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Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells

Lung cancer is the most prevalent type of cancer worldwide and is the leading cause of cancer-associated cases of mortality in the USA and China. Non-small cell lung cancer (NSCLC) accounts for 80–85% of lung cancer cases. microRNAs (miRs) serve multiple roles in the pathogenesis of lung cancer. The...

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Autores principales: Huang, Yan, Bao, Ting, Li, Zhenzhen, Ji, Guiyi, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377081/
https://www.ncbi.nlm.nih.gov/pubmed/32724366
http://dx.doi.org/10.3892/ol.2020.11649
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author Huang, Yan
Bao, Ting
Li, Zhenzhen
Ji, Guiyi
Zhang, Li
author_facet Huang, Yan
Bao, Ting
Li, Zhenzhen
Ji, Guiyi
Zhang, Li
author_sort Huang, Yan
collection PubMed
description Lung cancer is the most prevalent type of cancer worldwide and is the leading cause of cancer-associated cases of mortality in the USA and China. Non-small cell lung cancer (NSCLC) accounts for 80–85% of lung cancer cases. microRNAs (miRs) serve multiple roles in the pathogenesis of lung cancer. The current study investigated the lower level of miR-200a in tumor tissues compared with healthy tissue. Overexpression of miR-200a inhibited NSCLC cell proliferation and promoted apoptosis. miR-200a was identified to target Rhophilin Rho GTPase binding protein 2 (RHPN2) and higher levels of RHPN2 were observed in tumor tissues compared with adjacent normal tissues. The current study proposes that miR-200a exhibits a tumor suppressive role in NSCLC and suggests that miR-200a could target RHPN2.
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spelling pubmed-73770812020-07-27 Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells Huang, Yan Bao, Ting Li, Zhenzhen Ji, Guiyi Zhang, Li Oncol Lett Articles Lung cancer is the most prevalent type of cancer worldwide and is the leading cause of cancer-associated cases of mortality in the USA and China. Non-small cell lung cancer (NSCLC) accounts for 80–85% of lung cancer cases. microRNAs (miRs) serve multiple roles in the pathogenesis of lung cancer. The current study investigated the lower level of miR-200a in tumor tissues compared with healthy tissue. Overexpression of miR-200a inhibited NSCLC cell proliferation and promoted apoptosis. miR-200a was identified to target Rhophilin Rho GTPase binding protein 2 (RHPN2) and higher levels of RHPN2 were observed in tumor tissues compared with adjacent normal tissues. The current study proposes that miR-200a exhibits a tumor suppressive role in NSCLC and suggests that miR-200a could target RHPN2. D.A. Spandidos 2020-08 2020-05-20 /pmc/articles/PMC7377081/ /pubmed/32724366 http://dx.doi.org/10.3892/ol.2020.11649 Text en Copyright: © Huang 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 Articles
Huang, Yan
Bao, Ting
Li, Zhenzhen
Ji, Guiyi
Zhang, Li
Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title_full Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title_fullStr Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title_full_unstemmed Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title_short Function of miR-200a in proliferation and apoptosis of non-small cell lung cancer cells
title_sort function of mir-200a in proliferation and apoptosis of non-small cell lung cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377081/
https://www.ncbi.nlm.nih.gov/pubmed/32724366
http://dx.doi.org/10.3892/ol.2020.11649
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