Endometriosis Knowledgebase


A repository for genes associated with endometriosis

Results


PMID 22653586
Gene Name TP53
Condition Endometriosis
Association Associated
Mutation Pro/Pro of codon 72 polymorphism in TP53
Population size 386
Population details 386 (235 healthy Mexican women (controls with surgically excluded endometriosis), 151 Mexican women with endometriosis)
Sex Female
Other associated phenotypes Endometriosis
Association of TP53 gene codon 72 polymorphism with endometriosis in Mexican women.

Genet Mol Res. 2012 May 15;11(2):1401-8. doi: 10.4238/2012.May.15.10.

Gallegos-Arreola, M P| Figuera-Villanueva, L E| Puebla-Perez, A M| Montoya-Fuentes, H| Suarez-Rincon, A E| Zuniga-Gonzalez, G M

Molecular Medicine Department, Biomedical Research Center West, Instituto Mexicano del Seguro Social, Guadalajara, Mexico. patrici0803@yahoo.com.mx

The TP53 tumor suppressor gene plays an important role in cell cycle regulation; polymorphisms of this gene have been associated with endometriosis. We examined the role of TP53 codon 72 polymorphism by comparing genotypes of 235 healthy Mexican women (controls with surgically excluded endometriosis) with the genotypes of 151 Mexican women with endometriosis. The observed genotype frequencies for controls and endometriosis patients were 8 and 22% for proline/proline (Pro/Pro), 30 and 34% for proline/arginine (Pro/Arg), and 62 and 44% for arginine/arginine (Arg/Arg), respectively. We found that odds ratio (OR) = 3.3; 95% confidence intervals (95%CI) = 1.7-6.4; P = 0.0001. The association was also evident in the comparison of the distributions of genotypes Pro/Pro and Pro/Arg in patients with moderate-to-severe endometriosis; OR = 1.9; 95%CI = 0.95-3.9; P = 0.049. We suggest that genotype Pro/Pro of codon 72 polymorphism in TP53 contributes significantly to endometriosis susceptibility in the Mexican population.

Mesh Terms: Codon/genetics| Endometriosis/*genetics| Female| Gene Frequency/genetics| Genes, p53/*genetics| Genetic Predisposition to Disease/genetics| Genotype| Humans| Mexico| Polymorphism, Genetic/*genetics|DA 2012/09/28 06:00