Your browser doesn't support javascript.
loading
Posttranscriptional methylation of transfer and ribosomal RNA in stress response pathways, cell differentiation, and cancer.
Popis, Martyna C; Blanco, Sandra; Frye, Michaela.
Affiliation
  • Popis MC; Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, United Kingdom.
  • Blanco S; Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, United Kingdom.
  • Frye M; Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, United Kingdom.
Curr Opin Oncol ; 28(1): 65-71, 2016 Jan.
Article in En | MEDLINE | ID: mdl-26599292
PURPOSE OF REVIEW: Significant advances have been made in understanding the functional roles of evolutionarily conserved chemical modifications in RNA. By focusing on cytosine-5 methylation, we will highlight the latest insight into the mechanisms how posttranscriptional methylation contributes to cell fate decisions, with implications for cancer development. RECENT FINDINGS: Several mutations in RNA-modifying enzymes have been identified to cause complex human diseases, and linked posttranscriptional modifications to fundamental cellular processes. Distinct posttranscriptional modifications are implicated in the regulation of stem cell maintenance and cellular differentiation. The dynamic deposition of a methyl mark into noncoding RNAs modulates the adaptive cellular responses to stress and alterations of methylation levels may lead to cancer. SUMMARY: Posttranscriptional modifications such as cytosine-5 methylation are dynamically regulated and may influence tumour development, maintenance, and progression.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress, Physiological / RNA, Ribosomal / RNA Processing, Post-Transcriptional / Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Curr Opin Oncol Journal subject: NEOPLASIAS Year: 2016 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress, Physiological / RNA, Ribosomal / RNA Processing, Post-Transcriptional / Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Curr Opin Oncol Journal subject: NEOPLASIAS Year: 2016 Document type: Article Affiliation country: Country of publication: