Related Experiment Video
Updated: Sep 20, 2026

Modeling Colitis-Associated Cancer with Azoxymethane (AOM) and Dextran Sulfate Sodium (DSS)
Published on: September 11, 2012
Susceptibility to Ulcerative Colitis and Genetic Polymorphisms of A251G SOD1 and C-262T CAT
Gadier El-Kheshen1, Maryam Moeini2, Mostafa Saadat1
1Department of Biology, College of Sciences, Shiraz University, Shiraz, Iran.
Background:
Reactive oxygen species can attack and damage almost every molecule found in living cells, including proteins, carbohydrates, lipids, and DNA. For this reason, their production is normally tightly controlled. Among the most important defenses against these radicals are the superoxide dismutase (SOD) enzymes and catalase (CAT). Increasing attention has been given to the role of reactive oxygen metabolites in the pathogenesis of ulcerative colitis (UC), which is defined as an idiopathic and chronic intestinal inflammation. Accordingly, we hypothesized a relation between genetic polymorphisms in the two antioxidant enzymes SOD1 A251G (rs2070424) and CAT C-262T (rs1001179) and the risk of UC.
Methods:
The present case-control study included 109 UC patients (46 males and 50 females) and 186 (67 males and 119 females) gender-matched healthy controls. Genotyping was done by the PCR-RFLP method.
Results:
After adjusting for age and gender, a significant association was observed between the AG+GG genotypes of SOD1 A251G polymorphism (vs. AA genotype) and risk of UC (OR=0.29, 95% CI: 0.10-0.86, P= 0.025) after adjusting for age and gender. Our statistical analysis revealed that the CAT C-262T polymorphism did not associate with the risk of UC before and/or after adjusting for age and gender.
Conclusions:
Based on the present statistical analysis, the G allele of the SOD1 A251G polymorphism decreases the risk of UC, thus it might be assumed that the G allele has a protective role.
Insights
The G allele of the superoxide dismutase 1 (SOD1) A251G polymorphism may protect against ulcerative colitis (UC). The catalase (CAT) C-262T polymorphism showed no association with UC risk in this study.
Area of Science:
- Genetics and Molecular Biology
- Gastroenterology
- Oxidative Stress Research
Background:
- Reactive oxygen species (ROS) can damage cellular components, necessitating robust antioxidant defenses.
- Superoxide dismutase (SOD) and catalase (CAT) are key enzymes in combating ROS.
- The role of ROS in ulcerative colitis (UC) pathogenesis is increasingly recognized.
Purpose of the Study:
- To investigate the association between genetic polymorphisms in SOD1 (A251G) and CAT (C-262T) and the risk of developing UC.
- To explore the potential protective role of antioxidant enzyme gene variants against UC.
Main Methods:
- A case-control study involving 109 UC patients and 186 healthy controls.
- Genotyping of SOD1 A251G (rs2070424) and CAT C-262T (rs1001179) polymorphisms using PCR-RFLP.
- Statistical analysis adjusted for age and gender.
Main Results:
- The AG+GG genotypes of the SOD1 A251G polymorphism were significantly associated with a decreased risk of UC (OR=0.29, P=0.025).
- The G allele of SOD1 A251G was linked to a reduced risk of UC.
- No significant association was found between the CAT C-262T polymorphism and UC risk.
Conclusions:
- The G allele of the SOD1 A251G polymorphism appears to have a protective effect against ulcerative colitis.
- These findings suggest a potential role for SOD1 genetic variants in UC susceptibility.
- Further research is warranted to elucidate the precise mechanisms.
Related Concept Videos
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Inflammatory Bowel Disease II: Ulcerative Colitis
Inflammatory Bowel Disease III: Crohn's Disease

