首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >The role of curcumae rhizoma-sparganii rhizoma medicated serum in epithelial-mesenchymal transition in the triple negative breast cancer Pharmacological role of CR-SR in the TBNC
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The role of curcumae rhizoma-sparganii rhizoma medicated serum in epithelial-mesenchymal transition in the triple negative breast cancer Pharmacological role of CR-SR in the TBNC

机译:CrcumaeRhizoma-Spariiha-Sparia-spargaii Rhizomate血清在TBNC中CR-SR三重阴性乳腺癌药理作用中的上皮间充质转换的作用

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摘要

The aim of this study was to investigate the effect of Curcumae Rhizoma-Sparganii Rhizoma (CR-SR) medicated serum on the changes of epithelial-mesenchymal transition (EMT) in the triple-negative breast cancer (TNBC). The EMT model was developed by using the TNBC MDA-MB-468 cells, which were treated with TGF-beta 1. The migration and invasion abilities of TGF-beta 1-treated MDA-MB-468 cells were detected by wound healing assay and transwell assay. Protein expression levels of E-cadherin and vimentin were determined by western blot. CR-SR medicated serum repressed the phenotypic transition in the TGF-beta 1-induced MDA-MB-468 cells. Moreover, CR-SR medicated serum inhibited TGF-beta 1-induced cell proliferation, migration and invasion. Besides, CR-SR medicated serum could reduce TGF-beta 1-induced up-regulation of the phosphorylation levels of Smad3, and reduce the expression of several transcription factors (Snail1, Snail2 and Twist1). CR-SR medicated serum might suppress TGF-beta 1-induced EMT in TNBC by decreasing the phosphorylated Smad3 (p-Smad3) pathway in vitro.
机译:本研究的目的是探讨CurcumaeRhizoma-Sparga-spariihia Rhizoma(Cr-SR)药物血清对三阴性乳腺癌(TNBC)中上皮 - 间充质转换(EMT)的影响的影响。通过使用TNBC MDA-MB-468细胞进行EMT模型,其用TGF-β1处理。通过伤口愈合测定检测TGF-Beta 1-处理的MDA-MB-468细胞的迁移和侵袭能力和伤口愈合测定Transwell测定。通过Western印迹测定E-Cadherin和Vimentin的蛋白表达水平。 CR-SR药物血清在TGF-β1诱导的MDA-MB-468细胞中抑制了表型转变。此外,CR-SR药物血清抑制TGF-β1诱导的细胞增殖,迁移和侵袭。此外,CR-SR药物血清可以降低TGF-β1-诱导Smad3的磷酸化水平的上调,并降低几种转录因子(Snail1,Snail2和Twist1)的表达。通过减少体外磷酸化的Smad3(P-Smad3)途径,Cr-SR药物血清可以抑制TNBC中的TGF-β1-诱导的EMT。

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