Human CD34+ cells engineered to express membrane-bound tumor necrosis factor-related apoptosis-inducing ligand target both tumor cells and tumor vasculature

Blood. 2010 Mar 18;115(11):2231-40. doi: 10.1182/blood-2009-08-239632. Epub 2010 Jan 14.

Abstract

Adenovirus-transduced CD34+ cells expressing membrane-bound tumor necrosis factor-related apoptosis-inducing ligand (CD34-TRAIL+ cells) exert potent antitumor activity. To further investigate the mechanism(s) of action of CD34-TRAIL+ cells, we analyzed their homing properties as well as antitumor and antivascular effects using a subcutaneous myeloma model in immunodeficient mice. After intravenous injection, transduced cells homed in the tumor peaking at 48 hours when 188 plus or minus 25 CD45+ cells per 10(5) tumor cells were detected. Inhibition experiments showed that tumor homing of CD34-TRAIL+ cells was largely mediated by vascular cell adhesion molecule-1 and stromal cell-derived factor-1. Both CD34-TRAIL+ cells and soluble (s)TRAIL significantly reduced tumor volume by 40% and 29%, respectively. Computer-aided analysis of TdT-mediated dUTP nick end-labeling-stained tumor sections demonstrated significantly greater effectiveness for CD34-TRAIL+ cells in increasing tumor cell apoptosis and necrosis over sTRAIL. Proteome array analysis indicated that CD34-TRAIL+ cells and sTRAIL activate similar apoptotic machinery. In vivo staining of tumor vasculature with sulfosuccinimidyl-6-(biotinamido) hexanoate-biotin revealed that CD34-TRAIL+ cells but not sTRAIL significantly damaged tumor vasculature, as shown by TdT-mediated dUTP nick end-labeling+ endothelial cells, appearance of hemorrhagic areas, and marked reduction of endothelial area. These results demonstrate that tumor homing of CD34-TRAIL+ cells induces early vascular disruption, resulting in hemorrhagic necrosis and tumor destruction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD34 / metabolism*
  • Apoptosis
  • Blood Vessels / metabolism
  • Blood Vessels / pathology
  • Cell Line, Tumor
  • Cell Membrane / metabolism*
  • Cell Transplantation
  • Chemokine CXCL12 / metabolism
  • Genetic Engineering*
  • Hemorrhage / pathology
  • Humans
  • Mice
  • Necrosis
  • Neoplasms / blood supply*
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • Neovascularization, Pathologic / pathology
  • Neovascularization, Pathologic / therapy
  • Protein Binding
  • TNF-Related Apoptosis-Inducing Ligand / metabolism*
  • Tissue Distribution
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Antigens, CD34
  • Chemokine CXCL12
  • TNF-Related Apoptosis-Inducing Ligand
  • Vascular Cell Adhesion Molecule-1