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MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities

MicroRNAs (miRNAs) are endogenous non-coding small RNAs that downregulate target gene expression by imperfect base-pairing with the 3′ untranslated regions (3′UTRs) of target gene mRNAs. MiRNAs play important roles in regulating cancer cell proliferation, stemness maintenance, tumorigenesis, cancer...

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Detalles Bibliográficos
Autores principales: Xiao, Yajuan, Humphries, Brock, Yang, Chengfeng, Wang, Zhishan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958506/
https://www.ncbi.nlm.nih.gov/pubmed/31752366
http://dx.doi.org/10.3390/ncrna5040053
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author Xiao, Yajuan
Humphries, Brock
Yang, Chengfeng
Wang, Zhishan
author_facet Xiao, Yajuan
Humphries, Brock
Yang, Chengfeng
Wang, Zhishan
author_sort Xiao, Yajuan
collection PubMed
description MicroRNAs (miRNAs) are endogenous non-coding small RNAs that downregulate target gene expression by imperfect base-pairing with the 3′ untranslated regions (3′UTRs) of target gene mRNAs. MiRNAs play important roles in regulating cancer cell proliferation, stemness maintenance, tumorigenesis, cancer metastasis, and cancer therapeutic resistance. While studies have shown that dysregulation of miRNA-205-5p (miR-205) expression is controversial in different types of human cancers, it is generally observed that miR-205-5p expression level is downregulated in breast cancer and that miR-205-5p exhibits a tumor suppressive function in breast cancer. This review focuses on the role of miR-205-5p dysregulation in different subtypes of breast cancer, with discussions on the effects of miR-205-5p on breast cancer cell proliferation, epithelial–mesenchymal transition (EMT), metastasis, stemness and therapy-resistance, as well as genetic and epigenetic mechanisms that regulate miR-205-5p expression in breast cancer. In addition, the potential diagnostic and therapeutic value of miR-205-5p in breast cancer is also discussed. A comprehensive list of validated miR-205-5p direct targets is presented. It is concluded that miR-205-5p is an important tumor suppressive miRNA capable of inhibiting the growth and metastasis of human breast cancer, especially triple negative breast cancer. MiR-205-5p might be both a potential diagnostic biomarker and a therapeutic target for metastatic breast cancer.
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spelling pubmed-69585062020-01-23 MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities Xiao, Yajuan Humphries, Brock Yang, Chengfeng Wang, Zhishan Noncoding RNA Review MicroRNAs (miRNAs) are endogenous non-coding small RNAs that downregulate target gene expression by imperfect base-pairing with the 3′ untranslated regions (3′UTRs) of target gene mRNAs. MiRNAs play important roles in regulating cancer cell proliferation, stemness maintenance, tumorigenesis, cancer metastasis, and cancer therapeutic resistance. While studies have shown that dysregulation of miRNA-205-5p (miR-205) expression is controversial in different types of human cancers, it is generally observed that miR-205-5p expression level is downregulated in breast cancer and that miR-205-5p exhibits a tumor suppressive function in breast cancer. This review focuses on the role of miR-205-5p dysregulation in different subtypes of breast cancer, with discussions on the effects of miR-205-5p on breast cancer cell proliferation, epithelial–mesenchymal transition (EMT), metastasis, stemness and therapy-resistance, as well as genetic and epigenetic mechanisms that regulate miR-205-5p expression in breast cancer. In addition, the potential diagnostic and therapeutic value of miR-205-5p in breast cancer is also discussed. A comprehensive list of validated miR-205-5p direct targets is presented. It is concluded that miR-205-5p is an important tumor suppressive miRNA capable of inhibiting the growth and metastasis of human breast cancer, especially triple negative breast cancer. MiR-205-5p might be both a potential diagnostic biomarker and a therapeutic target for metastatic breast cancer. MDPI 2019-11-19 /pmc/articles/PMC6958506/ /pubmed/31752366 http://dx.doi.org/10.3390/ncrna5040053 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Xiao, Yajuan
Humphries, Brock
Yang, Chengfeng
Wang, Zhishan
MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title_full MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title_fullStr MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title_full_unstemmed MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title_short MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
title_sort mir-205 dysregulations in breast cancer: the complexity and opportunities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958506/
https://www.ncbi.nlm.nih.gov/pubmed/31752366
http://dx.doi.org/10.3390/ncrna5040053
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