Kim Seok-Hyun, Ricci M Stacey, El-Deiry Wafik S
Laboratory of Molecular Oncology and Cell Cycle Regulation, Department of Medicine, Institute for Translational Medicine and Therapeutics, Abramson Comprehensive Cancer Center, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Cancer Res. 2008 Apr 1;68(7):2062-4. doi: 10.1158/0008-5472.CAN-07-6278.
The proapoptotic cytokine tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is being evaluated presently as a selective anticancer agent, but its limited effects against cancer cell lines has raised some concerns about its ultimate clinical utility. Here, we review recent findings that cancer cell sensitivity to TRAIL is greatly increased when the Bcl-2 family protein Mcl-1 is down-regulated by the Raf/vascular endothelial growth factor kinase inhibitor sorafenib, a Food and Drug Administration-approved cancer drug. Using the TRAIL-sorafenib combination as a tactic to more effectively kill cancer cells may provide an effective tool to attack a variety of human cancers that are largely presently untreatable.
促凋亡细胞因子肿瘤坏死因子相关凋亡诱导配体(TRAIL)目前正作为一种选择性抗癌药物进行评估,但其对癌细胞系的有限作用引发了人们对其最终临床效用的一些担忧。在此,我们回顾了近期的研究发现,即当Bcl-2家族蛋白Mcl-1被美国食品药品监督管理局批准的抗癌药物、Raf/血管内皮生长因子激酶抑制剂索拉非尼下调时,癌细胞对TRAIL的敏感性会大大增加。将TRAIL-索拉非尼联合使用作为一种更有效杀死癌细胞的策略,可能为攻克目前基本上无法治疗的多种人类癌症提供一种有效工具。