health & Medical Collection
PML(ProQuest Medical Library)
Biological Science Database
Nursing & Allied Health Premium
Biotechnology and BioEngineering Abstracts
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic (retired)
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest Central Student
Oncogenes and Growth Factors Abstracts
ProQuest Central Essentials
Nucleic Acids Abstracts
SciTech Premium Collection
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
Health Research Premium Collection
Natural Science Collection
Health & Medical Research Collection
Biological Science Collection
Industrial and Applied Microbiology Abstracts (Microbiology A)
ProQuest Central (New)
ProQuest Medical Library (Alumni)
Virology and AIDS Abstracts
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest Nursing & Allied Health Source (Alumni)
Engineering Research Database
ProQuest One Academic
ProQuest One Academic (New)
Technology Research Database
ProQuest One Academic Middle East (New)
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
ProQuest Health & Medical Research Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
AIDS and Cancer Research Abstracts
Toxicology Abstracts
ProQuest Nursing & Allied Health Source
ProQuest SciTech Collection
ProQuest Medical Library
Immunology Abstracts
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList Nucleic Acids Abstracts
ProQuest Central Student
MEDLINE - Academic

MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1432-2307
EndPage 322
ExternalDocumentID 2274987111
21225432
23947296
10_1007_s00428_010_1030_5
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
-53
-5E
-5G
-BR
-EM
-Y2
-~C
.55
.86
.GJ
.VR
04C
06C
06D
0R~
0VY
1N0
2.D
203
28-
29Q
29~
2J2
2JN
2JY
2KG
2KM
2LR
2P1
2VQ
2~H
30V
3O-
3V.
4.4
406
408
409
40D
40E
53G
5QI
5RE
5VS
67Z
6NX
78A
7RV
7X7
88A
88E
8AO
8FE
8FH
8FI
8FJ
8TC
8UJ
95-
95.
95~
96X
AAAVM
AABHQ
AACDK
AAHNG
AAIAL
AAJBT
AAJKR
AANXM
AANZL
AARHV
AARTL
AASML
AATNV
AATVU
AAUYE
AAWCG
AAWTL
AAYIU
AAYQN
AAYTO
AAYZH
ABAKF
ABBBX
ABBXA
ABDZT
ABECU
ABFTV
ABHLI
ABHQN
ABIPD
ABJNI
ABJOX
ABKCH
ABKTR
ABLJU
ABMNI
ABMQK
ABNWP
ABOCM
ABPLI
ABQBU
ABQSL
ABSXP
ABTEG
ABTKH
ABTMW
ABULA
ABUWG
ABWNU
ABXPI
ACAOD
ACBXY
ACDTI
ACGFS
ACHSB
ACHXU
ACKNC
ACMDZ
ACMLO
ACOKC
ACOMO
ACPIV
ACPRK
ACUDM
ACZOJ
ADBBV
ADHIR
ADIMF
ADINQ
ADJJI
ADKNI
ADKPE
ADRFC
ADTPH
ADURQ
ADYFF
ADZKW
AEBTG
AEFIE
AEFQL
AEGAL
AEGNC
AEJHL
AEJRE
AEKMD
AEMSY
AENEX
AEOHA
AEPYU
AESKC
AETLH
AEUYN
AEVLU
AEXYK
AFBBN
AFEXP
AFFNX
AFKRA
AFLOW
AFQWF
AFRAH
AFWTZ
AFZKB
AGAYW
AGDGC
AGGDS
AGJBK
AGMZJ
AGQEE
AGQMX
AGWIL
AGWZB
AGYKE
AHAVH
AHBYD
AHIZS
AHMBA
AHSBF
AHYZX
AIAKS
AIGIU
AIIXL
AILAN
AITGF
AJBLW
AJRNO
AJZVZ
AKMHD
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALWAN
AMKLP
AMXSW
AMYLF
AOCGG
ARMRJ
ASPBG
AVWKF
AXYYD
AZFZN
B-.
BA0
BBNVY
BBWZM
BDATZ
BENPR
BGNMA
BHPHI
BKEYQ
BMSDO
BPHCQ
BSONS
BVXVI
CAG
CCPQU
COF
CSCUP
DDRTE
DL5
DNIVK
DPUIP
DU5
EBLON
EBS
EIHBH
EIOEI
EJD
EMOBN
EN4
ESBYG
EX3
F5P
FEDTE
FERAY
FFXSO
FIGPU
FINBP
FNLPD
FRRFC
FSGXE
FWDCC
FYUFA
G-Y
G-Z
GGCAI
GGRSB
GJIRD
GNWQR
GQ6
GQ7
GQ8
GRRUI
GXS
H13
HCIFZ
HF~
HG5
HG6
HMCUK
HMJXF
HQYDN
HRMNR
HVGLF
HZ~
I09
IHE
IJ-
IKXTQ
IMOTQ
ITM
IWAJR
IXC
IZIGR
IZQ
I~X
I~Z
J-C
J0Z
JBSCW
JCJTX
JZLTJ
KDC
KOV
KOW
KPH
LAS
LK8
LLZTM
M0L
M1P
M4Y
M7P
MA-
N2Q
N9A
NAPCQ
NB0
NDZJH
NPVJJ
NQJWS
NU0
O9-
O93
O9G
O9I
O9J
OAM
P19
P2P
P9S
PF0
PQQKQ
PROAC
PSQYO
PT4
PT5
Q2X
QOK
QOR
QOS
R89
R9I
RHV
RIG
RNI
RNS
RPX
RRX
RSV
RZK
S16
S1Z
S26
S27
S28
S37
S3B
SCLPG
SDE
SDH
SDM
SHX
SISQX
SJYHP
SMD
SNE
SNPRN
SNX
SOHCF
SOJ
SPISZ
SRMVM
SSLCW
SSXJD
STPWE
SV3
SZ9
SZN
T13
T16
TSG
TSK
TSV
TT1
TUC
U2A
U9L
UG4
UKHRP
UOJIU
UTJUX
UZXMN
VC2
VFIZW
W23
W48
WJK
WK8
WOW
X7M
YLTOR
Z45
Z7U
Z81
Z82
Z87
Z8O
Z8U
Z8V
Z91
ZGI
ZMTXR
ZOVNA
~EX
AAPKM
AAYXX
ABBRH
ABDBE
ABFSG
ABRTQ
ACSTC
ADHKG
AEZWR
AFDZB
AFFHD
AFHIU
AFOHR
AGQPQ
AHPBZ
AHWEU
AIXLP
ATHPR
AYFIA
CITATION
PHGZM
PHGZT
PJZUB
PPXIY
PQGLB
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7T5
7T7
7TM
7TO
7U7
7U9
7XB
8FD
8FK
AZQEC
C1K
DWQXO
FR3
GNUQQ
H94
K9.
