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Systematic characterization of non‐coding RNAs in triple‐negative breast cancer

Triple‐negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer with negativity for oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor (HER2). Non‐coding RNAs (ncRNAs) make up most of the transcriptome and are widely present in...

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Autores principales: Mei, Jie, Hao, Leiyu, Wang, Huiyu, Xu, Rui, Liu, Yan, Zhu, Yichao, Liu, Chaoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260065/
https://www.ncbi.nlm.nih.gov/pubmed/32249490
http://dx.doi.org/10.1111/cpr.12801
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author Mei, Jie
Hao, Leiyu
Wang, Huiyu
Xu, Rui
Liu, Yan
Zhu, Yichao
Liu, Chaoying
author_facet Mei, Jie
Hao, Leiyu
Wang, Huiyu
Xu, Rui
Liu, Yan
Zhu, Yichao
Liu, Chaoying
author_sort Mei, Jie
collection PubMed
description Triple‐negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer with negativity for oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor (HER2). Non‐coding RNAs (ncRNAs) make up most of the transcriptome and are widely present in eukaryotic cells. In recent years, emerging evidence suggests that ncRNAs, mainly microRNAs (miRNAs), long ncRNAs (lncRNAs) and circular RNAs (circRNAs), play prominent roles in the tumorigenesis and development of TNBC, but the functions of most ncRNAs have not been fully described. In this review, we systematically elucidate the general characteristics and biogenesis of miRNAs, lncRNAs and circRNAs, discuss the emerging functions of these ncRNAs in TNBC and present future perspectives in clinical practice.
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spelling pubmed-72600652020-06-01 Systematic characterization of non‐coding RNAs in triple‐negative breast cancer Mei, Jie Hao, Leiyu Wang, Huiyu Xu, Rui Liu, Yan Zhu, Yichao Liu, Chaoying Cell Prolif Reviews Triple‐negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer with negativity for oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor (HER2). Non‐coding RNAs (ncRNAs) make up most of the transcriptome and are widely present in eukaryotic cells. In recent years, emerging evidence suggests that ncRNAs, mainly microRNAs (miRNAs), long ncRNAs (lncRNAs) and circular RNAs (circRNAs), play prominent roles in the tumorigenesis and development of TNBC, but the functions of most ncRNAs have not been fully described. In this review, we systematically elucidate the general characteristics and biogenesis of miRNAs, lncRNAs and circRNAs, discuss the emerging functions of these ncRNAs in TNBC and present future perspectives in clinical practice. John Wiley and Sons Inc. 2020-04-06 /pmc/articles/PMC7260065/ /pubmed/32249490 http://dx.doi.org/10.1111/cpr.12801 Text en © 2020 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Mei, Jie
Hao, Leiyu
Wang, Huiyu
Xu, Rui
Liu, Yan
Zhu, Yichao
Liu, Chaoying
Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title_full Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title_fullStr Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title_full_unstemmed Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title_short Systematic characterization of non‐coding RNAs in triple‐negative breast cancer
title_sort systematic characterization of non‐coding rnas in triple‐negative breast cancer
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260065/
https://www.ncbi.nlm.nih.gov/pubmed/32249490
http://dx.doi.org/10.1111/cpr.12801
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