Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cccn.2005.06.021
Title: Rapid determination of common mutations in glutathione S-transferase gene by PCR-based methods in healthy Chinese
Authors: Zhong, S.-L.
Zhou, S. 
Chen, X.
Huang, M.
Keywords: Glutathione S-transferase
Han Chinese
Mutation
PCR
Uygur Chinese
Issue Date: Feb-2006
Citation: Zhong, S.-L., Zhou, S., Chen, X., Huang, M. (2006-02). Rapid determination of common mutations in glutathione S-transferase gene by PCR-based methods in healthy Chinese. Clinica Chimica Acta 364 (1-2) : 205-208. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cccn.2005.06.021
Abstract: Background: The glutathione S-transferase (GST) superfamily comprises multiple isozymes with compelling evidence of functional polymorphisms in various ethnic groups. All these mutations, in particular those in class μ, π and θ GST, are likely to contribute to interindividual differences in responses to xenobiotics including response to chemotherapy and associated with altered disease. The frequency of common GST mutations in Uygur Chinese is unknown. We investigated the common mutations of GSTM1, GSTT1, and GSTP1 in Uygur (N = 154) Chinese and compare with Han Chinese (N = 196). Method: GSTM1 and GSTT1 polymorphisms were analyzed by multiplexed PCR, and GSTP1 polymorphism was detected by PCR-based restriction fragment length polymorphism (RFLP) analysis. Results: GSTM1 null genotype was found in 53.2% Uygur Chinese, which was close to that in Han Chinese (56.1%) (P = 0.592). A significantly lower frequency (P < 0.05) of GSTT1 null genotype in Uygur Chinese (26.6%) was observed compared with Han Chinese (50.0%). Uygur Chinese exhibited a GSTP1 genotype distribution of 51.3% I/I, 40.2% I/V and 8.4% V/V, which was different from that in Han Chinese (60.7% I/I, 35.2% I/V and 4.1% V/V). Conclusions: There is marked ethnic difference in the frequency of common GSTT1 and GSTP1 mutation, but not GSTM1 mutation, between Uygur and Han Chinese. © 2005 Elsevier B.V. All rights reserved.
Source Title: Clinica Chimica Acta
URI: http://scholarbank.nus.edu.sg/handle/10635/106289
ISSN: 00098981
DOI: 10.1016/j.cccn.2005.06.021
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