P64
PKEHL
PQEST
PQUKI
PRINS
7X8
PUEGO
ID FETCH-LOGICAL-c499t-cfba2c94e95cccf65c2b65a9662078cfd7aa97359018a6a2b6dd6279c85227c43
IEDL.DBID 7RV
ISICitedReferencesCount 269
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000288679000007&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 0945-6317
1432-2307
IngestDate Fri Sep 05 11:35:17 EDT 2025
Fri Sep 05 13:24:25 EDT 2025
Tue Nov 04 21:46:43 EST 2025
Wed Feb 19 01:48:25 EST 2025
Mon Jul 21 09:12:10 EDT 2025
Tue Nov 18 22:23:43 EST 2025
Sat Nov 29 04:13:39 EST 2025
Fri Feb 21 02:35:32 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords CpG methylation
family
p53
Cancer
Epigenetic inactivation
Ovary carcinoma
miR-34a
Ovary cancer
Transitional cell carcinoma
Inactivation
TP53 Gene
GC rich sequence
Family environment
Grawitz tumor
Colon
Mammary gland
Pancreas
Tumor suppressor gene
Kidney disease
Urinary system disease
miR-34 family
Nucleotide sequence
Digestive system
Family study
Gut
Soft tissue sarcoma
Malignant tumor
Female genital diseases
Ovarian diseases
miR-34b/c
Kidney cancer
Rectum
Breast
Frequency
Methylation
Language English
License http://www.springer.com/tdm
CC BY 4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c499t-cfba2c94e95cccf65c2b65a9662078cfd7aa97359018a6a2b6dd6279c85227c43
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
PMID 21225432
PQID 853505169
PQPubID 54092
PageCount 10
ParticipantIDs proquest_miscellaneous_853993314
proquest_miscellaneous_1468352055
proquest_journals_853505169
pubmed_primary_21225432
pascalfrancis_primary_23947296
crossref_primary_10_1007_s00428_010_1030_5
crossref_citationtrail_10_1007_s00428_010_1030_5
springer_journals_10_1007_s00428_010_1030_5
PublicationCentury 2000
PublicationDate 2011-03-01
PublicationDateYYYYMMDD 2011-03-01
PublicationDate_xml – month: 03
  year: 2011
  text: 2011-03-01
  day: 01
PublicationDecade 2010
PublicationPlace Berlin/Heidelberg
PublicationPlace_xml – name: Berlin/Heidelberg
– name: Heidelberg
– name: Germany
PublicationSubtitle The European Journal of Pathology
PublicationTitle Virchows Archiv : an international journal of pathology
PublicationTitleAbbrev Virchows Arch
PublicationTitleAlternate Virchows Arch
PublicationYear 2011
Publisher Springer-Verlag
Springer
Springer Nature B.V
Publisher_xml – name: Springer-Verlag
– name: Springer
– name: Springer Nature B.V
References Russo, Bazan, Iacopetta, Kerr, Soussi, Gebbia (CR31) 2005; 23
Hagman, Larne, Edsjo, Bjartell, Ehrnstrom, Ulmert, Lilja, Ceder (CR24) 2010; 127
Gallardo, Navarro, Vinolas, Marrades, Diaz, Gel, Quera, Bandres, Garcia-Foncillas, Ramirez, Monzo (CR25) 2009; 30
Hermeking (CR10) 2010; 17
Jones, Baylin (CR14) 2007; 128
Raver-Shapira, Marciano, Meiri, Spector, Rosenfeld, Moskovits, Bentwich, Oren (CR6) 2007; 26
Cannell, Kong, Johnston, Chen, Collins, Dobbyn, Elia, Kress, Dickens, Clemens, Heery, Gaestel, Eilers, Willis, Bushell (CR29) 2010; 107
Corney, Hwang, Matoso, Vogt, Flesken-Nikitin, Godwin, Kamat, Sood, Ellenson, Hermeking, Nikitin (CR21) 2010; 16
Hermeking (CR2) 2007; 12
Tazawa, Tsuchiya, Izumiya, Nakagama (CR28) 2007; 104
Croce (CR3) 2009; 10
Li, Guessous, Zhang, Dipierro, Kefas, Johnson, Marcinkiewicz, Jiang, Yang, Schmittgen, Lopes, Schiff, Purow, Abounader (CR26) 2009; 69
Migliore, Petrelli, Ghiso, Corso, Capparuccia, Eramo, Comoglio, Giordano (CR23) 2008; 68
Wittekind, Bootz, Meyer (CR20) 2002
He, He, Lim, de Stanchina, Xuan, Liang, Xue, Zender, Magnus, Ridzon, Jackson, Linsley, Chen, Lowe, Cleary, Hannon (CR7) 2007; 447
Iacopetta (CR30) 2003; 21
Tarasov, Jung, Verdoodt, Lodygin, Epanchintsev, Menssen, Meister, Hermeking (CR4) 2007; 6
Laird (CR15) 2003; 3
Toyota, Suzuki, Sasaki, Maruyama, Imai, Shinomura, Tokino (CR12) 2008; 68
Christoffersen, Shalgi, Frankel, Leucci, Lees, Klausen, Pilpel, Nielsen, Oren, Lund (CR27) 2010; 17
Corney, Flesken-Nikitin, Godwin, Wang, Nikitin (CR9) 2007; 67
Welch, Chen, Stallings (CR11) 2007; 26
Halazonetis, Gorgoulis, Bartek (CR17) 2008; 319
Chim, Wong, Qi, Loong, Lam, Wong, Jin, Costello, Liang (CR34) 2010; 31
Herman, Graff, Myohanen, Nelkin, Baylin (CR19) 1996; 93
Garzon, Calin, Croce (CR1) 2009; 60
Chang, Wentzel, Kent, Ramachandran, Mullendore, Lee, Feldmann, Yamakuchi, Ferlito, Lowenstein, Arking, Beer, Maitra, Mendell (CR5) 2007; 26
Hoff (CR32) 2005; 23
Wiggins, Ruffino, Kelnar, Omotola, Patrawala, Brown, Bader (CR35) 2010; 70
Bommer, Gerin, Feng, Kaczorowski, Kuick, Love, Zhai, Giordano, Qin, Moore, Macdougald, Cho, Fearon (CR8) 2007; 17
Jones, Baylin (CR13) 2002; 3
Lujambio, Calin, Villanueva, Ropero, Sanchez-Cespedes, Blanco, Montuenga, Rossi, Nicoloso, Faller, Gallagher, Eccles, Croce, Esteller (CR18) 2008; 105
