4.2 Review

Posttranscriptional methylation of transfer and ribosomal RNA in stress response pathways, cell differentiation, and cancer

期刊

CURRENT OPINION IN ONCOLOGY
卷 28, 期 1, 页码 65-71

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCO.0000000000000252

关键词

cancer; cellular stress response; cytosine-5 methylation; noncoding RNA; NSun proteins; stem cells

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资金

  1. Cancer Research UK (CR-UK)
  2. Worldwide Cancer Research
  3. Medical Research Council (MRC)
  4. European Research Council (ERC)
  5. EMBO
  6. Wellcome Trust
  7. MRC
  8. Cancer Research UK [15181, 16134] Funding Source: researchfish
  9. Medical Research Council [G0801904, MR/M01939X/1] Funding Source: researchfish
  10. British Skin Foundation [5010] Funding Source: researchfish
  11. Worldwide Cancer Research [15-0168] Funding Source: researchfish
  12. MRC [G0801904, MR/M01939X/1] Funding Source: UKRI

向作者/读者索取更多资源

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.

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