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The Emerging Roles of miR-125b in Cancers

MicroRNAs (miRNAs) are endogenous, noncoding, single-stranded RNA molecules of 22 nucleotides in length. MiRNAs have both tumor-suppressive properties and oncogenic properties that can control critical processes in tumors. Mature miR-125b originates from miR-125b-1 and miR-125b-2 and leads to the de...

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Detalles Bibliográficos
Autores principales: Wang, Ying, Zeng, Guilin, Jiang, Yicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024862/
https://www.ncbi.nlm.nih.gov/pubmed/32104088
http://dx.doi.org/10.2147/CMAR.S232388
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author Wang, Ying
Zeng, Guilin
Jiang, Yicheng
author_facet Wang, Ying
Zeng, Guilin
Jiang, Yicheng
author_sort Wang, Ying
collection PubMed
description MicroRNAs (miRNAs) are endogenous, noncoding, single-stranded RNA molecules of 22 nucleotides in length. MiRNAs have both tumor-suppressive properties and oncogenic properties that can control critical processes in tumors. Mature miR-125b originates from miR-125b-1 and miR-125b-2 and leads to the degradation of target mRNAs or the inhibition of translation through binding to the 3′ untranslated regions (3′-UTR) of target mRNAs. Importantly, miR-125b is involved in regulating NF-κB, p53, PI3K/Akt/mTOR, ErbB2, Wnt, and another signaling pathways, thereby controlling cell proliferation, differentiation, metabolism, apoptosis, drug resistance and tumor immunity. This review aims to summarize the recent literature on the role of miR-125b in the regulation of tumorigenesis and to explore its potential clinical application in the diagnosis, prognosis and clinical treatment of tumors.
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spelling pubmed-70248622020-02-26 The Emerging Roles of miR-125b in Cancers Wang, Ying Zeng, Guilin Jiang, Yicheng Cancer Manag Res Review MicroRNAs (miRNAs) are endogenous, noncoding, single-stranded RNA molecules of 22 nucleotides in length. MiRNAs have both tumor-suppressive properties and oncogenic properties that can control critical processes in tumors. Mature miR-125b originates from miR-125b-1 and miR-125b-2 and leads to the degradation of target mRNAs or the inhibition of translation through binding to the 3′ untranslated regions (3′-UTR) of target mRNAs. Importantly, miR-125b is involved in regulating NF-κB, p53, PI3K/Akt/mTOR, ErbB2, Wnt, and another signaling pathways, thereby controlling cell proliferation, differentiation, metabolism, apoptosis, drug resistance and tumor immunity. This review aims to summarize the recent literature on the role of miR-125b in the regulation of tumorigenesis and to explore its potential clinical application in the diagnosis, prognosis and clinical treatment of tumors. Dove 2020-02-12 /pmc/articles/PMC7024862/ /pubmed/32104088 http://dx.doi.org/10.2147/CMAR.S232388 Text en © 2020 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Wang, Ying
Zeng, Guilin
Jiang, Yicheng
The Emerging Roles of miR-125b in Cancers
title The Emerging Roles of miR-125b in Cancers
title_full The Emerging Roles of miR-125b in Cancers
title_fullStr The Emerging Roles of miR-125b in Cancers
title_full_unstemmed The Emerging Roles of miR-125b in Cancers
title_short The Emerging Roles of miR-125b in Cancers
title_sort emerging roles of mir-125b in cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024862/
https://www.ncbi.nlm.nih.gov/pubmed/32104088
http://dx.doi.org/10.2147/CMAR.S232388
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