Lodygin, Tarasov, Epanchintsev, Berking, Knyazeva, Korner, Knyazev, Diebold, Hermeking (CR16) 2008; 7
Li, Fu, Tie, Hu, Kong, Wu, Zheng (CR22) 2009; 275
Ji, Hao, Zhang, Tang, Yang, Li, Xiang, Desano, Bommer, Fan, Fearon, Lawrence, Xu (CR33) 2009; 4
V Tarasov (1030_CR4) 2007; 6
M Toyota (1030_CR12) 2008; 68
Q Ji (1030_CR33) 2009; 4
Z Hagman (1030_CR24) 2010; 127
H Hermeking (1030_CR10) 2010; 17
N Raver-Shapira (1030_CR6) 2007; 26
H Tazawa (1030_CR28) 2007; 104
TD Halazonetis (1030_CR17) 2008; 319
PA Jones (1030_CR14) 2007; 128
A Russo (1030_CR31) 2005; 23
DC Corney (1030_CR21) 2010; 16
R Garzon (1030_CR1) 2009; 60
H Hermeking (1030_CR2) 2007; 12
GT Bommer (1030_CR8) 2007; 17
C Migliore (1030_CR23) 2008; 68
TC Chang (1030_CR5) 2007; 26
A Lujambio (1030_CR18) 2008; 105
D Lodygin (1030_CR16) 2008; 7
E Gallardo (1030_CR25) 2009; 30
NR Christoffersen (1030_CR27) 2010; 17
CM Wittekind (1030_CR20) 2002
CS Chim (1030_CR34) 2010; 31
B Iacopetta (1030_CR30) 2003; 21
Y Li (1030_CR26) 2009; 69
IG Cannell (1030_CR29) 2010; 107
PW Laird (1030_CR15) 2003; 3
JG Herman (1030_CR19) 1996; 93
L He (1030_CR7) 2007; 447
N Li (1030_CR22) 2009; 275
JF Wiggins (1030_CR35) 2010; 70
DC Corney (1030_CR9) 2007; 67
PA Jones (1030_CR13) 2002; 3
C Welch (1030_CR11) 2007; 26
PM Hoff (1030_CR32) 2005; 23
CM Croce (1030_CR3) 2009; 10
17554199 - Cell Cycle. 2007 Jul 1;6(13):1586-93
12042769 - Nat Rev Genet. 2002 Jun;3(6):415-28
18323444 - Science. 2008 Mar 7;319(5868):1352-5
20212154 - Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5375-80
16172461 - J Clin Oncol. 2005 Oct 20;23(30):7518-28
17554337 - Nature. 2007 Jun 28;447(7148):1130-4
18768788 - Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13556-61
18519671 - Cancer Res. 2008 Jun 1;68(11):4123-32
17875987 - Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15472-7
17540599 - Mol Cell. 2007 Jun 8;26(5):745-52
17823410 - Cancer Res. 2007 Sep 15;67(18):8433-8
19763153 - Nat Rev Genet. 2009 Oct;10(10):704-14
12619112 - Hum Mutat. 2003 Mar;21(3):271-6
17996645 - Cancer Cell. 2007 Nov;12(5):414-8
19736307 - Carcinogenesis. 2009 Nov;30(11):1903-9
17540598 - Mol Cell. 2007 Jun 8;26(5):731-43
19696787 - Cell Death Differ. 2010 Feb;17(2):236-45
20570894 - Cancer Res. 2010 Jul 15;70(14):5923-30
19006648 - Cancer Lett. 2009 Mar 8;275(1):44-53
21351256 - Int J Cancer. 2010 Dec 15;127(12):2768-76
17297439 - Oncogene. 2007 Jul 26;26(34):5017-22
19630570 - Annu Rev Med. 2009;60:167-79
19773441 - Cancer Res. 2009 Oct 1;69(19):7569-76
12671664 - Nat Rev Cancer. 2003 Apr;3(4):253-66
17656095 - Curr Biol. 2007 Aug 7;17(15):1298-307
19714243 - PLoS One. 2009 Aug 28;4(8):e6816
20145172 - Clin Cancer Res. 2010 Feb 15;16(4):1119-28
19461653 - Cell Death Differ. 2010 Feb;17(2):193-9
18719384 - Cell Cycle. 2008 Aug 15;7(16):2591-600
8790415 - Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9821-6
16186590 - J Clin Oncol. 2005 Oct 20;23(30):7395-6
20118199 - Carcinogenesis. 2010 Apr;31(4):745-50
19074879 - Cancer Res. 2008 Dec 15;68(24):10128-36
17320506 - Cell. 2007 Feb 23;128(4):683-92
References_xml – volume: 319
  start-page: 1352
  issue: 5868
  year: 2008
  end-page: 1355
  ident: CR17
  article-title: An oncogene-induced DNA damage model for cancer development
  publication-title: Science
  doi: 10.1126/science.1140735
– volume: 127
  start-page: 2768
  issue: 12
  year: 2010
  end-page: 2776
  ident: CR24
  article-title: miR-34c is down regulated in prostate cancer and exerts tumor suppressive functions
  publication-title: Int J Cancer
  doi: 10.1002/ijc.25269
– volume: 60
  start-page: 167
  year: 2009
  end-page: 179
  ident: CR1
  article-title: MicroRNAs in Cancer
  publication-title: Annu Rev Med
  doi: 10.1146/annurev.med.59.053006.104707
– volume: 3
  start-page: 415
  issue: 6
  year: 2002
  end-page: 428
  ident: CR13
  article-title: The fundamental role of epigenetic events in cancer
  publication-title: Nat Rev Genet
– volume: 31
  start-page: 745
  issue: 4
  year: 2010
  end-page: 750
  ident: CR34
  article-title: Epigenetic inactivation of the miR-34a in hematological malignancies
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgq033
– volume: 447
  start-page: 1130
  issue: 7148
  year: 2007
  end-page: 1134
  ident: CR7
  article-title: A microRNA component of the p53 tumour suppressor network
  publication-title: Nature
  doi: 10.1038/nature05939
– volume: 107
  start-page: 5375
  issue: 12
  year: 2010
  end-page: 5380
  ident: CR29
  article-title: p38 MAPK/MK2-mediated induction of miR-34c following DNA damage prevents Myc-dependent DNA replication
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0910015107
