Emerging roles of long non‐coding RNA in cancer

Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next‐generation sequencing technologies have provided accumulating evidence of dys...

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Vydáno v:Cancer science Ročník 109; číslo 7; s. 2093 - 2100
Hlavní autoři: Sanchez Calle, Anna, Kawamura, Yumi, Yamamoto, Yusuke, Takeshita, Fumitaka, Ochiya, Takahiro
Médium: Journal Article
Jazyk:angličtina
Vydáno: England John Wiley & Sons, Inc 01.07.2018
John Wiley and Sons Inc
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ISSN:1347-9032, 1349-7006, 1349-7006
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Abstract Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next‐generation sequencing technologies have provided accumulating evidence of dysregulated lncRNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post‐transcriptional processes, aberrant expression of lncRNA may have repercussions in cell proliferation, tumor progression or metastasis. lncRNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well‐established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer‐associated lncRNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations. lncRNAs involved in tumor plasticity. Aberrantly expressed lncRNAs may have an important impact in the EMT‐MET processes by interacting with diverse signaling cascades.
AbstractList Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non-coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next-generation sequencing technologies have provided accumulating evidence of dysregulated lncRNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post-transcriptional processes, aberrant expression of lncRNA may have repercussions in cell proliferation, tumor progression or metastasis. lncRNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well-established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer-associated lncRNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations.
Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lnc RNA ), increasing attention has been paid to these transcripts. The applied next‐generation sequencing technologies have provided accumulating evidence of dysregulated lnc RNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post‐transcriptional processes, aberrant expression of lnc RNA may have repercussions in cell proliferation, tumor progression or metastasis. lnc RNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well‐established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer‐associated lnc RNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations.
Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next‐generation sequencing technologies have provided accumulating evidence of dysregulated lncRNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post‐transcriptional processes, aberrant expression of lncRNA may have repercussions in cell proliferation, tumor progression or metastasis. lncRNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well‐established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer‐associated lncRNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations. lncRNAs involved in tumor plasticity. Aberrantly expressed lncRNAs may have an important impact in the EMT‐MET processes by interacting with diverse signaling cascades.
Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non-coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next-generation sequencing technologies have provided accumulating evidence of dysregulated lncRNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post-transcriptional processes, aberrant expression of lncRNA may have repercussions in cell proliferation, tumor progression or metastasis. lncRNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well-established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer-associated lncRNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations.Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non-coding RNA (lncRNA), increasing attention has been paid to these transcripts. The applied next-generation sequencing technologies have provided accumulating evidence of dysregulated lncRNA in cancer. The implication of this finding can be seen in many forms and at multiple levels. With impacts ranging from integrating chromatin remodeling complexes to regulating transcription and post-transcriptional processes, aberrant expression of lncRNA may have repercussions in cell proliferation, tumor progression or metastasis. lncRNA may act as enhancers, scaffolds or decoys by physically interacting with other RNA species or proteins, resulting in a direct impact on cell signaling cascades. Even though their functional classification is well-established in the context of cancer, clearer characterization in terms of their phenotypic outputs is needed to optimize and identify suitable candidates that enable the development of new therapeutic strategies and the design of novel diagnostic approaches. The present article aims to outline different cancer-associated lncRNA according to their contribution to tumor suppression or tumor promotion based on their most current functional annotations.
Author Sanchez Calle, Anna
Kawamura, Yumi
Yamamoto, Yusuke
Takeshita, Fumitaka
Ochiya, Takahiro
AuthorAffiliation 1 Division of Molecular and Cellular Medicine National Cancer Center Research Institute Tokyo Japan
3 Department of Functional Analysis FIOC National Cancer Center Research Institute Tokyo Japan
4 Institute of Medical Science Tokyo Medical University Tokyo Japan
2 Ph.D. Program in Human Biology School of Integrative and Global Majors University of Tsukuba Tsukuba Japan
AuthorAffiliation_xml – name: 2 Ph.D. Program in Human Biology School of Integrative and Global Majors University of Tsukuba Tsukuba Japan
– name: 1 Division of Molecular and Cellular Medicine National Cancer Center Research Institute Tokyo Japan
– name: 3 Department of Functional Analysis FIOC National Cancer Center Research Institute Tokyo Japan
– name: 4 Institute of Medical Science Tokyo Medical University Tokyo Japan
Author_xml – sequence: 1
  givenname: Anna
  orcidid: 0000-0002-1127-5822
  surname: Sanchez Calle
  fullname: Sanchez Calle, Anna
  organization: National Cancer Center Research Institute
– sequence: 2
  givenname: Yumi
  orcidid: 0000-0001-8386-4645
  surname: Kawamura
  fullname: Kawamura, Yumi
  organization: University of Tsukuba
– sequence: 3
  givenname: Yusuke
  surname: Yamamoto
  fullname: Yamamoto, Yusuke
  organization: National Cancer Center Research Institute
– sequence: 4
  givenname: Fumitaka
  surname: Takeshita
  fullname: Takeshita, Fumitaka
  organization: National Cancer Center Research Institute
– sequence: 5
  givenname: Takahiro
  orcidid: 0000-0002-0776-9918
  surname: Ochiya
  fullname: Ochiya, Takahiro
  email: tochiya@ncc.go.jp
  organization: Tokyo Medical University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29774630$$D View this record in MEDLINE/PubMed
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Copyright 2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
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Keywords tumor suppressors
long non-coding RNA
tumor drivers
tumor plasticity
epithelial-to-mesenchymal transition
Language English
License Attribution-NonCommercial
2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
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Snippet Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lncRNA), increasing...
Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non‐coding RNA (lnc RNA ),...
Since comprehensive analysis of the mammalian genome revealed that the majority of genomic products are transcribed in long non-coding RNA (lncRNA), increasing...
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StartPage 2093
SubjectTerms Androgens
Animals
Apoptosis
Autophagy
Bladder cancer
Breast cancer
Cancer
Cell cycle
Cell growth
Cell proliferation
Chromatin remodeling
Colorectal cancer
Deoxyribonucleic acid
DNA
DNA methylation
Enhancers
Epigenetics
epithelial‐to‐mesenchymal transition
Gene expression
Genomes
Humans
long non‐coding RNA
Metastases
Neoplasms - genetics
Ovarian cancer
Prostate cancer
Proteins
Review
Ribonucleic acid
RNA
RNA, Long Noncoding - genetics
Transcription
tumor drivers
tumor plasticity
Tumor suppression
tumor suppressors
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Title Emerging roles of long non‐coding RNA in cancer
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