Construction of cDNA representational difference analysis based on two cDNA libraries and identification of garlic inducible expression genes in human gastric cancer cells

World J Gastroenterol. 2002 Apr;8(2):208-12. doi: 10.3748/wjg.v8.i2.208.

Abstract

Aim: To elucidate molecular mechanism of chemopreventive efficacies of garlic against human gastric cancer (HGC).

Methods: HGC cell line BGC823 was treated with Allitridi (a kind of garlic extract) and Allitridi-treated and parental BGC823 cDNA libraries were constructed respectively by using lambdaZAP II vector. cDNA Representational Difference Analysis (cDNA RDA) was performed using Bam H I cutting-site and abundant cDNA messages provided by the libraries. Northern blot analysis was applied to identify the obtained difference products.

Results: Two specific cDNA fragments were obtained and characterized to be derived from homo sapiens folate receptor alpha (FRalpha) gene and calcyclin gene respectively. Northern blot results showed a 4-fold increase in FRalpha gene expression level and 9-fold increase in calcyclin mRNA level in BGC823 cells after Allitridi treatment for 72h.

Conclusion: The method of cDNA RDA based on cDNA libraries combines the high specificity of cDNA RDA with abundant cDNA messages in cDNA library; this expands the application of cDNA library and increases the specificity of cDNA RDA. Up-regulation of FRalpha gene and calcyclin gene expressions induced by Allitridi provide valuable molecular evidence for the efficacy garlic in treating HGC as well as other diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allyl Compounds / pharmacology*
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cell Cycle Proteins*
  • Cell Size
  • Folate Receptors, GPI-Anchored
  • Garlic / chemistry*
  • Gene Expression Regulation, Neoplastic*
  • Gene Library
  • Humans
  • Receptors, Cell Surface*
  • S100 Calcium Binding Protein A6
  • S100 Proteins / genetics*
  • S100 Proteins / metabolism
  • Sequence Analysis, DNA* / methods
  • Stomach Neoplasms / genetics*
  • Sulfides / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Allyl Compounds
  • Carrier Proteins
  • Cell Cycle Proteins
  • Folate Receptors, GPI-Anchored
  • Receptors, Cell Surface
  • S100 Calcium Binding Protein A6
  • S100 Proteins
  • Sulfides
  • diallyl trisulfide
  • S100A6 protein, human