MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)

MicroRNA (miR)-140-3p has been proved to repress lung adenocarcinoma (LUAD), and our study aims to further evaluate the mechanism. Bioinformatic analyses were performed. The viability, proliferation, migration, invasion and angiogenesis of transfected LUAD cells were all determined via Cell Counting...

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Autores principales: Shanzhi Wan, Zhimin Liu, Yang Chen, Zhitao Mai, Mingming Jiang, Qingguo Di, Baohua Sun
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Publicado: Taylor & Francis Group 2021
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spelling oai:doaj.org-article:339c2728e55e404388911ee22047dd0e2021-11-26T11:19:50ZMicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)2165-59792165-598710.1080/21655979.2021.2009422https://doaj.org/article/339c2728e55e404388911ee22047dd0e2021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.2009422https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987MicroRNA (miR)-140-3p has been proved to repress lung adenocarcinoma (LUAD), and our study aims to further evaluate the mechanism. Bioinformatic analyses were performed. The viability, proliferation, migration, invasion and angiogenesis of transfected LUAD cells were all determined via Cell Counting Kit-8, colony formation, Scratch, Transwell, and tube formation assays. The targeting relationship between miR-140-3p and Thymidylate Synthetase (TYMS) was confirmed by dual-luciferase reporter (DLR) assay. Relative expressions of miR-140-3p, TYMS, metastasis- (E-Cadherin, N-Cadherin, Vimentin), angiogenesis- (vascular endothelial growth factor (VEGF)), and apoptosis-related factors (cleaved Caspase-3, B-cell lymphoma-2 (Bcl-2), Bcl-2-associated X protein (Bax)) were quantified by quantitative real-time polymerase chain reaction or Western blot. TYMS was high-expressed yet miR-140-3p was low-expressed in LUAD cells. Upregulation of miR-140-3p inhibited TYMS expression, viability, colony formation, migration, invasion, and tube length within LUAD cells, while downregulation of miR-140-3p did oppositely. Silenced TYMS, the downstream target gene of miR-140-3p, reversed the effects of miR-140-3p downregulation on TYMS expression, cell viability, colony formation, migration, invasion, and tube length as well as the metastasis-, apoptosis- and angiogenesis-related proteins in LUAD cells. Upregulation of miR-140-3p inhibited the proliferation, migration, invasion and angiogenesis of LUAD cells via targeting TYMS.Shanzhi WanZhimin LiuYang ChenZhitao MaiMingming JiangQingguo DiBaohua SunTaylor & Francis Grouparticlelung adenocarcinomamicrorna-140-3pproliferationmetastasisangiogenesisthymidylate synthetaseBiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic lung adenocarcinoma
microrna-140-3p
proliferation
metastasis
angiogenesis
thymidylate synthetase
Biotechnology
TP248.13-248.65
spellingShingle lung adenocarcinoma
microrna-140-3p
proliferation
metastasis
angiogenesis
thymidylate synthetase
Biotechnology
TP248.13-248.65
Shanzhi Wan
Zhimin Liu
Yang Chen
Zhitao Mai
Mingming Jiang
Qingguo Di
Baohua Sun
MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
description MicroRNA (miR)-140-3p has been proved to repress lung adenocarcinoma (LUAD), and our study aims to further evaluate the mechanism. Bioinformatic analyses were performed. The viability, proliferation, migration, invasion and angiogenesis of transfected LUAD cells were all determined via Cell Counting Kit-8, colony formation, Scratch, Transwell, and tube formation assays. The targeting relationship between miR-140-3p and Thymidylate Synthetase (TYMS) was confirmed by dual-luciferase reporter (DLR) assay. Relative expressions of miR-140-3p, TYMS, metastasis- (E-Cadherin, N-Cadherin, Vimentin), angiogenesis- (vascular endothelial growth factor (VEGF)), and apoptosis-related factors (cleaved Caspase-3, B-cell lymphoma-2 (Bcl-2), Bcl-2-associated X protein (Bax)) were quantified by quantitative real-time polymerase chain reaction or Western blot. TYMS was high-expressed yet miR-140-3p was low-expressed in LUAD cells. Upregulation of miR-140-3p inhibited TYMS expression, viability, colony formation, migration, invasion, and tube length within LUAD cells, while downregulation of miR-140-3p did oppositely. Silenced TYMS, the downstream target gene of miR-140-3p, reversed the effects of miR-140-3p downregulation on TYMS expression, cell viability, colony formation, migration, invasion, and tube length as well as the metastasis-, apoptosis- and angiogenesis-related proteins in LUAD cells. Upregulation of miR-140-3p inhibited the proliferation, migration, invasion and angiogenesis of LUAD cells via targeting TYMS.
format article
author Shanzhi Wan
Zhimin Liu
Yang Chen
Zhitao Mai
Mingming Jiang
Qingguo Di
Baohua Sun
author_facet Shanzhi Wan
Zhimin Liu
Yang Chen
Zhitao Mai
Mingming Jiang
Qingguo Di
Baohua Sun
author_sort Shanzhi Wan
title MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
title_short MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
title_full MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
title_fullStr MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
title_full_unstemmed MicroRNA-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting TYMS (Thymidylate Synthetase)
title_sort microrna-140-3p represses the proliferation, migration, invasion and angiogenesis of lung adenocarcinoma cells via targeting tyms (thymidylate synthetase)
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/339c2728e55e404388911ee22047dd0e
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