Non-coding RNA networks in cancer

Key Points Non-coding RNAs (ncRNAs) participate in complex networks of interactions with other nucleic acids and proteins that often have wide-reaching effects on cell biology. The mechanisms by which ncRNAs work and/or function are routinely dysregulated in various cancers. Dysregulation of ncRNA i...

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Published in:Nature reviews. Cancer Vol. 18; no. 1; pp. 5 - 18
Main Authors: Anastasiadou, Eleni, Jacob, Leni S., Slack, Frank J.
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01.01.2018
Nature Publishing Group
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ISSN:1474-175X, 1474-1768, 1474-1768
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Abstract Key Points Non-coding RNAs (ncRNAs) participate in complex networks of interactions with other nucleic acids and proteins that often have wide-reaching effects on cell biology. The mechanisms by which ncRNAs work and/or function are routinely dysregulated in various cancers. Dysregulation of ncRNA interactions within cancer molecular pathways contributes to cancer and reveals important new targets for intervention. In cancer, disruptions in ncRNA networks often do not involve just mutations that cause a gross gain-of-function or loss-of-function of a given ncRNA but can also involve mutations that change the sequence and downstream targets of that ncRNA. Non-coding RNAs (ncRNAs) are functional molecules that regulate physiological programmes in developmental and disease contexts. This Review article discusses the complex networks of interactions that ncRNAs engage in and how these confer oncogenic or tumour-suppressive effects in cancer. Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from 'junk' transcriptional products to functional regulatory molecules that mediate cellular processes including chromatin remodelling, transcription, post-transcriptional modifications and signal transduction. The networks in which ncRNAs engage can influence numerous molecular targets to drive specific cell biological responses and fates. Consequently, ncRNAs act as key regulators of physiological programmes in developmental and disease contexts. Particularly relevant in cancer, ncRNAs have been identified as oncogenic drivers and tumour suppressors in every major cancer type. Thus, a deeper understanding of the complex networks of interactions that ncRNAs coordinate would provide a unique opportunity to design better therapeutic interventions.
AbstractList Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from ‘junk’ transcriptional products to functional regulatory molecules that mediate cellular processes including chromatin remodelling, transcription, post-transcriptional modifications and signal transduction. The networks in which ncRNAs engage can influence numerous molecular targets to drive specific cell biological responses and fates. Consequently, ncRNAs act as key regulators of physiological programmes in developmental and disease contexts. Particularly relevant in cancer, ncRNAs have been identified as oncogenic drivers and tumour suppressors in every major cancer type. Thus, a deeper understanding of the complex networks of interactions that ncRNAs coordinate would provide a unique opportunity to design better therapeutic interventions.
Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from 'junk' transcriptional products to functional regulatory molecules that mediate cellular processes including chromatin remodelling, transcription, post-transcriptional modifications and signal transduction. The networks in which ncRNAs engage can influence numerous molecular targets to drive specific cell biological responses and fates. Consequently, ncRNAs act as key regulators of physiological programmes in developmental and disease contexts. Particularly relevant in cancer, ncRNAs have been identified as oncogenic drivers and tumour suppressors in every major cancer type. Thus, a deeper understanding of the complex networks of interactions that ncRNAs coordinate would provide a unique opportunity to design better therapeutic interventions.Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from 'junk' transcriptional products to functional regulatory molecules that mediate cellular processes including chromatin remodelling, transcription, post-transcriptional modifications and signal transduction. The networks in which ncRNAs engage can influence numerous molecular targets to drive specific cell biological responses and fates. Consequently, ncRNAs act as key regulators of physiological programmes in developmental and disease contexts. Particularly relevant in cancer, ncRNAs have been identified as oncogenic drivers and tumour suppressors in every major cancer type. Thus, a deeper understanding of the complex networks of interactions that ncRNAs coordinate would provide a unique opportunity to design better therapeutic interventions.
