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MicroRNA-760 通过调控 Notch1/Hes1-PTEN/Akt 信号通路抑制肝癌多柔比星耐药。

MicroRNA-760 Inhibits Doxorubicin Resistance in Hepatocellular Carcinoma through Regulating Notch1/Hes1-PTEN/Akt Signaling Pathway.

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, P.R. China.

Clinical Research Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, P.R. China.

出版信息

J Biochem Mol Toxicol. 2018 Aug;32(8):e22167. doi: 10.1002/jbt.22167. Epub 2018 Jul 3.

Abstract

Accumulating studies have suggested that microRNA-760 (miR-760) plays an important role in chemoresistance of various cancer cells. However, whether miR-760 regulates the chemoresistance of hepatocellular carcinoma (HCC) remains unclear. In this study, we found that miR-760 was decreased in HCC cell lines, and doxorubicin (Dox) treatment significantly decreased miR-760 expression in HCC cells. Overexpression of miR-760 sensitized HCC cells to Dox-induced cytotoxicity and apoptosis, whereas miR-760 inhibition showed the opposite effects. Notch1 was predicted as a target gene of miR-760. miR-760 negatively regulated Notch1 expression and Notch1/Hes1 signaling. Overexpression of miR-760 increased PTEN expression and decreased the phosphorylation of Akt. Activation of Notch signaling significantly reversed the inhibitory effect of miR-760 on Dox-resistance and abrogated the effect of miR-760 on the PTEN/Akt signaling pathway in HCC cells. Overall, our results demonstrate that miR-760 inhibits Dox-resistance in HCC cells through inhibiting Notch1 and promoting PTEN expression.

摘要

越来越多的研究表明 microRNA-760(miR-760)在各种癌细胞的化疗耐药中发挥着重要作用。然而,miR-760 是否调节肝癌(HCC)的化疗耐药性尚不清楚。在本研究中,我们发现 miR-760 在 HCC 细胞系中表达降低,阿霉素(Dox)处理显著降低 HCC 细胞中 miR-760 的表达。miR-760 的过表达使 HCC 细胞对 Dox 诱导的细胞毒性和细胞凋亡敏感,而 miR-760 的抑制则产生相反的效果。Notch1 被预测为 miR-760 的靶基因。miR-760 负调控 Notch1 表达和 Notch1/Hes1 信号通路。miR-760 的过表达增加了 PTEN 的表达,并降低了 Akt 的磷酸化。Notch 信号的激活显著逆转了 miR-760 对 Dox 耐药性的抑制作用,并消除了 miR-760 对 HCC 细胞中 PTEN/Akt 信号通路的影响。总的来说,我们的研究结果表明,miR-760 通过抑制 Notch1 并促进 PTEN 表达来抑制 HCC 细胞的 Dox 耐药性。

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