Lee Amy S
Department of Biochemistry and Molecular Biology, University of Southern California/Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, 1441 Eastlake Avenue, Los Angeles, CA 90089, USA.
Cancer Res. 2007 Apr 15;67(8):3496-9. doi: 10.1158/0008-5472.CAN-07-0325.
Cancer cells adapt to chronic stress in the tumor microenvironment by inducing the expression of GRP78/BiP, a major endoplasmic reticulum chaperone with Ca(2+)-binding and antiapoptotic properties. GRP78 promotes tumor proliferation, survival, metastasis, and resistance to a wide variety of therapies. Thus, GRP78 expression may serve as a biomarker for tumor behavior and treatment response. Combination therapy suppressing GRP78 expression may represent a novel approach toward eradication of residual tumors. Furthermore, the recent discovery of GRP78 on the cell surface of cancer cells but not in normal tissues suggests that targeted therapy against cancer via surface GRP78 may be feasible.
癌细胞通过诱导GRP78/BiP的表达来适应肿瘤微环境中的慢性应激,GRP78/BiP是一种主要的内质网伴侣蛋白,具有钙离子结合和抗凋亡特性。GRP78促进肿瘤增殖、存活、转移以及对多种疗法的抗性。因此,GRP78的表达可能作为肿瘤行为和治疗反应的生物标志物。抑制GRP78表达的联合疗法可能代表一种根除残留肿瘤的新方法。此外,最近发现在癌细胞而非正常组织的细胞表面存在GRP78,这表明通过靶向癌细胞表面的GRP78进行治疗可能是可行的。