Key Points Non-coding RNAs (ncRNAs) participate in complex networks of interactions with other nucleic acids and proteins that often have wide-reaching effects on cell biology. The mechanisms by which ncRNAs work and/or function are routinely dysregulated in various cancers. Dysregulation of ncRNA interactions within cancer molecular pathways contributes to cancer and reveals important new targets for intervention. In cancer, disruptions in ncRNA networks often do not involve just mutations that cause a gross gain-of-function or loss-of-function of a given ncRNA but can also involve mutations that change the sequence and downstream targets of that ncRNA. Non-coding RNAs (ncRNAs) are functional molecules that regulate physiological programmes in developmental and disease contexts. This Review article discusses the complex networks of interactions that ncRNAs engage in and how these confer oncogenic or tumour-suppressive effects in cancer. Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from 'junk' transcriptional products to functional regulatory molecules that mediate cellular processes including chromatin remodelling, transcription, post-transcriptional modifications and signal transduction. The networks in which ncRNAs engage can influence numerous molecular targets to drive specific cell biological responses and fates. Consequently, ncRNAs act as key regulators of physiological programmes in developmental and disease contexts. Particularly relevant in cancer, ncRNAs have been identified as oncogenic drivers and tumour suppressors in every major cancer type. Thus, a deeper understanding of the complex networks of interactions that ncRNAs coordinate would provide a unique opportunity to design better therapeutic interventions.
Audience Academic
Author Slack, Frank J.
Jacob, Leni S.
Anastasiadou, Eleni
Author_xml – sequence: 1
  givenname: Eleni
  surname: Anastasiadou
  fullname: Anastasiadou, Eleni
  organization: Department of Pathology, Harvard Medical School Initiative for RNA Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School
– sequence: 2
  givenname: Leni S.
  surname: Jacob
  fullname: Jacob, Leni S.
  organization: Department of Pathology, Harvard Medical School Initiative for RNA Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School
– sequence: 3
  givenname: Frank J.
  surname: Slack
  fullname: Slack, Frank J.
  email: fslack@bidmc.harvard.edu
  organization: Department of Pathology, Harvard Medical School Initiative for RNA Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29170536$$D View this record in MEDLINE/PubMed
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These authors contributed equally to this work.
E.A. and L.S.J. researched the data for the article. E.A., L.S.J. and F.J.S. provided substantial contributions to discussions of its content, wrote the article and undertook review and/or editing of the manuscript before submission.
Author contributions
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pubmed_primary_29170536
crossref_citationtrail_10_1038_nrc_2017_99
crossref_primary_10_1038_nrc_2017_99
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PublicationCentury 2000
PublicationDate 2018-01-01
PublicationDateYYYYMMDD 2018-01-01
PublicationDate_xml – month: 01
  year: 2018
  text: 2018-01-01
  day: 01
PublicationDecade 2010
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle Nature reviews. Cancer
PublicationTitleAbbrev Nat Rev Cancer
PublicationTitleAlternate Nat Rev Cancer
PublicationYear 2018
Publisher Nature Publishing Group UK
Nature Publishing Group
Publisher_xml – name: Nature Publishing Group UK
– name: Nature Publishing Group
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Snippet Key Points Non-coding RNAs (ncRNAs) participate in complex networks of interactions with other nucleic acids and proteins that often have wide-reaching effects...
Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from 'junk'...
Thousands of unique non-coding RNA (ncRNA) sequences exist within cells. Work from the past decade has altered our perception of ncRNAs from ‘junk’...
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proquest
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pubmed
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SourceType Open Access Repository
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Publisher
StartPage 5
SubjectTerms 631/208/200
631/337/1645
631/337/384
631/67/395
631/80/86
Animals
Biomedicine
Cancer
Cancer Research
Carcinogenesis
Chromatin remodeling
Gene expression
Genetic aspects
Health aspects
Humans
Innovations
Molecular targeted therapy
Neoplasms - genetics
Non-coding RNA
Post-transcription
review-article
RNA
RNA Processing, Post-Transcriptional - genetics
RNA, Untranslated - genetics
Signal transduction
Signal Transduction - genetics
Therapeutic applications
Transcription, Genetic - genetics
Transduction
Tumors
Title Non-coding RNA networks in cancer
URI https://link.springer.com/article/10.1038/nrc.2017.99
https://www.ncbi.nlm.nih.gov/pubmed/29170536
https://www.proquest.com/docview/1978779043
https://www.proquest.com/docview/1968442826
https://pubmed.ncbi.nlm.nih.gov/PMC6337726
Volume 18
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