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MicroRNA-34 family in breast cancer: from research to therapeutic potential
MicroRNA (miRNA)-34 family (miR-34s), including miR-34a/b/c, is the most well studied non-coding RNAs that regulate gene expression post-transcriptionally. The miR-34s mediates the tumor suppressor function of p53 in the pathogenesis of breast cancer by targeting different oncogenes. This review foc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216011/ https://www.ncbi.nlm.nih.gov/pubmed/30405848 http://dx.doi.org/10.7150/jca.25576 |
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author | Imani, Saber Wu, Ray-Chang Fu, Junjiang |
author_facet | Imani, Saber Wu, Ray-Chang Fu, Junjiang |
author_sort | Imani, Saber |
collection | PubMed |
description | MicroRNA (miRNA)-34 family (miR-34s), including miR-34a/b/c, is the most well studied non-coding RNAs that regulate gene expression post-transcriptionally. The miR-34s mediates the tumor suppressor function of p53 in the pathogenesis of breast cancer by targeting different oncogenes. This review focuses on the anti-oncogenic regulation of the miR-34s, emphasizing the major signaling pathways that are involved in the modulation of miR-34s in breast cancer. Moreover, it highlights how epigenetic modification by the p53/miR-34s axis regulates the proliferation, invasiveness, chemoresistance, and sternness of breast cancer. A better understanding of the molecular mechanisms of miR-34s will open new opportunities for the development of novel therapeutic strategies and define a new approach in identifying potential biomarkers for early diagnosis of breast cancer. |
format | Online Article Text |
id | pubmed-6216011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-62160112018-11-07 MicroRNA-34 family in breast cancer: from research to therapeutic potential Imani, Saber Wu, Ray-Chang Fu, Junjiang J Cancer Review MicroRNA (miRNA)-34 family (miR-34s), including miR-34a/b/c, is the most well studied non-coding RNAs that regulate gene expression post-transcriptionally. The miR-34s mediates the tumor suppressor function of p53 in the pathogenesis of breast cancer by targeting different oncogenes. This review focuses on the anti-oncogenic regulation of the miR-34s, emphasizing the major signaling pathways that are involved in the modulation of miR-34s in breast cancer. Moreover, it highlights how epigenetic modification by the p53/miR-34s axis regulates the proliferation, invasiveness, chemoresistance, and sternness of breast cancer. A better understanding of the molecular mechanisms of miR-34s will open new opportunities for the development of novel therapeutic strategies and define a new approach in identifying potential biomarkers for early diagnosis of breast cancer. Ivyspring International Publisher 2018-09-28 /pmc/articles/PMC6216011/ /pubmed/30405848 http://dx.doi.org/10.7150/jca.25576 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Imani, Saber Wu, Ray-Chang Fu, Junjiang MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title | MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title_full | MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title_fullStr | MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title_full_unstemmed | MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title_short | MicroRNA-34 family in breast cancer: from research to therapeutic potential |
title_sort | microrna-34 family in breast cancer: from research to therapeutic potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216011/ https://www.ncbi.nlm.nih.gov/pubmed/30405848 http://dx.doi.org/10.7150/jca.25576 |
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