Anti-CD26 monoclonal antibody-mediated G1-S arrest of human renal clear cell carcinoma Caki-2 is associated with retinoblastoma substrate dephosphorylation, cyclin-dependent kinase 2 reduction, p27(kip1) enhancement, and disruption of binding to the extracellular matrix

Clin Cancer Res. 2006 Jun 1;12(11 Pt 1):3470-7. doi: 10.1158/1078-0432.CCR-06-0361.

Abstract

Purpose: CD26 is a 110-kDa cell surface glycoprotein with a role in tumor development through its association with key intracellular proteins. In this report, we show that binding of soluble anti-CD26 monoclonal antibody (mAb) inhibits the growth of the human renal carcinoma cells in both in vitro and in vivo experiments.

Experimental design: Growth inhibition by anti-CD26 mAb was assessed using proliferation assay and cell cycle analysis. Anti-CD26 mAb, chemical inhibitors, dominant-negative, or constitutively active forms of specific signaling molecules were used to evaluate CD26-associated pathways. The in vivo growth-inhibitory effect of anti-CD26 mAb was also assessed in a human renal carcinoma mouse xenograft model.

Results: In vitro experiments show that anti-CD26 mAb induces G1-S cell cycle arrest associated with enhanced p27(kip1) expression, down-regulation of cyclin-dependent kinase 2, and dephosphorylation of retinoblastoma substrate. Moreover, our data show that enhanced p27(kip1) expression is dependent on the attenuation of Akt activity. Anti-CD26 mAb also internalizes cell surface CD26, leading to decreased binding to collagen and fibronectin. Experiments with a mouse xenograft model involving human renal carcinoma cells show that anti-CD26 mAb treatment drastically inhibits tumor growth in tumor-bearing mice, resulting in enhanced survival.

Conclusions: Taken together, our data strongly suggest that anti-CD26 mAb treatment may have potential clinical use for CD26-positive renal cell carcinomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology*
  • Antibodies, Monoclonal / therapeutic use
  • Antigen-Antibody Reactions
  • Binding Sites
  • Carcinoma, Renal Cell / drug therapy
  • Carcinoma, Renal Cell / immunology*
  • Carcinoma, Renal Cell / pathology
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclin-Dependent Kinase 2 / metabolism*
  • Cyclin-Dependent Kinase Inhibitor p27 / biosynthesis
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism*
  • Dipeptidyl Peptidase 4 / biosynthesis
  • Dipeptidyl Peptidase 4 / immunology
  • Dipeptidyl-Peptidase IV Inhibitors*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism*
  • Female
  • G1 Phase / drug effects
  • Humans
  • Kidney Neoplasms / drug therapy
  • Kidney Neoplasms / immunology*
  • Kidney Neoplasms / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Phosphorylation / drug effects
  • Retinoblastoma Protein / metabolism*
  • S Phase / drug effects
  • Structure-Activity Relationship
  • Transplantation, Heterologous
  • Xenograft Model Antitumor Assays

Substances

  • Antibodies, Monoclonal
  • Dipeptidyl-Peptidase IV Inhibitors
  • Retinoblastoma Protein
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinase 2
  • Dipeptidyl Peptidase 4