Abstract |
The expression of growth factors, proteolytic enzymes, fibrogenic factors, and cytokines is altered in the Helicobacter pylori-infected gastric mucosa. Therefore, we aimed to evaluate the association of functional promoter variants of transforming growth factor (TGF)-B1 and matrix metalloproteinase (MMP)-7 genes with gastritis and gastric precancerous lesions. After upper gastrointestinal endoscopy, a total of 130 rapid urease test-positive patients with nonulcer dyspepsia were examined for H. pylori infection using modified Giemsa stain and IgG anti-CagA ELISA. All patients and 200 asymptomatic controls were genotyped for TGF-B1 (-509 C>T) and MMP-7 (-181 A>G) substitutions using PCR-RFLP. The genotype and allele frequencies of TGF-B1 and MMP-7 polymorphisms did not differ between patients and controls (p > 0.05). However, the CagA-positive patients with TGF-B1 -509 T allele had higher risk for gastric atrophy (p = 0.026, odds ratio [OR] = 2.38) and lymphoid follicle development (p = 0.028, OR = 2.29). In addition, CagA-positive patients carrying MMP-7 -181 G allele had risk for lymphoid follicle formation (p = 0.027, OR = 2.30). Thus, the present study revealed significant association of functional MMP-7 and TGF-B1 gene variants toward susceptibility to H. pylori-induced precancerous gastric lesions.
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Authors | B R Achyut, Uday C Ghoshal, Nikhil Moorchung, Balraj Mittal |
Journal | DNA and cell biology
(DNA Cell Biol)
Vol. 28
Issue 6
Pg. 295-301
(Jun 2009)
ISSN: 1557-7430 [Electronic] United States |
PMID | 19317620
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, Bacterial
- Bacterial Proteins
- Transforming Growth Factor beta1
- cagA protein, Helicobacter pylori
- MMP7 protein, human
- Matrix Metalloproteinase 7
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Topics |
- Adult
- Alleles
- Antigens, Bacterial
(analysis)
- Atrophy
- Bacterial Proteins
(analysis)
- Female
- Gastritis
(genetics, pathology)
- Genotype
- Helicobacter Infections
(genetics, pathology)
- Helicobacter pylori
- Humans
- Lymphoid Tissue
(pathology)
- Male
- Matrix Metalloproteinase 7
(genetics)
- Middle Aged
- Polymorphism, Single Nucleotide
- Precancerous Conditions
(genetics, microbiology, pathology)
- Promoter Regions, Genetic
(genetics)
- Risk
- Sequence Deletion
- Stomach
(pathology)
- Stomach Neoplasms
(epidemiology, microbiology)
- Transforming Growth Factor beta1
(genetics)
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