| Literature DB >> 18381408 |
Seok-Hyun Kim1, M Stacey Ricci, Wafik S El-Deiry.
Abstract
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.Entities:
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Year: 2008 PMID: 18381408 DOI: 10.1158/0008-5472.CAN-07-6278
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701