Genetic polymorphisms of glutathione S-transferase mu1 and theta1 in patients with acquired aplastic anemia: A Brazilian experience

0Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

The causes of acquired aplastic anemia (AAA) include immunologic mechanisms and oxidative DNA damage. Glutathione S-Transferase (GST) plays an important role in detoxification. In humans, GST genes encode four main clones: alpha (A), mu (M), pi (P) and theta (T). Among GST genes, GST M1 and T1 have null genotypes that result in a lack of activity. The aim of this study was to investigate polymorphisms of the GSTM1 and GSTT1 enzyme in Brazilian patients with AAA. The null allele of GSTM1 was observed in 3 (16.6%) patients and the GSTT1 null genotype was observed in only one (5.5%) patient. This study did not find any association between genetic polymorphisms of the GSTM1/GSTT1 detoxifying enzymes and the pathogenesis of AAA.

Cite

CITATION STYLE

APA

Vicari, P., Duch, C. R., Shimmoto, M. M. A., Noguti, M. A. E., & Figueiredo, M. S. (2007). Genetic polymorphisms of glutathione S-transferase mu1 and theta1 in patients with acquired aplastic anemia: A Brazilian experience. Revista Brasileira de Hematologia e Hemoterapia, 29(4), 344–345. https://doi.org/10.1590/S1516-84842007000400005

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free