Cargando…

miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy

Cisplatin (DDP) resistance is one of the main causes of treatment failure in patients with colon cancer (CC). Autophagy is a key mechanism of resistance to chemotherapy. Since autophagy-related 7 (ATG7) has been reported to be involved in the regulation of autophagy and DDP resistance for lung and e...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Weiwei, Chen, Linxia, Zhu, Wenjin, Huang, Xianjin, Lin, Lin, Quan, Zhenhao, Sun, Kaiyu, Xu, Qingwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561764/
https://www.ncbi.nlm.nih.gov/pubmed/34737805
http://dx.doi.org/10.3892/etm.2021.10900
_version_ 1784593145971867648
author Wang, Weiwei
Chen, Linxia
Zhu, Wenjin
Huang, Xianjin
Lin, Lin
Quan, Zhenhao
Sun, Kaiyu
Xu, Qingwen
author_facet Wang, Weiwei
Chen, Linxia
Zhu, Wenjin
Huang, Xianjin
Lin, Lin
Quan, Zhenhao
Sun, Kaiyu
Xu, Qingwen
author_sort Wang, Weiwei
collection PubMed
description Cisplatin (DDP) resistance is one of the main causes of treatment failure in patients with colon cancer (CC). Autophagy is a key mechanism of resistance to chemotherapy. Since autophagy-related 7 (ATG7) has been reported to be involved in the regulation of autophagy and DDP resistance for lung and esophageal cancer, the present study aimed to explore the functions of microRNA (miR)-4486 in the autophagy-mediated DDP resistance of CC. The expression level of miR-4486 in HCT116, DDP-resistant HCT116 cells (HCT116/DDP), SW480 and DDP-resistant SW480 cells (SW480/DDP) was quantified by reverse transcription-quantitative PCR. Western blotting was utilized to analyze the expression of ATG7, autophagy-related proteins Beclin 1 and LC3-I/II, as well as apoptosis-related proteins Bcl-2, Bax and cleaved-caspase 3 in HCT116/DDP and SW480/DDP cells. The half maximal inhibitory concentration of DDP on all cell lines and the cell viability of HCT116/DDP and SW480/DDP cells were measured using Cell Counting Kit 8 assay. Luciferase assay was used to examine the potential targets of miR-4486 and ATG7. The effects of upregulating mimic miR-4486 expression on the apoptosis and autophagy of HCT116/DDP and SW480/DDP cells were determined by flow cytometry and electron microscopy, respectively. It was found that miR-4486 expression was significantly decreased in HCT116/DDP and SW480/DDP cells compared with that in HCT116 and SW480 cells. Overexpression of miR-4486 could increase the sensitivity of HCT116/DDP and SW480/DDP cells to DDP by reducing cell viability, promoting apoptosis and inhibiting autophagy through downregulating Beclin 1 expression and the LC3-II/LC3-I ratio. Additionally, ATG7 was identified to be a target gene of miR-4486, where ATG7 overexpression could partially reverse the effects of miR-4486 on cell viability and apoptosis by promoting the formation of autophagosomes. In conclusion, the present results demonstrated that miR-4486 could reverse DDP resistance in HCT116/DDP and SW480/DDP cells by targeting ATG7 to inhibit autophagy.
format Online
Article
Text
id pubmed-8561764
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-85617642021-11-03 miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy Wang, Weiwei Chen, Linxia Zhu, Wenjin Huang, Xianjin Lin, Lin Quan, Zhenhao Sun, Kaiyu Xu, Qingwen Exp Ther Med Articles Cisplatin (DDP) resistance is one of the main causes of treatment failure in patients with colon cancer (CC). Autophagy is a key mechanism of resistance to chemotherapy. Since autophagy-related 7 (ATG7) has been reported to be involved in the regulation of autophagy and DDP resistance for lung and esophageal cancer, the present study aimed to explore the functions of microRNA (miR)-4486 in the autophagy-mediated DDP resistance of CC. The expression level of miR-4486 in HCT116, DDP-resistant HCT116 cells (HCT116/DDP), SW480 and DDP-resistant SW480 cells (SW480/DDP) was quantified by reverse transcription-quantitative PCR. Western blotting was utilized to analyze the expression of ATG7, autophagy-related proteins Beclin 1 and LC3-I/II, as well as apoptosis-related proteins Bcl-2, Bax and cleaved-caspase 3 in HCT116/DDP and SW480/DDP cells. The half maximal inhibitory concentration of DDP on all cell lines and the cell viability of HCT116/DDP and SW480/DDP cells were measured using Cell Counting Kit 8 assay. Luciferase assay was used to examine the potential targets of miR-4486 and ATG7. The effects of upregulating mimic miR-4486 expression on the apoptosis and autophagy of HCT116/DDP and SW480/DDP cells were determined by flow cytometry and electron microscopy, respectively. It was found that miR-4486 expression was significantly decreased in HCT116/DDP and SW480/DDP cells compared with that in HCT116 and SW480 cells. Overexpression of miR-4486 could increase the sensitivity of HCT116/DDP and SW480/DDP cells to DDP by reducing cell viability, promoting apoptosis and inhibiting autophagy through downregulating Beclin 1 expression and the LC3-II/LC3-I ratio. Additionally, ATG7 was identified to be a target gene of miR-4486, where ATG7 overexpression could partially reverse the effects of miR-4486 on cell viability and apoptosis by promoting the formation of autophagosomes. In conclusion, the present results demonstrated that miR-4486 could reverse DDP resistance in HCT116/DDP and SW480/DDP cells by targeting ATG7 to inhibit autophagy. D.A. Spandidos 2021-12 2021-10-20 /pmc/articles/PMC8561764/ /pubmed/34737805 http://dx.doi.org/10.3892/etm.2021.10900 Text en Copyright: © Wang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/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
Wang, Weiwei
Chen, Linxia
Zhu, Wenjin
Huang, Xianjin
Lin, Lin
Quan, Zhenhao
Sun, Kaiyu
Xu, Qingwen
miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title_full miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title_fullStr miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title_full_unstemmed miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title_short miR-4486 reverses cisplatin-resistance of colon cancer cells via targeting ATG7 to inhibiting autophagy
title_sort mir-4486 reverses cisplatin-resistance of colon cancer cells via targeting atg7 to inhibiting autophagy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561764/
https://www.ncbi.nlm.nih.gov/pubmed/34737805
http://dx.doi.org/10.3892/etm.2021.10900
work_keys_str_mv AT wangweiwei mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT chenlinxia mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT zhuwenjin mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT huangxianjin mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT linlin mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT quanzhenhao mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT sunkaiyu mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy
AT xuqingwen mir4486reversescisplatinresistanceofcoloncancercellsviatargetingatg7toinhibitingautophagy