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木樨草素通过上调 miR-203 表现出抗乳腺癌特性。

Luteolin exhibits anti-breast cancer property through up-regulating miR-203.

机构信息

a Department of Galactophore, Linyi Central Hospital , Linyi , PR China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3265-3271. doi: 10.1080/21691401.2019.1646749.

Abstract

Luteolin is a representative of natural flavonoid that has anti-tumour properties. This study designed to check its impact on breast cancer and the underlying mechanisms. MDA-MB-453 and MCF-7 cells were administrated with luteolin and the following techniques were carried out: CCK-8 assay, FITC-PI double-staining and Western blot. qRT-PCR analysis was utilized to see the effects of luteolin on miR-203 expression. Besides, miR-203 expression was silenced by transfection with specific inhibitor. Luteolin remarkably declined MDA-MB-453 and MCF-7 cells viability and accelerated apoptosis which accompanied by Bax up-regulation, Bcl-2 down-regulation and Caspase-3 cleavage. Also, luteolin impeded TGFβ1-induced EMT, as evidenced by the decreased levels of Vimentin, Zeb1 and N-cadherin, as well as the increased level of E-cadherin. miR-203 was highly expressed in 22 pair of breast cancer tissues than the matched paracancerous tissues. Luteolin could elevate miR-203 level. Besides, luteolin's anti-tumour effects were partially eliminated by miR-203 silence. Further, luteolin inhibited Ras/Raf/MEK/ERK signalling, while the inhibitory effects were flattened by miR-203 silence. Luteolin significantly reduced breast cancer cells growth and EMT. Luteolin exerted its anti-tumour effects possibly involved the elevated expression of miR-203 and the inhibited Ras/Raf/MEK/ERK signalling.

摘要

木犀草素是具有抗肿瘤特性的天然类黄酮的代表。本研究旨在检查其对乳腺癌的影响及其潜在机制。用木犀草素处理 MDA-MB-453 和 MCF-7 细胞,并进行以下技术操作:CCK-8 测定、FITC-PI 双染和 Western blot。qRT-PCR 分析用于观察木犀草素对 miR-203 表达的影响。此外,通过转染特异性抑制剂沉默 miR-203 的表达。木犀草素显著降低 MDA-MB-453 和 MCF-7 细胞活力并加速细胞凋亡,伴随着 Bax 上调、Bcl-2 下调和 Caspase-3 切割。此外,木犀草素抑制 TGFβ1 诱导的 EMT,表现为波形蛋白、Zeb1 和 N-钙粘蛋白水平降低,以及 E-钙粘蛋白水平升高。22 对乳腺癌组织中 miR-203 的表达明显高于配对癌旁组织。木犀草素可以提高 miR-203 的水平。此外,miR-203 沉默部分消除了木犀草素的抗肿瘤作用。此外,木犀草素抑制 Ras/Raf/MEK/ERK 信号通路,而 miR-203 沉默则使抑制作用变平。木犀草素显著抑制乳腺癌细胞生长和 EMT。木犀草素发挥其抗肿瘤作用可能涉及 miR-203 的高表达和 Ras/Raf/MEK/ERK 信号通路的抑制。

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