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miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells

Elucidation of the mechanisms underlying multidrug resistance (MDR) is required to ensure the efficacy of chemotherapy against gastric cancer (GC). To investigate this issue, here we identified that microRNA‐765 (miRNA‐765) is up‐regulated both in MDR GC cell lines and in specimens from patients who...

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Autores principales: Lin, Wan, Miao, Yu, Meng, Xiangkun, Huang, Ying, Zhao, Wanli, Ruan, Jigang
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/PMC7262883/
https://www.ncbi.nlm.nih.gov/pubmed/32166887
http://dx.doi.org/10.1002/2211-5463.12838
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author Lin, Wan
Miao, Yu
Meng, Xiangkun
Huang, Ying
Zhao, Wanli
Ruan, Jigang
author_facet Lin, Wan
Miao, Yu
Meng, Xiangkun
Huang, Ying
Zhao, Wanli
Ruan, Jigang
author_sort Lin, Wan
collection PubMed
description Elucidation of the mechanisms underlying multidrug resistance (MDR) is required to ensure the efficacy of chemotherapy against gastric cancer (GC). To investigate this issue, here we identified that microRNA‐765 (miRNA‐765) is up‐regulated both in MDR GC cell lines and in specimens from patients who are not responding to chemotherapy. In addition, down‐regulation of miRNA‐765 increased the sensitivity of GC cells to anticancer drugs, whereas its overexpression had the opposite effect. Moreover, miRNA‐765 suppressed drug‐induced apoptosis and positively regulated the expression of MDR‐related genes. Finally, we showed that the basic leucine zipper ATF‐like transcription factor 2, a tumor suppressor gene, is the functional target of miRNA‐765. In summary, these results suggest that miRNA‐765 may promote MDR via basic leucine zipper ATF‐like transcription factor 2 in GC cells.
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spelling pubmed-72628832020-06-01 miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells Lin, Wan Miao, Yu Meng, Xiangkun Huang, Ying Zhao, Wanli Ruan, Jigang FEBS Open Bio Research Articles Elucidation of the mechanisms underlying multidrug resistance (MDR) is required to ensure the efficacy of chemotherapy against gastric cancer (GC). To investigate this issue, here we identified that microRNA‐765 (miRNA‐765) is up‐regulated both in MDR GC cell lines and in specimens from patients who are not responding to chemotherapy. In addition, down‐regulation of miRNA‐765 increased the sensitivity of GC cells to anticancer drugs, whereas its overexpression had the opposite effect. Moreover, miRNA‐765 suppressed drug‐induced apoptosis and positively regulated the expression of MDR‐related genes. Finally, we showed that the basic leucine zipper ATF‐like transcription factor 2, a tumor suppressor gene, is the functional target of miRNA‐765. In summary, these results suggest that miRNA‐765 may promote MDR via basic leucine zipper ATF‐like transcription factor 2 in GC cells. John Wiley and Sons Inc. 2020-04-18 /pmc/articles/PMC7262883/ /pubmed/32166887 http://dx.doi.org/10.1002/2211-5463.12838 Text en © 2020 The Authors. Published by FEBS Press and 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 Research Articles
Lin, Wan
Miao, Yu
Meng, Xiangkun
Huang, Ying
Zhao, Wanli
Ruan, Jigang
miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title_full miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title_fullStr miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title_full_unstemmed miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title_short miRNA‐765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells
title_sort mirna‐765 mediates multidrug resistance via targeting batf2 in gastric cancer cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262883/
https://www.ncbi.nlm.nih.gov/pubmed/32166887
http://dx.doi.org/10.1002/2211-5463.12838
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