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Role of microRNA-33a in malignant cells

Cancer causes most of the mortality and morbidity worldwide, with a significant increase in incidence during recent years. MicroRNAs (miRNAs/miRs) are non-coding small RNAs capable of regulating gene expression. They regulate crucial cellular processes, including proliferation, differentiation, meta...

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Autores principales: Gao, Chang, Wei, Jiaen, Tang, Tingting, Huang, Zunnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399786/
https://www.ncbi.nlm.nih.gov/pubmed/32782572
http://dx.doi.org/10.3892/ol.2020.11835
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author Gao, Chang
Wei, Jiaen
Tang, Tingting
Huang, Zunnan
author_facet Gao, Chang
Wei, Jiaen
Tang, Tingting
Huang, Zunnan
author_sort Gao, Chang
collection PubMed
description Cancer causes most of the mortality and morbidity worldwide, with a significant increase in incidence during recent years. MicroRNAs (miRNAs/miRs) are non-coding small RNAs capable of regulating gene expression. They regulate crucial cellular processes, including proliferation, differentiation, metastasis and apoptosis. Therefore, abnormal miRNA expression is associated with multiple diseases, including cancer. There are two types of cancer-associated miRNAs, oncogenic and tumor suppressor miRNAs, depending on their roles and expression patterns in cancer. Accordingly, miRNAs are considered to be targets for cancer prevention and treatment. miR-33a controls cellular cholesterol uptake and synthesis, which are both closely associated with carcinogenesis. The present review thoroughly describes the roles of miR-33a in more than a dozen types of cancer and the underlying mechanisms. Accordingly, the present review may serve as a guide for researchers studying the involvement of miR-33a in diverse cancer settings.
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spelling pubmed-73997862020-08-10 Role of microRNA-33a in malignant cells Gao, Chang Wei, Jiaen Tang, Tingting Huang, Zunnan Oncol Lett Review Cancer causes most of the mortality and morbidity worldwide, with a significant increase in incidence during recent years. MicroRNAs (miRNAs/miRs) are non-coding small RNAs capable of regulating gene expression. They regulate crucial cellular processes, including proliferation, differentiation, metastasis and apoptosis. Therefore, abnormal miRNA expression is associated with multiple diseases, including cancer. There are two types of cancer-associated miRNAs, oncogenic and tumor suppressor miRNAs, depending on their roles and expression patterns in cancer. Accordingly, miRNAs are considered to be targets for cancer prevention and treatment. miR-33a controls cellular cholesterol uptake and synthesis, which are both closely associated with carcinogenesis. The present review thoroughly describes the roles of miR-33a in more than a dozen types of cancer and the underlying mechanisms. Accordingly, the present review may serve as a guide for researchers studying the involvement of miR-33a in diverse cancer settings. D.A. Spandidos 2020-09 2020-07-09 /pmc/articles/PMC7399786/ /pubmed/32782572 http://dx.doi.org/10.3892/ol.2020.11835 Text en Copyright: © Gao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Gao, Chang
Wei, Jiaen
Tang, Tingting
Huang, Zunnan
Role of microRNA-33a in malignant cells
title Role of microRNA-33a in malignant cells
title_full Role of microRNA-33a in malignant cells
title_fullStr Role of microRNA-33a in malignant cells
title_full_unstemmed Role of microRNA-33a in malignant cells
title_short Role of microRNA-33a in malignant cells
title_sort role of microrna-33a in malignant cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399786/
https://www.ncbi.nlm.nih.gov/pubmed/32782572
http://dx.doi.org/10.3892/ol.2020.11835
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