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pubmed-article:7640212pubmed:abstractTextThe isoenzyme Mu of glutathione S-transferase (GSTM1) is dominantly inherited, and the prevalence of this isoenzyme in the population is about 60%. The lack of GSTM1 has been linked with cancer risk. The frequency of the phenotypes of this isoenzyme in melanoma (MM) patients (n = 197) is reported here. A significantly higher proportion of individuals in the control group (n = 147) had measurable GSTM1 than MM patients (59.1% vs 42%, P = 0.002); there was a higher proportion of positive phenotypes in general among women than among men. Odds ratio analysis indicated that individuals with this polymorphic variant have an approximately 2-fold risk of developing these cancers. GSTM1 phenotype distribution depends on age, smoking habit and tumour pathology. A group of MM patients with dysplastic naevi was also studied.lld:pubmed
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pubmed-article:7640212pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:7640212pubmed:articleTitlePhenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma. MMM group. Multidisciplinary Malignant Melanoma Group.lld:pubmed
pubmed-article:7640212pubmed:affiliationInstitute de Salut Pública, Universitat de Barcelona, Spain.lld:pubmed
pubmed-article:7640212pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7640212pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:7640212pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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