miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2

Gastric cancer(GC) is the fourth most common cancer in the world. This work was designed to explore the biological effects of miR-148-3p on GC. Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was utilized to analyze the mRNA expression of miR-148-3p in GC cell lines. The mimic...

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Autores principales: Hongyan Zhang, Feng Liang, Fei Wang, Qianru Xu, Yuxuan Qiu, Xin Lu, Lin Jiang, Kaiyu Jian
Formato: article
Lenguaje:EN
Publicado: Taylor & Francis Group 2021
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Acceso en línea:https://doaj.org/article/28bc2d0d32b3485ea0aba40533ff38f0
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spelling oai:doaj.org-article:28bc2d0d32b3485ea0aba40533ff38f02021-11-17T14:21:59ZmiR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl22165-59792165-598710.1080/21655979.2021.2005742https://doaj.org/article/28bc2d0d32b3485ea0aba40533ff38f02021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.2005742https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Gastric cancer(GC) is the fourth most common cancer in the world. This work was designed to explore the biological effects of miR-148-3p on GC. Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was utilized to analyze the mRNA expression of miR-148-3p in GC cell lines. The mimics and inhibitors of miR-148-3p, was carefully transfected into GC cells to up-regulate or down-regulate miR-148-3p expression. Observe the effect on miR-148-3p expression change to GC cell proliferation, colony formation, tumorigenesis, chemotherapy sensitivity, trans-well migration and invasion. Use online database tool to predict the miR-148-3p promising targets, and be verified via RT-qPCR, Western blot and luciferase report. We found that miR-148-3p expression level in GC cells was markedly down-regulated (P <0.05), as compared with human normal gastric mucosal cells GES-1. Otherwise, miR-148-3p overexpression could effectively inhibit the cell proliferation, cell cycle progress, colony formation, anti-apoptosis, anti-migration and anti-invasion in gastric cancer cells, whereas miR-148-3p inhibition exhibited the opposite phenomenon (P<0.05). Further research revealed that Bcl2 set as a direct downstream target of miR-148-3p. Our study firstly confirmed that, miR-148-3p might play a crucial role in tumorigenesis, as well as development of gastric cancer by targeting Bcl2, and could become a promising target for gastric cancer treatment.Hongyan ZhangFeng LiangFei WangQianru XuYuxuan QiuXin LuLin JiangKaiyu JianTaylor & Francis Grouparticlemir-148-3pbcl2cell proliferation and invasiongastric cancerchemotherapy resistanceBiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic mir-148-3p
bcl2
cell proliferation and invasion
gastric cancer
chemotherapy resistance
Biotechnology
TP248.13-248.65
spellingShingle mir-148-3p
bcl2
cell proliferation and invasion
gastric cancer
chemotherapy resistance
Biotechnology
TP248.13-248.65
Hongyan Zhang
Feng Liang
Fei Wang
Qianru Xu
Yuxuan Qiu
Xin Lu
Lin Jiang
Kaiyu Jian
miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
description Gastric cancer(GC) is the fourth most common cancer in the world. This work was designed to explore the biological effects of miR-148-3p on GC. Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was utilized to analyze the mRNA expression of miR-148-3p in GC cell lines. The mimics and inhibitors of miR-148-3p, was carefully transfected into GC cells to up-regulate or down-regulate miR-148-3p expression. Observe the effect on miR-148-3p expression change to GC cell proliferation, colony formation, tumorigenesis, chemotherapy sensitivity, trans-well migration and invasion. Use online database tool to predict the miR-148-3p promising targets, and be verified via RT-qPCR, Western blot and luciferase report. We found that miR-148-3p expression level in GC cells was markedly down-regulated (P <0.05), as compared with human normal gastric mucosal cells GES-1. Otherwise, miR-148-3p overexpression could effectively inhibit the cell proliferation, cell cycle progress, colony formation, anti-apoptosis, anti-migration and anti-invasion in gastric cancer cells, whereas miR-148-3p inhibition exhibited the opposite phenomenon (P<0.05). Further research revealed that Bcl2 set as a direct downstream target of miR-148-3p. Our study firstly confirmed that, miR-148-3p might play a crucial role in tumorigenesis, as well as development of gastric cancer by targeting Bcl2, and could become a promising target for gastric cancer treatment.
format article
author Hongyan Zhang
Feng Liang
Fei Wang
Qianru Xu
Yuxuan Qiu
Xin Lu
Lin Jiang
Kaiyu Jian
author_facet Hongyan Zhang
Feng Liang
Fei Wang
Qianru Xu
Yuxuan Qiu
Xin Lu
Lin Jiang
Kaiyu Jian
author_sort Hongyan Zhang
title miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
title_short miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
title_full miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
title_fullStr miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
title_full_unstemmed miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2
title_sort mir-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting bcl2
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/28bc2d0d32b3485ea0aba40533ff38f0
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AT fengliang mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
AT feiwang mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
AT qianruxu mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
AT yuxuanqiu mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
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AT linjiang mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
AT kaiyujian mir1483pinhibitsgastriccancercellmalignantphenotypesandchemotherapyresistancebytargetingbcl2
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