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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| Vydané v: | Cancer science Ročník 109; číslo 7; s. 2093 - 2100 |
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| Hlavní autori: | , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
England
John Wiley & Sons, Inc
01.07.2018
John Wiley and Sons Inc |
| Predmet: | |
| ISSN: | 1347-9032, 1349-7006, 1349-7006 |
| On-line prístup: | Získať plný text |
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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. |
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| 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.
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 (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.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. 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. 2018. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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| 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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