LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p
Zhe Song,1 Nan Jia,1 Wei Li,1 Xiao-Yu Zhang2 1Second Department of General Surgery, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland China; 2Department of Thyroid and Breast III, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland ChinaCorrespondence: Xiao-Yu ZhangDepartment o...
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doaj-6f6f218f116f4b91a817083fdcc61b702020-11-25T03:36:09ZengDove Medical PressOncoTargets and Therapy1178-69302020-10-01Volume 13108771088758513LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5pSong ZJia NLi WZhang XYZhe Song,1 Nan Jia,1 Wei Li,1 Xiao-Yu Zhang2 1Second Department of General Surgery, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland China; 2Department of Thyroid and Breast III, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland ChinaCorrespondence: Xiao-Yu ZhangDepartment of Thyroid and Breast III, Cangzhou Central Hospital, Cangzhou, Hebei Province, People’s Republic of ChinaEmail zhangxiaoyu9321@163.comBackground: Chemotherapy resistance has long been recognized as a major obstacle to cancer treatment. Therefore, elucidating the underlying mechanisms of chemotherapy resistance is conducive to developing new strategies to improve patients’ response to chemotherapy drugs.Materials and Methods: Real-time quantitative PCR (QPCR) was applied to measure the expression levels of lncRNAs. LINC01572 was down-regulated or up-regulated in GC cells transfected with either LINC01572 shRNA or overexpression vectors. In vitro and in vivo experiments were conducted to investigate the role of LINC01572 in autophagy-related chemotherapy resistance.Results: Compared with the parental cells, drug-resistant GC cells had a higher level of LINC01572. Silencing of LINC01572 inhibited chemotherapy-induced autophagy, while its knockout sensitized GC cells against chemotherapy drugs. As a competitive endogenous RNA of miR-497-5p, LINC01572 weakened the inhibitory effect of miR-497-5p on ATG14, leading to chemically induced autophagy and chemotherapy resistance in GC cells.Conclusion: A new mechanism of GC autophagy-related chemotherapy resistance regulated by lncRNA was explored in this study, providing a new perspective for understanding chemotherapy resistance.Keywords: LINC01572, miR-497-5p, gastric cancer, drug resistancehttps://www.dovepress.com/linc01572-regulates-cisplatin-resistance-in-gastric-cancer-cells-by-me-peer-reviewed-article-OTTlinc01572mir-497-5pgastric cancerdrug resistance |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Song Z Jia N Li W Zhang XY |
spellingShingle |
Song Z Jia N Li W Zhang XY LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p OncoTargets and Therapy linc01572 mir-497-5p gastric cancer drug resistance |
author_facet |
Song Z Jia N Li W Zhang XY |
author_sort |
Song Z |
title |
LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p |
title_short |
LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p |
title_full |
LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p |
title_fullStr |
LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p |
title_full_unstemmed |
LINC01572 Regulates Cisplatin Resistance in Gastric Cancer Cells by Mediating miR-497-5p |
title_sort |
linc01572 regulates cisplatin resistance in gastric cancer cells by mediating mir-497-5p |
publisher |
Dove Medical Press |
series |
OncoTargets and Therapy |
issn |
1178-6930 |
publishDate |
2020-10-01 |
description |
Zhe Song,1 Nan Jia,1 Wei Li,1 Xiao-Yu Zhang2 1Second Department of General Surgery, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland China; 2Department of Thyroid and Breast III, Cangzhou Central Hospital, Cangzhou, Hebei Province, Mainland ChinaCorrespondence: Xiao-Yu ZhangDepartment of Thyroid and Breast III, Cangzhou Central Hospital, Cangzhou, Hebei Province, People’s Republic of ChinaEmail zhangxiaoyu9321@163.comBackground: Chemotherapy resistance has long been recognized as a major obstacle to cancer treatment. Therefore, elucidating the underlying mechanisms of chemotherapy resistance is conducive to developing new strategies to improve patients’ response to chemotherapy drugs.Materials and Methods: Real-time quantitative PCR (QPCR) was applied to measure the expression levels of lncRNAs. LINC01572 was down-regulated or up-regulated in GC cells transfected with either LINC01572 shRNA or overexpression vectors. In vitro and in vivo experiments were conducted to investigate the role of LINC01572 in autophagy-related chemotherapy resistance.Results: Compared with the parental cells, drug-resistant GC cells had a higher level of LINC01572. Silencing of LINC01572 inhibited chemotherapy-induced autophagy, while its knockout sensitized GC cells against chemotherapy drugs. As a competitive endogenous RNA of miR-497-5p, LINC01572 weakened the inhibitory effect of miR-497-5p on ATG14, leading to chemically induced autophagy and chemotherapy resistance in GC cells.Conclusion: A new mechanism of GC autophagy-related chemotherapy resistance regulated by lncRNA was explored in this study, providing a new perspective for understanding chemotherapy resistance.Keywords: LINC01572, miR-497-5p, gastric cancer, drug resistance |
topic |
linc01572 mir-497-5p gastric cancer drug resistance |
url |
https://www.dovepress.com/linc01572-regulates-cisplatin-resistance-in-gastric-cancer-cells-by-me-peer-reviewed-article-OTT |
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