– volume: 17
  start-page: 236
  issue: 2
  year: 2010
  end-page: 245
  ident: CR27
  article-title: p53-independent upregulation of miR-34a during oncogene-induced senescence represses MYC
  publication-title: Cell Death Differ
  doi: 10.1038/cdd.2009.109
– volume: 23
  start-page: 7518
  issue: 30
  year: 2005
  end-page: 7528
  ident: CR31
  article-title: The TP53 colorectal cancer international collaborative study on the prognostic and predictive significance of p53 mutation: influence of tumor site, type of mutation, and adjuvant treatment
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2005.00.471
– volume: 105
  start-page: 13556
  issue: 36
  year: 2008
  end-page: 13561
  ident: CR18
  article-title: A microRNA DNA methylation signature for human cancer metastasis
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0803055105
– volume: 128
  start-page: 683
  issue: 4
  year: 2007
  end-page: 692
  ident: CR14
  article-title: The epigenomics of cancer
  publication-title: Cell
  doi: 10.1016/j.cell.2007.01.029
– volume: 68
  start-page: 10128
  issue: 24
  year: 2008
  end-page: 10136
  ident: CR23
  article-title: MicroRNAs impair MET-mediated invasive growth
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-08-2148
– volume: 26
  start-page: 745
  issue: 5
  year: 2007
  end-page: 752
  ident: CR5
  article-title: Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis
  publication-title: Mol Cell
  doi: 10.1016/j.molcel.2007.05.010
– volume: 70
  start-page: 5923
  issue: 14
  year: 2010
  end-page: 5930
  ident: CR35
  article-title: Development of a lung cancer therapeutic based on the tumor suppressor MicroRNA-34
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-10-0655
– volume: 6
  start-page: 1586
  issue: 13
  year: 2007
  end-page: 1593
  ident: CR4
  article-title: Differential regulation of microRNAs by p53 revealed by massively parallel sequencing: miR-34a is a p53 target that induces apoptosis and G1-arrest
  publication-title: Cell Cycle
  doi: 10.4161/cc.6.13.4436
– volume: 21
  start-page: 271
  issue: 3
  year: 2003
  end-page: 276
  ident: CR30
  article-title: TP53 mutation in colorectal cancer
  publication-title: Hum Mutat
  doi: 10.1002/humu.10175
– volume: 69
  start-page: 7569
  issue: 19
  year: 2009
  end-page: 7576
  ident: CR26
  article-title: MicroRNA-34a inhibits glioblastoma growth by targeting multiple oncogenes
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-09-0529
– volume: 23
  start-page: 7395
  issue: 30
  year: 2005
  end-page: 7396
  ident: CR32
  article-title: Is there a role for routine p53 testing in colorectal cancer
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2005.07.021
– volume: 16
  start-page: 1119
  issue: 4
  year: 2010
  end-page: 1128
  ident: CR21
  article-title: Frequent downregulation of miR-34 family in human ovarian cancers
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-09-2642
– volume: 275
  start-page: 44
  issue: 1
  year: 2009
  end-page: 53
  ident: CR22
  article-title: miR-34a inhibits migration and invasion by down-regulation of c-Met expression in human hepatocellular carcinoma cells
  publication-title: Cancer Lett
  doi: 10.1016/j.canlet.2008.09.035
– volume: 68
  start-page: 4123
  issue: 11
  year: 2008
  end-page: 4132
  ident: CR12
  article-title: Epigenetic silencing of microRNA-34b/c and B-cell translocation gene 4 is associated with CpG island methylation in colorectal cancer
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-08-0325
– volume: 4
  start-page: e6816
  issue: 8
  year: 2009
  ident: CR33
  article-title: MicroRNA miR-34 inhibits human pancreatic cancer tumor-initiating cells
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0006816
– volume: 7
  start-page: 2591
  issue: 16
  year: 2008
  end-page: 2600
  ident: CR16
  article-title: Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer
  publication-title: Cell Cycle
  doi: 10.4161/cc.7.16.6533
– volume: 26
  start-page: 731
  issue: 5
  year: 2007
  end-page: 743
  ident: CR6
  article-title: Transcriptional activation of miR-34a contributes to p53-mediated apoptosis
  publication-title: Mol Cell
  doi: 10.1016/j.molcel.2007.05.017
– volume: 10
  start-page: 704
  issue: 10
  year: 2009
  end-page: 714
  ident: CR3
  article-title: Causes and consequences of microRNA dysregulation in cancer
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg2634
– volume: 67
  start-page: 8433
  issue: 18
  year: 2007
  end-page: 8438
  ident: CR9
  article-title: MicroRNA-34b and MicroRNA-34c are targets of p53 and cooperate in control of cell proliferation and adhesion-independent growth
