A 71-Gene Signature of TRAIL Sensitivity in Cancer Cells

Jun-Jie Chen, Steen Knudsen, Wiktor Mazin, Jesper Dahlgaard, Baolin Zhang

Publikation: Bidrag til tidsskriftTidsskriftsartikelForskningpeer review

Abstract

TNF-related apoptosis inducing ligand (TRAIL) is a promising anticancer agent because of its ability to selectively induce apoptosis in cancer cells but not in most normal cells. However, some cancer cells are resistant to TRAIL cytotoxicity thereby limiting its therapeutic efficacy. Using genome-wide mRNA expression profiles from the NCI60 panel and their differential sensitivities to TRAIL-induced apoptosis, we have identified 71 genes whose expression levels are systemically higher in TRAIL-sensitive cell lines than resistant lines. The elevated expression of the 71 genes was able to accurately predict TRAIL sensitivity in the NCI60 training set and two test sets consisting of a total of 95 human cancer cell lines. Interestingly, the 71-gene signature is dominated by two functionally related gene families-interferon (IFN)-induced genes and the MHC genes. Consistent with this result, treatment with IFN-γ augmented TRAIL-induced apoptosis. The 71-gene signature could be evaluated clinically for predicting tumor response to TRAIL-related therapies. Mol Cancer Ther; 11(1); 34-44. ©2011 AACR.
OriginalsprogEngelsk
TidsskriftMolecular Cancer Therapeutics
Vol/bind11
Udgave nummer1
ISSN1535-7163
DOI
StatusUdgivet - 2012
Udgivet eksterntJa

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