HMGB1 correlates with angiogenesis and poor prognosis of perihilar cholangiocarcinoma via elevating VEGFR2 of vessel endothelium

Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical complexity and low possibility of radical surgery, whi...

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Vydáno v:Oncogene Ročník 38; číslo 6; s. 868 - 880
Hlavní autoři: Xu, Yun-Fei, Liu, Zeng-Li, Pan, Chang, Yang, Xiao-Qing, Ning, Shang-Lei, Liu, Hong-Da, Guo, Sen, Yu, Jin-Ming, Zhang, Zong-Li
Médium: Journal Article
Jazyk:angličtina
Vydáno: London Nature Publishing Group UK 01.02.2019
Nature Publishing Group
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ISSN:0950-9232, 1476-5594, 1476-5594
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Abstract Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical complexity and low possibility of radical surgery, which resulted in the difficulty of specimen obtainment. To screen and identify new biomarkers in PHCCA, we constructed a retrospective cohort with 121 PHCCA patients and a prospective cohort consisting of 64 PHCCA patients, and screened the candidate biomarkers by immunohistochemistry and quantified PCR. In our study, expression of high mobility group box 1 (HMGB1) was demonstrated to be significantly associated with microvascular density (MVD) and unfavorable prognosis of PHCCA in both retrospective and prospective study. Moreover, HMGB1 concentrations in bile and serum of PHCCA patients and healthy controls were detected and compared. Postoperative serum HMGB1 and reflux cholangitis indicated recurrence and unfavorable prognosis of PHCCA. With experiments in vitro and in vivo, we demonstrated that intracellular HMGB1 could be released from PHCCA cells and induce invasion and angiogenesis with LPS stimulation. VEGFR2 expression in vessel endothelial cells was upregulated by the released HMGB1 from PHCCA, resulting in the ectopic angiogenesis. In conclusion, intracellular HMGB1 could be released from PHCCA cells and promote angiogenesis via elevating VEGFR2 in vessel endothelial cells. High expression of HMGB1 was associated with MVD and poor prognosis in clinical analyzation. Postoperative serum HMGB1 and cholangitis could predict high recurrence and unfavorable prognosis.
AbstractList Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical complexity and low possibility of radical surgery, which resulted in the difficulty of specimen obtainment. To screen and identify new biomarkers in PHCCA, we constructed a retrospective cohort with 121 PHCCA patients and a prospective cohort consisting of 64 PHCCA patients, and screened the candidate biomarkers by immunohistochemistry and quantified PCR. In our study, expression of high mobility group box 1 (HMGB1) was demonstrated to be significantly associated with microvascular density (MVD) and unfavorable prognosis of PHCCA in both retrospective and prospective study. Moreover, HMGB1 concentrations in bile and serum of PHCCA patients and healthy controls were detected and compared. Postoperative serum HMGB1 and reflux cholangitis indicated recurrence and unfavorable prognosis of PHCCA. With experiments in vitro and in vivo, we demonstrated that intracellular HMGB1 could be released from PHCCA cells and induce invasion and angiogenesis with LPS stimulation. VEGFR2 expression in vessel endothelial cells was upregulated by the released HMGB1 from PHCCA, resulting in the ectopic angiogenesis. In conclusion, intracellular HMGB1 could be released from PHCCA cells and promote angiogenesis via elevating VEGFR2 in vessel endothelial cells. High expression of HMGB1 was associated with MVD and poor prognosis in clinical analyzation. Postoperative serum HMGB1 and cholangitis could predict high recurrence and unfavorable prognosis.
Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical complexity and low possibility of radical surgery, which resulted in the difficulty of specimen obtainment. To screen and identify new biomarkers in PHCCA, we constructed a retrospective cohort with 121 PHCCA patients and a prospective cohort consisting of 64 PHCCA patients, and screened the candidate biomarkers by immunohistochemistry and quantified PCR. In our study, expression of high mobility group box 1 (HMGB1) was demonstrated to be significantly associated with microvascular density (MVD) and unfavorable prognosis of PHCCA in both retrospective and prospective study. Moreover, HMGB1 concentrations in bile and serum of PHCCA patients and healthy controls were detected and compared. Postoperative serum HMGB1 and reflux cholangitis indicated recurrence and unfavorable prognosis of PHCCA. With experiments in vitro and in vivo, we demonstrated that intracellular HMGB1 could be released from PHCCA cells and induce invasion and angiogenesis with LPS stimulation. VEGFR2 expression in vessel endothelial cells was upregulated by the released HMGB1 from PHCCA, resulting in the ectopic angiogenesis. In conclusion, intracellular HMGB1 could be released from PHCCA cells and promote angiogenesis via elevating VEGFR2 in vessel endothelial cells. High expression of HMGB1 was associated with MVD and poor prognosis in clinical analyzation. Postoperative serum HMGB1 and cholangitis could predict high recurrence and unfavorable prognosis.Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical complexity and low possibility of radical surgery, which resulted in the difficulty of specimen obtainment. To screen and identify new biomarkers in PHCCA, we constructed a retrospective cohort with 121 PHCCA patients and a prospective cohort consisting of 64 PHCCA patients, and screened the candidate biomarkers by immunohistochemistry and quantified PCR. In our study, expression of high mobility group box 1 (HMGB1) was demonstrated to be significantly associated with microvascular density (MVD) and unfavorable prognosis of PHCCA in both retrospective and prospective study. Moreover, HMGB1 concentrations in bile and serum of PHCCA patients and healthy controls were detected and compared. Postoperative serum HMGB1 and reflux cholangitis indicated recurrence and unfavorable prognosis of PHCCA. With experiments in vitro and in vivo, we demonstrated that intracellular HMGB1 could be released from PHCCA cells and induce invasion and angiogenesis with LPS stimulation. VEGFR2 expression in vessel endothelial cells was upregulated by the released HMGB1 from PHCCA, resulting in the ectopic angiogenesis. In conclusion, intracellular HMGB1 could be released from PHCCA cells and promote angiogenesis via elevating VEGFR2 in vessel endothelial cells. High expression of HMGB1 was associated with MVD and poor prognosis in clinical analyzation. Postoperative serum HMGB1 and cholangitis could predict high recurrence and unfavorable prognosis.
Audience Academic
Author Liu, Zeng-Li
Xu, Yun-Fei
Ning, Shang-Lei
Liu, Hong-Da
Pan, Chang
Guo, Sen
Yang, Xiao-Qing
Zhang, Zong-Li
Yu, Jin-Ming
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  organization: Department of General Surgery, Qilu Hospital of Shandong University
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  surname: Liu
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  organization: Department of Pathology, Qianfoshan Hospital of Shandong University
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30177842$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1158/0008-5472.CAN-05-2217
10.1053/j.gastro.2013.10.013
10.1002/path.1031
10.1038/cr.2017.51
10.2119/molmed.2015.00087
10.1016/S0002-9440(10)62296-1
10.1002/path.2391
10.1053/j.gastro.2013.01.001
10.1089/ars.2010.3356
10.1038/sj.bjc.6604129
10.1152/ajpregu.00184.2009
10.1038/nature18317
10.1172/JCI76887
10.1038/onc.2012.49
10.1016/S0140-6736(13)61903-0
10.3748/wjg.v21.i11.3256
10.1097/01.sla.0000251366.62632.d3
10.1016/j.bbagrm.2009.09.008
10.1016/j.bbrc.2014.02.050
10.1128/MCB.23.8.2991-2998.2003
10.4161/auto.23691
10.1155/2013/157103
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References Q Zhang (485_CR7) 2013; 9
DC Avgousti (485_CR8) 2016; 535
D Wu (485_CR13) 2008; 216
N Razumilava (485_CR1) 2014; 383
R Kang (485_CR24) 2017; 27
S Rizvi (485_CR4) 2017; 15
R Yang (485_CR22) 2009; 297
I Poser (485_CR9) 2003; 23
S Rizvi (485_CR2) 2013; 145
H Kuniyasu (485_CR10) 2002; 196
M Gnanasekar (485_CR12) 2013; 2013
JR van Beijnum (485_CR19) 2013; 32
H Yang (485_CR20) 2015; 21
KD Lillemoe (485_CR3) 2003; 14
ML DeOliveira (485_CR5) 2007; 245
YF Xu (485_CR17) 2014; 446
D Yoshikawa (485_CR16) 2008; 98
M Stros (485_CR6) 2010; 1799
YF Xu (485_CR14) 2015; 21
H Kuniyasu (485_CR11) 2005; 166
P Huebener (485_CR21) 2015; 125
D Tang (485_CR23) 2011; 14
D Sia (485_CR15) 2013; 144
J Dixelius (485_CR18) 2006; 66
40730916 - Oncogene. 2025 Jul 29. doi: 10.1038/s41388-025-03514-w.