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-07-1585
– volume: 17
  start-page: 193
  issue: 2
  year: 2010
  end-page: 199
  ident: CR10
  article-title: The miR-34 family in cancer and apoptosis
  publication-title: Cell Death Differ
  doi: 10.1038/cdd.2009.56
– volume: 104
  start-page: 15472
  issue: 39
  year: 2007
  end-page: 15477
  ident: CR28
  article-title: Tumor-suppressive miR-34a induces senescence-like growth arrest through modulation of the E2F pathway in human colon cancer cells
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0707351104
– volume: 17
  start-page: 1298
  issue: 15
  year: 2007
  end-page: 1307
  ident: CR8
  article-title: p53-mediated activation of miRNA34 candidate tumor-suppressor genes
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2007.06.068
– volume: 26
  start-page: 5017
  issue: 34
  year: 2007
  end-page: 5022
  ident: CR11
  article-title: MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells
  publication-title: Oncogene
  doi: 10.1038/sj.onc.1210293
– volume: 93
  start-page: 9821
  issue: 18
  year: 1996
  end-page: 9826
  ident: CR19
  article-title: Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.93.18.9821
– volume: 30
  start-page: 1903
  issue: 11
  year: 2009
  end-page: 1909
  ident: CR25
  article-title: miR-34a as a prognostic marker of relapse in surgically resected non-small-cell lung cancer
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgp219
– year: 2002
  ident: CR20
  publication-title: TNM—Klassifikation maligner Tumoren. 6 edn. UICC International Union Against Cancer
– volume: 3
  start-page: 253
  issue: 4
  year: 2003
  end-page: 266
  ident: CR15
  article-title: The power and the promise of DNA methylation markers
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc1045
– volume: 12
  start-page: 414
  issue: 5
  year: 2007
  end-page: 418
  ident: CR2
  article-title: p53 enters the microRNA world
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2007.10.028
– volume: 319
  start-page: 1352
  issue: 5868
  year: 2008
  ident: 1030_CR17
  publication-title: Science
  doi: 10.1126/science.1140735
– volume: 23
  start-page: 7395
  issue: 30
  year: 2005
  ident: 1030_CR32
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2005.07.021
– volume: 104
  start-page: 15472
  issue: 39
  year: 2007
  ident: 1030_CR28
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0707351104
– volume: 10
  start-page: 704
  issue: 10
  year: 2009
  ident: 1030_CR3
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg2634
– volume: 3
  start-page: 253
  issue: 4
  year: 2003
  ident: 1030_CR15
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc1045
– volume: 26
  start-page: 5017
  issue: 34
  year: 2007
  ident: 1030_CR11
  publication-title: Oncogene
  doi: 10.1038/sj.onc.1210293
– volume: 128
  start-page: 683
  issue: 4
  year: 2007
  ident: 1030_CR14
  publication-title: Cell
  doi: 10.1016/j.cell.2007.01.029
– volume: 26
  start-page: 731
  issue: 5
  year: 2007
  ident: 1030_CR6
  publication-title: Mol Cell
  doi: 10.1016/j.molcel.2007.05.017
– volume: 68
  start-page: 4123
  issue: 11
  year: 2008
  ident: 1030_CR12
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-08-0325
– volume: 68
  start-page: 10128
  issue: 24
  year: 2008
  ident: 1030_CR23
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-08-2148
– volume: 17
  start-page: 236
  issue: 2
  year: 2010
  ident: 1030_CR27
  publication-title: Cell Death Differ
  doi: 10.1038/cdd.2009.109
– volume: 4
  start-page: e6816
  issue: 8
  year: 2009
  ident: 1030_CR33
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0006816
– volume: 93
  start-page: 9821
  issue: 18
  year: 1996
  ident: 1030_CR19
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.93.18.9821
– volume-title: TNM—Klassifikation maligner Tumoren. 6 edn. UICC International Union Against Cancer
  year: 2002
  ident: 1030_CR20
– volume: 3
  start-page: 415
  issue: 6
  year: 2002
  ident: 1030_CR13
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg816
– volume: 447
  start-page: 1130
  issue: 7148
  year: 2007
  ident: 1030_CR7
  publication-title: Nature
  doi: 10.1038/nature05939
– volume: 26
  start-page: 745
  issue: 5
  year: 2007
  ident: 1030_CR5
  publication-title: Mol Cell
  doi: 10.1016/j.molcel.2007.05.010
– volume: 30
  start-page: 1903
  issue: 11
  year: 2009
  ident: 1030_CR25
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgp219
– volume: 69
  start-page: 7569
  issue: 19
  year: 2009
  ident: 1030_CR26
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-09-0529
