Phenotype 2 of deoxyribonuclease I may be used as a risk factor for gastric carcinoma

Cancer. 1998 May 1;82(9):1621-5. doi: 10.1002/(sici)1097-0142(19980501)82:9<1621::aid-cncr4>3.0.co;2-d.

Abstract

Background: Human deoxyribonuclease I (DNase I) (EC3.1.21.1) is one of the candidate nucleases that acts in mammalian cells during apoptosis. Genetic polymorphism of DNase I has been classified into 15 phenotypes controlled by 5 autosomal codominant alleles. The purpose of this study was to determine whether DNase I polymorphism is closely related to the incidence of gastric carcinoma.

Methods: The phenotype distribution was examined using urine samples obtained from unrelated Japanese patients with gastric carcinoma (n = 97) and benign gastric diseases (n = 76). Phenotyping was performed using isoelectric focusing electrophoresis in thin polyacrylamide gel and immunoblotting with an antihuman DNase I antibody.

Results: A close statistical association was found between patients with gastric carcinoma and a high frequency of DNase I phenotype 2. However, there was no significant difference in the phenotype distribution between the group of patients with benign gastric diseases and the controls.

Conclusions: The findings of the current study suggest that DNase I phenotype 2 may be a marker for gastric carcinoma. Therefore, compared with other phenotypes, DNase I phenotype 2 may have potential for identifying patients who are at risk of harboring or developing gastric carcinoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma / enzymology*
  • Carcinoma / genetics
  • Deoxyribonuclease I / genetics
  • Deoxyribonuclease I / physiology*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Phenotype
  • Polymorphism, Genetic
  • Risk Factors
  • Stomach Diseases / enzymology
  • Stomach Diseases / genetics
  • Stomach Neoplasms / enzymology*
  • Stomach Neoplasms / genetics

Substances

  • Deoxyribonuclease I