A single nucleotide polymorphism in the MMP-1 promoter is correlated with histological differentiation of gastric cancer

J Cancer Res Clin Oncol. 2004 May;130(5):259-65. doi: 10.1007/s00432-004-0543-1. Epub 2004 Feb 18.

Abstract

Purpose: Matrix metalloproteinase-1 (MMP-1) plays a key role in cancer invasion and metastasis by degradation of extracellular matrix (ECM) and basement membrane barriers. The 1G/2G single nucleotide polymorphism (SNP) in the MMP-1 promoter at position -1607 bp has been reported to affect the transcriptional activity. In the light of these findings, we investigated whether this SNP in the MMP-1 promoter is associated with the development, differentiation, and progression of gastric cancer.

Methods: The 215 gastric cancer patients and 166 controls were used in this study. The SNP of the MMP-1 promoter was analyzed by PCR-RFLP and sequencing. The genotype frequency was compared between cases and controls, and the association with clinicopathological parameters among cases was studied.

Results: The frequency of 1G/2G genotypes in gastric cancer patients was similar to those in controls (p=0.57). The degree of tumor invasion, the presence of lymph node metastasis, and clinical stage showed no significant association with the SNP. On the other hand, we found a significant association with histological differentiation and gender among gastric cancer patients (p<0.05, respectively).

Conclusions: The presence of 2G allele in the MMP-1 promoter did not enhance the risk of gastric cancer; however, it may be involved in differentiation of gastric cancer.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Case-Control Studies
  • Cell Differentiation*
  • DNA / genetics
  • Disease Progression
  • Female
  • Gene Expression Regulation, Enzymologic*
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Lymphatic Metastasis / genetics
  • Male
  • Matrix Metalloproteinase 1 / genetics*
  • Neoplasm Invasiveness / genetics
  • Neoplasm Staging
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single Nucleotide / genetics*
  • Promoter Regions, Genetic / genetics*
  • Stomach Neoplasms / enzymology
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology

Substances

  • DNA
  • Matrix Metalloproteinase 1