– volume: 7
  start-page: 2591
  issue: 16
  year: 2008
  ident: 1030_CR16
  publication-title: Cell Cycle
  doi: 10.4161/cc.7.16.6533
– volume: 107
  start-page: 5375
  issue: 12
  year: 2010
  ident: 1030_CR29
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0910015107
– volume: 275
  start-page: 44
  issue: 1
  year: 2009
  ident: 1030_CR22
  publication-title: Cancer Lett
  doi: 10.1016/j.canlet.2008.09.035
– volume: 105
  start-page: 13556
  issue: 36
  year: 2008
  ident: 1030_CR18
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.0803055105
– volume: 127
  start-page: 2768
  issue: 12
  year: 2010
  ident: 1030_CR24
  publication-title: Int J Cancer
  doi: 10.1002/ijc.25269
– volume: 60
  start-page: 167
  year: 2009
  ident: 1030_CR1
  publication-title: Annu Rev Med
  doi: 10.1146/annurev.med.59.053006.104707
– volume: 67
  start-page: 8433
  issue: 18
  year: 2007
  ident: 1030_CR9
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-07-1585
– volume: 17
  start-page: 193
  issue: 2
  year: 2010
  ident: 1030_CR10
  publication-title: Cell Death Differ
  doi: 10.1038/cdd.2009.56
– volume: 16
  start-page: 1119
  issue: 4
  year: 2010
  ident: 1030_CR21
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-09-2642
– volume: 6
  start-page: 1586
  issue: 13
  year: 2007
  ident: 1030_CR4
  publication-title: Cell Cycle
  doi: 10.4161/cc.6.13.4436
– volume: 17
  start-page: 1298
  issue: 15
  year: 2007
  ident: 1030_CR8
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2007.06.068
– volume: 21
  start-page: 271
  issue: 3
  year: 2003
  ident: 1030_CR30
  publication-title: Hum Mutat
  doi: 10.1002/humu.10175
– volume: 31
  start-page: 745
  issue: 4
  year: 2010
  ident: 1030_CR34
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgq033
– volume: 70
  start-page: 5923
  issue: 14
  year: 2010
  ident: 1030_CR35
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-10-0655
– volume: 12
  start-page: 414
  issue: 5
  year: 2007
  ident: 1030_CR2
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2007.10.028
– volume: 23
  start-page: 7518
  issue: 30
  year: 2005
  ident: 1030_CR31
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2005.00.471
– reference: 12042769 - Nat Rev Genet. 2002 Jun;3(6):415-28
– reference: 17320506 - Cell. 2007 Feb 23;128(4):683-92
– reference: 16186590 - J Clin Oncol. 2005 Oct 20;23(30):7395-6
– reference: 17297439 - Oncogene. 2007 Jul 26;26(34):5017-22
– reference: 19773441 - Cancer Res. 2009 Oct 1;69(19):7569-76
– reference: 12619112 - Hum Mutat. 2003 Mar;21(3):271-6
– reference: 18323444 - Science. 2008 Mar 7;319(5868):1352-5
– reference: 17540598 - Mol Cell. 2007 Jun 8;26(5):731-43
– reference: 19763153 - Nat Rev Genet. 2009 Oct;10(10):704-14
– reference: 17875987 - Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15472-7
– reference: 18768788 - Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13556-61
– reference: 18519671 - Cancer Res. 2008 Jun 1;68(11):4123-32
– reference: 19714243 - PLoS One. 2009 Aug 28;4(8):e6816
– reference: 20212154 - Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5375-80
– reference: 17996645 - Cancer Cell. 2007 Nov;12(5):414-8
– reference: 19696787 - Cell Death Differ. 2010 Feb;17(2):236-45
– reference: 17823410 - Cancer Res. 2007 Sep 15;67(18):8433-8
– reference: 8790415 - Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9821-6
– reference: 17540599 - Mol Cell. 2007 Jun 8;26(5):745-52
– reference: 19006648 - Cancer Lett. 2009 Mar 8;275(1):44-53
– reference: 19630570 - Annu Rev Med. 2009;60:167-79
– reference: 20145172 - Clin Cancer Res. 2010 Feb 15;16(4):1119-28
– reference: 20570894 - Cancer Res. 2010 Jul 15;70(14):5923-30
– reference: 17554199 - Cell Cycle. 2007 Jul 1;6(13):1586-93
– reference: 18719384 - Cell Cycle. 2008 Aug 15;7(16):2591-600
– reference: 17656095 - Curr Biol. 2007 Aug 7;17(15):1298-307
– reference: 19074879 - Cancer Res. 2008 Dec 15;68(24):10128-36
– reference: 20118199 - Carcinogenesis. 2010 Apr;31(4):745-50
– reference: 19461653 - Cell Death Differ. 2010 Feb;17(2):193-9
– reference: 21351256 - Int J Cancer. 2010 Dec 15;127(12):2768-76
– reference: 16172461 - J Clin Oncol. 2005 Oct 20;23(30):7518-28
– reference: 12671664 - Nat Rev Cancer. 2003 Apr;3(4):253-66
– reference: 17554337 - Nature. 2007 Jun 28;447(7148):1130-4
– reference: 19736307 - Carcinogenesis. 2009 Nov;30(11):1903-9
SSID ssj0021816
Score 2.4614704
Snippet The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell...
The microRNA encoding genes miR-34a and miR-34b/c represent direct p53 target genes and possess tumor suppressive properties as they mediate apoptosis, cell...
