[Effect of expression of coxsackie and adenovirus receptor on antitumor activity of genetically modified adenovirus]

Ai Zheng. 2005 Apr;24(4):502-5.
[Article in Chinese]

Abstract

Background & objective: The effect of adenovirus, a kind of oncolytic virus and a kind of carrier in gene therapy, depends on the expression of Coxsackie and adenovirus receptor (CAR) on cell surface to a large degree. This study was to evaluate relationship of CAR expression to infectivity and efficacy of adenovirus.

Methods: Pathologic specimens from 29 patients in a clinical trial of genetically modified adenovirus (H101) were collected. Expression of CAR in cancer tissues was detected by immuohistochemistry. Expression of CAR on cancer cell membrane was detected by flow cytometry (FCM). Inhibitory effect of H101 on cells was assessed by MTT assay.

Results: Positive rate of CAR was significantly higher in patients achieved complete remission (CR) or partial remission (PR) than in patients had stable disease (SD) or progressive disease (PD) [70.0% (7/10) vs. 31.6% (6/19), P=0.048]. CAR expression on different cells was different, and the amount of CAR was positively related to virus infectivity, presented as the inhibitory rate of H101-infected cells (r=0.986).

Conclusions: The expression of CAR closely relates to antitumor activity and efficacy of adenovirus. Also, the efficacy of adenovirus is higher on cancers with increased CAR expression than on those with decreased CAR expression.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Adenoviridae / physiology*
  • Adolescent
  • Adult
  • Aged
  • Cell Line, Tumor / metabolism
  • Cell Line, Tumor / virology
  • Cell Proliferation
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / therapy
  • Esophageal Neoplasms / virology
  • Female
  • Genetic Engineering
  • Genetic Therapy*
  • Humans
  • Male
  • Melanoma / metabolism
  • Melanoma / therapy
  • Melanoma / virology
  • Middle Aged
  • Nasopharyngeal Neoplasms / metabolism*
  • Nasopharyngeal Neoplasms / therapy
  • Nasopharyngeal Neoplasms / virology
  • Receptors, Virus / metabolism*
  • Remission Induction

Substances

  • CLMP protein, human
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Receptors, Virus