Northern Institute of Cancer Research and Newcastle Cancer Centre, Newcastle University, Newcastle upon Tyne, UK.
Pigment Cell Melanoma Res. 2010 Oct;23(5):675-82. doi: 10.1111/j.1755-148X.2010.00731.x. Epub 2010 Jul 12.
Targeting endoplasmic reticulum stress-induced apoptosis may offer an alternative therapeutic strategy for metastatic melanoma. Fenretinide and bortezomib induce apoptosis of melanoma cells but their efficacy may be hindered by the unfolded protein response, which promotes survival by ameliorating endoplasmic reticulum stress. The aim of this study was to test the hypothesis that inhibition of GRP78, a vital unfolded protein response mediator, increases cell death in combination with endoplasmic reticulum stress-inducing agents. Down-regulation of GRP78 by small-interfering RNA increased fenretinide- or bortezomib-induced apoptosis. Treatment of cells with a GRP78-specific subtilase toxin produced a synergistic enhancement with fenretinide or bortezomib. These data suggest that combining endoplasmic reticulum stress-inducing agents with strategies to down-regulate GRP78, or other components of the unfolded protein response, may represent a novel therapeutic approach for metastatic melanoma.
靶向内质网应激诱导的细胞凋亡可能为转移性黑色素瘤提供一种新的治疗策略。芬维 A 酯和硼替佐米诱导黑色素瘤细胞凋亡,但未折叠蛋白反应可能会阻碍其疗效,因为该反应通过改善内质网应激来促进细胞存活。本研究旨在验证以下假设,即抑制关键的未折叠蛋白反应介质 GRP78 与内质网应激诱导剂联合使用可增加细胞死亡。通过小干扰 RNA 下调 GRP78 可增加芬维 A 酯或硼替佐米诱导的细胞凋亡。用 GRP78 特异性枯草溶菌素毒素处理细胞可与芬维 A 酯或硼替佐米产生协同增强作用。这些数据表明,将内质网应激诱导剂与下调 GRP78 或未折叠蛋白反应的其他成分的策略相结合,可能为转移性黑色素瘤提供一种新的治疗方法。