Adenoviral transduction efficiency of ovarian cancer cells can be limited by loss of integrin beta3 subunit expression and increased by reconstitution of integrin alphavbeta3

Hum Gene Ther. 2001 Mar 1;12(4):391-9. doi: 10.1089/10430340150504019.

Abstract

Recombinant adenoviruses expressing a therapeutic gene are currently used in clinical studies for treatment of advanced ovarian cancer. We therefore tested whether the expression level of primary (CAR) and secondary adenovirus receptors (integrins) was predictive of the efficacy of adenoviral gene transfer in ovarian cancer cells. Adenoviral transduction efficiency (ATE) was determined with an E1-deleted adenovirus type 5 expressing beta-galactosidase under a CMV promoter (AdGal). ATE was studied in relationship to the expression level of both CAR (coxsackie and adenovirus receptor) and integrins. A representative sample of 25 permanent human cell lines established from advanced ovarian cancer in our laboratory and the OV-2774 cell line were tested. Overall, ATE increased with increasing titers of AdGal. At a given titer of 50 infectious units per cell, transduction efficiency varied from 6 to 94% among the individual cell lines. All cell lines expressed CAR and integrin alpha(v)beta(5), but no relation between ATE and expression level of CAR or alpha(v)beta(5) integrin was observed. In contrast, cell lines with poor ATE, despite expressing high levels of CAR, lacked expression of integrins alpha(v)beta(3) and alpha(5)beta(1). Reconstitution of alpha(v)beta(3) integrin by reexpressing the beta(3) subunit significantly enhanced ATE of ovarian cancer cells. In ovarian cancer, neither integrins nor CAR alone appear to be potentially useful predictive markers for ATE by serotype 5 adenovirus in clinical gene therapy. A minimum level of CAR necessary for binding of adenoviruses was observed in all tested ovarian cancer cell lines. Loss of alpha(v)beta(3) integrin is frequently associated with advanced stages of ovarian cancer and can significantly reduce ATE.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Antigens, CD / biosynthesis*
  • Antigens, CD / genetics
  • Blotting, Western
  • Cell Membrane / metabolism
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • DNA Primers / chemistry
  • Female
  • Flow Cytometry
  • Gene Expression
  • Genetic Vectors
  • Humans
  • Integrin beta3
  • Integrins / analysis*
  • Neoplasm Proteins / analysis
  • Ovarian Neoplasms / metabolism*
  • Platelet Membrane Glycoproteins / biosynthesis*
  • Platelet Membrane Glycoproteins / genetics
  • RNA, Messenger / analysis
  • Receptors, Virus / metabolism
  • Receptors, Vitronectin / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transduction, Genetic*
  • Tumor Cells, Cultured
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Antigens, CD
  • CLMP protein, human
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • DNA Primers
  • Integrin beta3
  • Integrins
  • Neoplasm Proteins
  • Platelet Membrane Glycoproteins
  • RNA, Messenger
  • Receptors, Virus
  • Receptors, Vitronectin
  • beta-Galactosidase