Biomarkers for predicting the sensitivity of cancer cells to TRAIL-R1 agonistic monoclonal antibody

Cancer Lett. 2010 Jun 28;292(2):269-79. doi: 10.1016/j.canlet.2009.12.007. Epub 2010 Jan 6.

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and an agonistic monoclonal antibody to TRAIL-R1 (TRAIL-R1 mAb) induce apoptosis and show anti-proliferative activity in vitro and in vivo. However, some TRAIL-R1-expressing cell lines are not sensitive to either TRAIL-R1 mAb or TRAIL. We have identified four genes (STK17B, SP140L, CASP8, and AIM1) whose expression levels differ significantly between TRAIL-R1 mAb-sensitive and resistant cell lines. Using the expression levels of these genes, we predicted TRAIL-R1 mAb and TRAIL sensitivity in our test cell lines with 75% (9/12) and 84% (21/25) accuracy, respectively. Knockdown of STK17B in TRAIL-R1 mAb-sensitive cells augmented Bcl-2 expression and suppressed TRAIL-R1 mAb-induced apoptosis. Our results may be useful for predicting the response of cancers to TRAIL-agonistic drugs in the clinic.

MeSH terms

  • Antibodies, Monoclonal / immunology*
  • Biomarkers*
  • Blotting, Western
  • Cell Line, Tumor
  • Gene Knockdown Techniques
  • Humans
  • Polymerase Chain Reaction
  • Receptors, TNF-Related Apoptosis-Inducing Ligand / immunology*

Substances

  • Antibodies, Monoclonal
  • Biomarkers
  • Receptors, TNF-Related Apoptosis-Inducing Ligand