Research Papers:

Cross-sectional associations between genetic polymorphisms in metabolic enzymes and longer leukocyte telomere length induced by omethoate

Xiaoran Duan, Yongli Yang, Sihua Wang, Xiaolei Feng, Tuanwei Wang, Pengpeng Wang, Suxiang Liu, Lei Li, Guoyu Li, Wu Yao, Liuxin Cui and Wei Wang _

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Oncotarget. 2017; 8:80638-80644. https://doi.org/10.18632/oncotarget.20971

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Xiaoran Duan1, Yongli Yang2, Sihua Wang3, Xiaolei Feng1, Tuanwei Wang1, Pengpeng Wang1, Suxiang Liu4, Lei Li4, Guoyu Li4, Wu Yao1, Liuxin Cui1 and Wei Wang1

1Department of Occupational and Environmental Health, College of Public Health, Zhengzhou University, Zhengzhou, China

2Department of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou, China

3Department of Occupational Health, Henan Institute for Occupational Medicine, Zhengzhou, China

4Clinical Department, Zhengzhou Institute of Occupational Health, Zhengzhou, China

Correspondence to:

Wei Wang, email: ww375@126.com

Yongli Yang, email: ylyang377@126.com

Keywords: omethoate, telomere, polymorphism, metabolic enzymes

Received: June 27, 2017     Accepted: August 29, 2017     Published: September 18, 2017


Purpose: This study aimed to explore the effects of genetic polymorphisms in metabolic enzymes on relative telomere length changes and explore the mechanism of canceration induced by omethoate.

Materials and Methods: 180 long-term omethoate-exposed workers and 115 healthy controls were recruited. Real-time PCR method was applied to determine the relative telomere length in peripheral blood leukocytes DNA, and Six polymorphic loci of GSTT1(+/−), GSTM1(+/−), GSTP1 rs1695, CYP2E1 rs6413432, CYP2E1 rs3813867 and PON2 rs12026 were detected by polymerase chain reaction and restriction fragment length polymorphism method; Multiple linear regression was conducted to explore the effects of omethoate exposure and genetic polymorphisms on the telomere length.

Results: The relative telomere lengths in the control group (0.94 [0.76, 1.32]) were significantly shorter than that in the exposure group (1.50 [1.11, 2.57]) (Z = 7.910, P < 0.001). Univariate analysis showed that the relative telomere lengths of the GSTM1-deletion individuals were significantly longer than that of the non - deletion genotype in the control group (Z = 2.911, P = 0.004), and the relative telomere lengths of GSTP1 rs1695 polymorphism locus (GG+AG) genotype individuals were longer than that of AA genotype in the exposure group. The difference was statistically significant (Z = 2.262, P = 0.024). Multivariate analysis found that pesticide-exposure (b = 0.524, P < 0.001) and GSTM1 polymorphism (b = −0.136, P = 0.029) had an impact on telomere length.

Conclusions: The relative telomere lengths of omethoate-exposure workers were longer than that in the control population. Also GSTM1 genetic polymorphism may influence the changes of the telomere length induced by omethoate.

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