SourceID proquest
pubmed
pascalfrancis
crossref
springer
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 313
SubjectTerms Apoptosis
Biological and medical sciences
Breast Neoplasms - genetics
Cell Line, Tumor
Colorectal carcinoma
Colorectal Neoplasms - genetics
CpG Islands - genetics
DNA Methylation
DNA, Neoplasm - genetics
Female
Female genital diseases
Gene Expression Regulation, Neoplastic
Gene Silencing
Genome
Gynecology. Andrology. Obstetrics
Humans
Immunoenzyme Techniques
Inactivation
Investigative techniques, diagnostic techniques (general aspects)
Kidney Neoplasms - genetics
Kidneys
Male
Medical sciences
Medicine
Medicine & Public Health
Methylation
MicroRNAs - genetics
Mutation
Nephrology. Urinary tract diseases
Original Article
Ovarian cancer
Ovarian Neoplasms - genetics
Pancreatic cancer
Pancreatic Neoplasms - genetics
Pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Prostate cancer
Sarcoma
Sarcoma - genetics
Sarcoma - pathology
Soft Tissue Neoplasms - genetics
Soft Tissue Neoplasms - pathology
Tumors
Tumors of the urinary system
Urologic Neoplasms - genetics
SummonAdditionalLinks – databaseName: SpringerLink Contemporary (1997 - Present)
  dbid: RSV
  link: http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnR3ZatwwULRpKYHSO6mbNkyhT-2Kei1Zlh5LyLYPbSjpQd6MLFuwsPEu9m4gn5a_64x8hJCk0L7ZzOiwNNLMeC7G3qnM4dqXBdepkVwW2uOZ85ZrUTiRyqRwOgQKf82OjvTJifnex3G3g7f7YJIMN_UY7BbEex68CZAyeXqX3UNup6lew_GP36OWhSwrGCiNTLlC7jiYMm_q4gozeriyLa6L7wpa3CRxXrOWBiY0e_xf03_CHvUyJ3zqiOQpu1PVz9iDb71V_Tm7mDXBoXoNqBxjb3OqLAzzmmIeuj-2sPRwOj_mQlqwddk_Fx8dFOdwsPoMVIj6vHOrw4ZAqbDpKrWLCeB100mmbgKnNoTKTWB5hjq6rSewaSgEbDEnTOq5qWiqZE4AR2WOavJfCpAWGQasA51AiyACvGC_Zoc_D77wvqQDd6harbnzhU2ckZVJnXNepS4pVGpR50pQVnG-zKw1maCAWG2VRWBZqiQzTqOcmDkpdthWvayrlwyM8MJ6q3GfC6mTSkujs0plfqpQjY1VxOJhb3PX5zunshuLfMzUHLYkj8O7iPM0Yu_HJqsu2cffkPevEMzYgorNo8qCE9gbKCjvL4Y2R-kIZc6pMhF7O0LxRNO62rpablpSxkgsjlMcAm7B0ZRQWIipjNhuR5uXw08TSnCQROzDQIiXw9_6Na_-CXuPbXf_1skX7zXbWjeb6g27786QCpr9cB7_AI9wLtw
  priority: 102
  providerName: Springer Nature
Title Frequent concomitant inactivation of miR-34a and miR-34b/c by CpG methylation in colorectal, pancreatic, mammary, ovarian, urothelial, and renal cell carcinomas and soft tissue sarcomas
URI https://link.springer.com/article/10.1007/s00428-010-1030-5
https://www.ncbi.nlm.nih.gov/pubmed/21225432
https://www.proquest.com/docview/853505169
https://www.proquest.com/docview/1468352055
https://www.proquest.com/docview/853993314
Volume 458
WOSCitedRecordID wos000288679000007&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVPQU
  databaseName: Biological Science Database
  customDbUrl:
  eissn: 1432-2307
  dateEnd: 20171231
  omitProxy: false
  ssIdentifier: ssj0021816
  issn: 0945-6317
  databaseCode: M7P
  dateStart: 20030101
  isFulltext: true
  titleUrlDefault: http://search.proquest.com/biologicalscijournals
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: Health & Medical Collection
  customDbUrl:
  eissn: 1432-2307
  dateEnd: 20171231
  omitProxy: false
  ssIdentifier: ssj0021816
  issn: 0945-6317
  databaseCode: 7X7
  dateStart: 20030101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/healthcomplete
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: Nursing & Allied Health Database
  customDbUrl:
  eissn: 1432-2307
  dateEnd: 20171231
  omitProxy: false
  ssIdentifier: ssj0021816
  issn: 0945-6317
  databaseCode: 7RV
  dateStart: 20030101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/nahs
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: ProQuest Central
  customDbUrl:
  eissn: 1432-2307
  dateEnd: 20171231
  omitProxy: false
  ssIdentifier: ssj0021816
  issn: 0945-6317
  databaseCode: BENPR
  dateStart: 20030101
  isFulltext: true
  titleUrlDefault: https://www.proquest.com/central
  providerName: ProQuest
