Mcl-1: a gateway to TRAIL sensitization.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 18381408.
- Also identified by DOI 10.1158/0008-5472.CAN-07-6278.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Neoplasm Proteins
- Neoplasms
- Proto-Oncogene Proteins c-bcl-2
- TNF-Related Apoptosis-Inducing Ligand