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Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer
Breast cancer is believed to be driven by epigenetic regulation of genes implicated in cell proliferation, survival, and differentiation. Recently, aberrant N(6)-methyladenosine (m(6)A) decorations turned up as crucial epigenetic regulator for malignant breast cancer, which may serve as new targets...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138681/ https://www.ncbi.nlm.nih.gov/pubmed/34000587 http://dx.doi.org/10.1016/j.neo.2021.04.002 |
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author | Fang, Runping Ye, Lihong Shi, Hui |
author_facet | Fang, Runping Ye, Lihong Shi, Hui |
author_sort | Fang, Runping |
collection | PubMed |
description | Breast cancer is believed to be driven by epigenetic regulation of genes implicated in cell proliferation, survival, and differentiation. Recently, aberrant N(6)-methyladenosine (m(6)A) decorations turned up as crucial epigenetic regulator for malignant breast cancer, which may serve as new targets for breast cancer treatment. Here we briefly outline the functions of m(6)A and its regulatory proteins, including m(6)A “writers,” “readers,” and “erasers” on RNA life fate, recapitulate the latest breakthroughs in understanding m(6)A modification and its regulatory proteins, and the underlying molecular mechanisms that contribute to the carcinogenesis and the progression of breast cancer, so as to provide potential epigenetic targets for diagnosis, treatment and prognosis in breast cancer. |
format | Online Article Text |
id | pubmed-8138681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81386812021-05-24 Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer Fang, Runping Ye, Lihong Shi, Hui Neoplasia Review Article Breast cancer is believed to be driven by epigenetic regulation of genes implicated in cell proliferation, survival, and differentiation. Recently, aberrant N(6)-methyladenosine (m(6)A) decorations turned up as crucial epigenetic regulator for malignant breast cancer, which may serve as new targets for breast cancer treatment. Here we briefly outline the functions of m(6)A and its regulatory proteins, including m(6)A “writers,” “readers,” and “erasers” on RNA life fate, recapitulate the latest breakthroughs in understanding m(6)A modification and its regulatory proteins, and the underlying molecular mechanisms that contribute to the carcinogenesis and the progression of breast cancer, so as to provide potential epigenetic targets for diagnosis, treatment and prognosis in breast cancer. Neoplasia Press 2021-05-14 /pmc/articles/PMC8138681/ /pubmed/34000587 http://dx.doi.org/10.1016/j.neo.2021.04.002 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Fang, Runping Ye, Lihong Shi, Hui Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title | Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title_full | Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title_fullStr | Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title_full_unstemmed | Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title_short | Understanding the roles of N(6)-methyladenosine writers, readers and erasers in breast cancer |
title_sort | understanding the roles of n(6)-methyladenosine writers, readers and erasers in breast cancer |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138681/ https://www.ncbi.nlm.nih.gov/pubmed/34000587 http://dx.doi.org/10.1016/j.neo.2021.04.002 |
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