– providerCode: PRVAVX
  databaseName: Springer Nature
  customDbUrl:
  eissn: 1432-2307
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0021816
  issn: 0945-6317
  databaseCode: RSV
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: https://link.springer.com/search?facet-content-type=%22Journal%22
  providerName: Springer Nature
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpR1db9Mw0IINISTE54AwqIzEE9RaGif-eEIwrfAAVVVg6lvkOLFUqUtK0k7aT-Pfced8TBNsL7xYic6OHfvsu_N9EfJWSAtzn2dMJTpmcaYc7DlnmOKZ5UkcZVZ5R-GvcjZTy6Wed7Y5TWdW2Z-J_qDOK4t35EdAVoBYT4T-sPnFMGkUKle7DBq3yf4EWWNAZ7k4HeQtIF5eVanjhAmgk71SM2xjiGJoZjRNADRnyRWydH9jGpgh16a2-Bfv-Zfe1JOj6cP__JFH5EHHh9KPLeI8JreK8gm5-63TtD8lv6e1N7LeUhCY4cMrzDZMVyX6QbS3uLRy9Gy1YDw21JR595wdWZpd0OPNZ4rJqS9aUztoSDE8Nh6vZj2mcAS13Kod0zPj3efGtDoHud2UY7qr0S1svcKa-OW6wKGiioFaTH1Uok2ThzRAROjW4w5tAISAA_JzevLj-Avr0jwwC-LWllmXmcjquNCJtdaJxEaZSAzIYRHwL9bl0hgtOTrJKiMMAPNcRFJbBbyjtDF_RvbKqixeEKq548YZBSuexSoqVKyVLIR0EwGibSgCEvarnNouBjqm4linQ_Rmjxhp6N95mCYBeTc02bQBQG6qPLqCOkMLTEAPYgwM4LBHirQ7LJp0wIiAvBmgsMtxXk1ZVLsGBTRklcMEuqDX1FEYZJjzSRyQ5y2WXnY_iTDoQRSQ9z3aXnZ_7d-8vHGwh-Ree7-O9nivyN623hWvyR17Dqtej_xOxHIpfalGZP_TyWy-GKF17RzKxffTP5cmPrg
linkProvider ProQuest
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1R3bbtMw9GgMxJAQ90EZDCPBCzRaajuJ_YAQGpRN6yqEhtS34DiJVKlLStMO9aP4AP6Oc5yk1QTb2x54S3Ts2HHONecG8CqMLJ59mngq0NKTicqR5nLjKZFYEUieWOUShQfRcKhGI_1lA361uTAUVtnyRMeo09LSP_I9FCsorHuhfj_94VHTKHKuth00aqw4ypY_0WKr3h1-xM_7mvP-p5P9A69pKuBZVO7nns0Tw62WmQ6stXkYWJ6EgUGtn6O0tHkaGaMjQSmZyoQGgWka8khbhZpKZKXA516D68jGI7L1otHavkNh6VyjWgZeiHK5daL6dc1SKgVNoRBIVl5wTgzenpoKv0het9L4l677l5_Wib_-3f_s4O7BnUbPZh9qwrgPG1nxAG4eN5EED-F3f-aCyOfMlgW-yJi6KbNxQXke9V9qVubsdPzVE9IwU6TNdbJnWbJk-9PPjJpvL-tQQpzIqPw3iQ8z6TJksbU2brvs1Lj0wC4rzwxSe9FlixmlvU3GNJKePMtoq-RCYZZaOxUUs-UgFQpJNne0wSoEEeARfLuSg9uGzaIssifAtMiFyY1CDEuk4pmSWkVZGOW9EE13P-yA32JVbJsa79RqZBKvqlM7RIx9dy_8OOjAm9WUaV3g5LLBu-dQdTWDCy3RTMMN7LRIGDfMsIpXGNiBlysocjE6V1Nk5aIiA5RMAT_AJdgFYxQVURaiJzvwuKaK9fI9TkUdeAfetmSyXv7Ct3l66WZfwNbByfEgHhwOj3bgVu1LoNjDZ7A5ny2y53DDniEGzHYdF2Dw_aqp5w_PdJaT
linkToPdf http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1R3bbtMw9Gh0aEJCjDtlMIwEL9Coqe0k9gNCY1th2qiqiUl7C46TSJW6pDTtUD9tf8c5uU0TbG974C3RsWPHOdecG8A7P7B49nHkKE9LR0YqRZpLjaNEZIUneWRVmSh8FIxG6vRUj9fgosmFobDKhieWjDrOLf0j76NYQWE98HU_raMixnvDz7NfDjWQIkdr002jwpDDZPUbrbfi08Eefur3nA_3f-x-c-oGA45FRX_h2DQy3GqZaM9am_qe5ZHvGbQAOEpOm8aBMToQlJ6pjG8QGMc-D7RVqLUEVgp87h1YD1DHkB1Y_7I_Gh-31h6KztJRqqXn-CilG5eqW1UwpcLQFBiBROZ4V4Ti_Zkp8PukVWONf2m-f3ltS2E43PyPj_EhPKg1cLZTkcwjWEuyx7DxvY4xeAIXw3kZXr5gNs_wpSbUZ5lNMsoAqf5fszxlZ5NjR0jDTBbX11HfsmjFdmdfGbXlXlVBhjiRUWFwEixm2mPIfCs93fbYmSkTB3ssPzfIB7IeW84pIW46oZH05HlCWyXnCrPU9CmjaK4SUqD4ZIuSaliBIAI8hZNbObhn0MnyLHkBTItUmNQoxLZIKp4oqVWQ-EE68NGod_0uuA2Ghbau_k5NSKZhW7e6RMrQLe-FG3pd-NBOmVWlT24avH0FbdsZXGiJBhxuYKtByLBmk0XYYmMX3rZQ5G90riZL8mVBpikZCa6HS7BrxigqryzEQHbheUUhl8sPOJV74F342JDM5fLXvs3LGzf7BjaQaMKjg9HhFtyrnAwUlPgKOov5MnkNd-05IsB8u2YJDH7eNvn8AeS-oLM
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Frequent+concomitant+inactivation+of+miR-34a+and+miR-34b%2Fc+by+CpG+methylation+in+colorectal%2C+pancreatic%2C+mammary%2C+ovarian%2C+urothelial%2C+and+renal+cell+carcinomas+and+soft+tissue+sarcomas&rft.jtitle=Virchows+Archiv+%3A+an+international+journal+of+pathology&rft.au=Vogt%2C+Markus&rft.au=Munding%2C+Johanna&rft.au=Gr%C3%BCner%2C+Martha&rft.au=Liffers%2C+Sven-thorsten&rft.date=2011-03-01&rft.pub=Springer+Nature+B.V&rft.issn=0945-6317&rft.eissn=1432-2307&rft.volume=458&rft.issue=3&rft.spage=313&rft_id=info:doi/10.1007%2Fs00428-010-1030-5&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=2274987111
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0945-6317&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0945-6317&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0945-6317&client=summon