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内质网应激介导的人肝细胞癌抗癌活性的易感因素解析。

Elucidation of susceptible factors to endoplasmic reticulum stress-mediated anticancer activity in human hepatocellular carcinoma.

作者信息

Chiang Po-Cheng, Hsu Jui-Ling, Yeh Ting-Chun, Pan Shiow-Lin, Guh Jih-Hwa

机构信息

School of Pharmacy, National Taiwan University, Taipei, Taiwan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2008 Apr;377(2):167-77. doi: 10.1007/s00210-007-0249-4. Epub 2008 Jan 29.

Abstract

The initiation of endoplasmic reticulum (ER) stress has been suggested to play potential roles in hepatocarcinogenesis. However, many obstacles remain as to whether ER stress plays a role in carcinogenesis or tumoricide. This study sought to identify the signals that can serve as anticancer effectors in cells in response to ER stress. Tunicamycin (an N-glycosylation inhibitor) inhibited cell proliferation with IC(50) values of 0.19 and 0.62 microg/ml in hepatoma (Hep) 3B and HepG2 cells, respectively. It induced G1 arrest of the cell cycle in both cell lines. The anticancer mechanism of tunicamycin was investigated in Hep3B cells. Tunicamycin induced a rapid decline of cyclin D1 and cyclin A expression and an early increase of glucose-related protein (GRP) 78 and growth arrest and DNA damage-inducible transcription factor (GADD) 153 levels. Cyclin A was the most sensitive regulator to tunicamycin-triggered degradation mechanism. The association of p27(Kip1) with cyclin D1/cyclin-dependent kinase (Cdk) 4 was also increased by tunicamycin. The inhibition of GADD153 expression by transfection of GADD153 antisense did not modify tunicamycin-induced G1 arrest and cyclin/Cdk expressions. The knockdown of GRP78 expression by the siRNA transfection technique moderately increased tunicamycin-induced apoptosis but not the antiproliferative effect by sulforhodamine B assay. We suggest that tunicamycin induces G1 arrest through down-regulation of cyclins and Cdks, in which cyclin A is more susceptible to ER stress-triggered degradation mechanism in Hep3B cells. The increased association of p27(Kip1) with cyclin D1/Cdk4 may also contribute to tunicamycin-induced cell-cycle arrest. GADD153 and GRP78 play a minor role in tunicamycin-mediated antiproliferative effect, although GRP78 moderately inhibits apoptosis in Hep3B cells. These data provide evidence that cell-cycle regulators are susceptible factors in hepatocellular carcinoma (HCC) responsive to ER stress.

摘要

内质网(ER)应激的启动被认为在肝癌发生过程中发挥潜在作用。然而,关于ER应激在致癌或杀瘤过程中是否起作用仍存在许多障碍。本研究旨在确定在细胞中响应ER应激时可作为抗癌效应器的信号。衣霉素(一种N-糖基化抑制剂)在肝癌(Hep)3B和HepG2细胞中分别以0.19和0.62μg/ml的IC(50)值抑制细胞增殖。它在两种细胞系中均诱导细胞周期的G1期阻滞。在Hep3B细胞中研究了衣霉素的抗癌机制。衣霉素诱导细胞周期蛋白D1和细胞周期蛋白A表达迅速下降,以及葡萄糖相关蛋白(GRP)78和生长停滞及DNA损伤诱导转录因子(GADD)153水平早期升高。细胞周期蛋白A是对衣霉素触发的降解机制最敏感的调节因子。衣霉素还增加了p27(Kip1)与细胞周期蛋白D1/细胞周期蛋白依赖性激酶(Cdk)4的结合。通过转染GADD153反义核酸抑制GADD153表达并未改变衣霉素诱导的G1期阻滞和细胞周期蛋白/Cdk表达。通过小干扰RNA转染技术敲低GRP78表达适度增加了衣霉素诱导的凋亡,但通过磺酰罗丹明B测定法并未增加其抗增殖作用。我们认为衣霉素通过下调细胞周期蛋白和Cdk诱导G1期阻滞,其中细胞周期蛋白A在Hep3B细胞中更易受到ER应激触发的降解机制影响。p27(Kip1)与细胞周期蛋白D1/Cdk4结合增加也可能有助于衣霉素诱导的细胞周期阻滞。GADD153和GRP78在衣霉素介导的抗增殖作用中起次要作用,尽管GRP78适度抑制Hep3B细胞中的凋亡。这些数据提供了证据,表明细胞周期调节因子是肝细胞癌(HCC)中对ER应激有反应的敏感因素。

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