References_xml – volume: 66
  start-page: 2089
  year: 2006
  ident: 485_CR18
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-05-2217
– volume: 145
  start-page: 1215
  year: 2013
  ident: 485_CR2
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2013.10.013
– volume: 196
  start-page: 163
  year: 2002
  ident: 485_CR10
  publication-title: J Pathol
  doi: 10.1002/path.1031
– volume: 27
  start-page: 916
  year: 2017
  ident: 485_CR24
  publication-title: Cell Res
  doi: 10.1038/cr.2017.51
– volume: 21
  start-page: S6
  issue: Suppl 1
  year: 2015
  ident: 485_CR20
  publication-title: Mol Med
  doi: 10.2119/molmed.2015.00087
– volume: 14
  start-page: 208
  year: 2003
  ident: 485_CR3
  publication-title: Semin Gastrointest Dis
– volume: 166
  start-page: 751
  year: 2005
  ident: 485_CR11
  publication-title: Am J Pathol
  doi: 10.1016/S0002-9440(10)62296-1
– volume: 216
  start-page: 167
  year: 2008
  ident: 485_CR13
  publication-title: J Pathol
  doi: 10.1002/path.2391
– volume: 144
  start-page: 829
  year: 2013
  ident: 485_CR15
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2013.01.001
– volume: 14
  start-page: 1315
  year: 2011
  ident: 485_CR23
  publication-title: Antioxid Redox Signal
  doi: 10.1089/ars.2010.3356
– volume: 98
  start-page: 418
  year: 2008
  ident: 485_CR16
  publication-title: Br J Cancer
  doi: 10.1038/sj.bjc.6604129
– volume: 297
  start-page: R362
  year: 2009
  ident: 485_CR22
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00184.2009
– volume: 535
  start-page: 173
  year: 2016
  ident: 485_CR8
  publication-title: Nature
  doi: 10.1038/nature18317
– volume: 125
  start-page: 539
  year: 2015
  ident: 485_CR21
  publication-title: J Clin Invest
  doi: 10.1172/JCI76887
– volume: 32
  start-page: 363
  year: 2013
  ident: 485_CR19
  publication-title: Oncogene
  doi: 10.1038/onc.2012.49
– volume: 383
  start-page: 2168
  year: 2014
  ident: 485_CR1
  publication-title: Lancet
  doi: 10.1016/S0140-6736(13)61903-0
– volume: 15
  start-page: 95
  year: 2017
  ident: 485_CR4
  publication-title: Nat Rev Clin Oncol
– volume: 21
  start-page: 3256
  year: 2015
  ident: 485_CR14
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v21.i11.3256
– volume: 245
  start-page: 755
  year: 2007
  ident: 485_CR5
  publication-title: Ann Surg
  doi: 10.1097/01.sla.0000251366.62632.d3
– volume: 1799
  start-page: 101
  year: 2010
  ident: 485_CR6
  publication-title: Biochim Biophys Acta
  doi: 10.1016/j.bbagrm.2009.09.008
– volume: 446
  start-page: 54
  year: 2014
  ident: 485_CR17
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2014.02.050
– volume: 23
  start-page: 2991
  year: 2003
  ident: 485_CR9
  publication-title: Mol Cell Biol
  doi: 10.1128/MCB.23.8.2991-2998.2003
– volume: 9
  start-page: 451
  year: 2013
  ident: 485_CR7
  publication-title: Autophagy
  doi: 10.4161/auto.23691
– volume: 2013
  start-page: 157103
  year: 2013
  ident: 485_CR12
  publication-title: Prostate Cancer
  doi: 10.1155/2013/157103
– reference: 40730916 - Oncogene. 2025 Jul 29. doi: 10.1038/s41388-025-03514-w.
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Snippet Perihilar cholangiocarcinoma (PHCCA) is the most common type of cholangiocarcinoma with low resection rate and high morbidity. The study of PHCCA biomarkers...
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SubjectTerms 631/67
692/53/2422
Angiogenesis
Apoptosis
Bile
Bile Duct Neoplasms - blood
Bile Duct Neoplasms - mortality
Bile Duct Neoplasms - surgery
Bile ducts
Biliary tract cancer
Biological markers
Biomarkers
Cancer therapies
Care and treatment
Cell Biology
Cholangiocarcinoma
Cholangitis
Chromosomal proteins
Clinical significance
Development and progression
Disease-Free Survival
Endothelial cells
Endothelial Cells - metabolism
Endothelial Cells - pathology
Endothelium
Epidermal growth factor receptors
Female
Gene expression
Genetic aspects
Health aspects
HMGB1 protein
HMGB1 Protein - blood
Human Genetics
Humans
Immune response
Immunohistochemistry
Internal Medicine
Intracellular
Klatskin Tumor - blood
Klatskin Tumor - mortality
Klatskin Tumor - surgery
Lipopolysaccharides
Male
Medical prognosis
Medicine
Medicine & Public Health
Metastasis
Microvasculature
Morbidity
Multivariate analysis
Neoplasm Proteins - blood
Neovascularization, Pathologic - blood
Neovascularization, Pathologic - mortality
Neovascularization, Pathologic - surgery
Oncology
Patients
Prognosis
Prospective Studies
Surgery
Survival Rate
Transcription factors
Vascular endothelial growth factor
Title HMGB1 correlates with angiogenesis and poor prognosis of perihilar cholangiocarcinoma via elevating VEGFR2 of vessel endothelium
URI https://link.springer.com/article/10.1038/s41388-018-0485-8
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Volume 38
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