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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...

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Detalles Bibliográficos
Autores principales: Imani, Saber, Wu, Ray-Chang, Fu, Junjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
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.
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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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