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MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer

MicroRNAs (miRNAs) are small, highly conserved noncoding RNAs molecules, consisting of 18–25 nucleotides that regulate gene expression by binding to complementary binding sites within the 3′untranslated region (3′UTR) of target mRNAs. MiRNAs have been involved in regulating gene expression and diver...

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Detalles Bibliográficos
Autores principales: Jiang, Lin-hong, Zhang, He-da, Tang, Jin-hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106977/
https://www.ncbi.nlm.nih.gov/pubmed/30158978
http://dx.doi.org/10.1155/2018/5167829
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author Jiang, Lin-hong
Zhang, He-da
Tang, Jin-hai
author_facet Jiang, Lin-hong
Zhang, He-da
Tang, Jin-hai
author_sort Jiang, Lin-hong
collection PubMed
description MicroRNAs (miRNAs) are small, highly conserved noncoding RNAs molecules, consisting of 18–25 nucleotides that regulate gene expression by binding to complementary binding sites within the 3′untranslated region (3′UTR) of target mRNAs. MiRNAs have been involved in regulating gene expression and diverse physiological and pathological processes. Several studies have reported that miR-30a, situated on chromosome 6q.13, is produced by an intronic transcriptional unit. Moreover, miR-30a has demonstrated its role in biological processes, including inhibiting proliferation and metastasis in many tumors, autophagy in chronic myelogenous leukemia, and regulating TGF-b1-induced epithelial-mesenchymal transition. However, based on the pathogenetic relationship between miR-30a and cancer in tumorigenesis, we believe that miR-30a may serve as tumor promising biomarker. Moreover, it would offer a therapeutic target for the treatment of cancer.
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spelling pubmed-61069772018-08-29 MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer Jiang, Lin-hong Zhang, He-da Tang, Jin-hai J Oncol Review Article MicroRNAs (miRNAs) are small, highly conserved noncoding RNAs molecules, consisting of 18–25 nucleotides that regulate gene expression by binding to complementary binding sites within the 3′untranslated region (3′UTR) of target mRNAs. MiRNAs have been involved in regulating gene expression and diverse physiological and pathological processes. Several studies have reported that miR-30a, situated on chromosome 6q.13, is produced by an intronic transcriptional unit. Moreover, miR-30a has demonstrated its role in biological processes, including inhibiting proliferation and metastasis in many tumors, autophagy in chronic myelogenous leukemia, and regulating TGF-b1-induced epithelial-mesenchymal transition. However, based on the pathogenetic relationship between miR-30a and cancer in tumorigenesis, we believe that miR-30a may serve as tumor promising biomarker. Moreover, it would offer a therapeutic target for the treatment of cancer. Hindawi 2018-08-06 /pmc/articles/PMC6106977/ /pubmed/30158978 http://dx.doi.org/10.1155/2018/5167829 Text en Copyright © 2018 Lin-hong Jiang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Jiang, Lin-hong
Zhang, He-da
Tang, Jin-hai
MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title_full MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title_fullStr MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title_full_unstemmed MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title_short MiR-30a: A Novel Biomarker and Potential Therapeutic Target for Cancer
title_sort mir-30a: a novel biomarker and potential therapeutic target for cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106977/
https://www.ncbi.nlm.nih.gov/pubmed/30158978
http://dx.doi.org/10.1155/2018/5167829
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