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硬脂酰辅酶A去饱和酶1通过使AMPK信号通路失活,对人肝细胞癌中自噬诱导的细胞死亡起负调控作用。

SCD1 negatively regulates autophagy-induced cell death in human hepatocellular carcinoma through inactivation of the AMPK signaling pathway.

作者信息

Huang Guang-Ming, Jiang Qing-Hu, Cai Can, Qu Mei, Shen Wei

机构信息

Department of Gastroenterology and Hepatology, Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.

Department of Hepatobiliary Surgery, Dazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, Sichuan 635000, China.

出版信息

Cancer Lett. 2015 Mar 28;358(2):180-190. doi: 10.1016/j.canlet.2014.12.036. Epub 2014 Dec 17.

Abstract

Stearoyl-CoA desaturase 1 (SCD1) is a key regulator in the mechanisms of cell proliferation, survival and transformation to cancer, and autophagy also plays a critical role in hepatocellular carcinoma (HCC). However, whether SCD1 mediates autophagy in HCC remains unknown. In this study, we observed significantly elevated SCD1 expression levels and evident suppression of autophagy in HCC, and the positive SCD1 expression and autophagy defect were independently correlated with poor prognosis of HCC patients. We also found that the inhibition of SCD1 by a pharmacological inhibitor reduced cell viability and induced apoptosis and autophagy of human HCC cells in a dose- and time-dependent manner. Moreover, the pharmacological inhibition of AMPK supported the hypothesis that the induction of autophagy caused by SCD1 inhibition relied on AMPK stimulation. Furthermore, the human HCC cells death triggered by inhibition of SCD1 was partly involved in autophagy-induced apoptosis via AMPK signaling. Our findings reveal a novel role for SCD1 in the regulation of autophagy via AMPK signaling and provide mechanistic input for the clinical exploration that the combination of SCD1 inhibition with autophagy induction may be attractive for the management of HCC.

摘要

硬脂酰辅酶A去饱和酶1(SCD1)是细胞增殖、存活及向癌症转化机制中的关键调节因子,自噬在肝细胞癌(HCC)中也起着关键作用。然而,SCD1是否介导HCC中的自噬仍不清楚。在本研究中,我们观察到HCC中SCD1表达水平显著升高且自噬明显受到抑制,SCD1阳性表达和自噬缺陷与HCC患者的不良预后独立相关。我们还发现,用药物抑制剂抑制SCD1可降低细胞活力,并以剂量和时间依赖性方式诱导人HCC细胞凋亡和自噬。此外,对AMPK的药物抑制支持了以下假设:SCD1抑制诱导的自噬依赖于AMPK刺激。此外,抑制SCD1引发的人HCC细胞死亡部分通过AMPK信号传导参与自噬诱导的凋亡。我们的研究结果揭示了SCD1在通过AMPK信号传导调节自噬中的新作用,并为临床探索提供了机制依据,即抑制SCD1与诱导自噬相结合可能对HCC的治疗具有吸引力。

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