Interaction of glutathione-s-transferase genotypes with environmental risk factors in determining susceptibility to head and neck cancer and treatment response and survival outcome

被引:11
|
作者
Katiyar, Tridiv [1 ,2 ]
Yadav, Vinay [1 ]
Maurya, Shailendra S. [3 ]
Ruwali, Munindra [4 ]
Singh, Madhu [5 ]
Hasan, Feza [1 ,2 ]
Pandey, Rahul [6 ,7 ]
Mehrotra, Divya [6 ,7 ]
Singh, Sudhir [6 ,7 ]
Mishra, Shambhavi [8 ]
Hadi, Rahat [9 ]
Bhatt, Madan L. B. [6 ,7 ]
Parmar, Devendra [1 ]
机构
[1] IITR, CSIR, Syst Toxicol & Hlth Risk Assessment Grp, 31 MG Marg,POB 80, Lucknow 226001, Uttar Pradesh, India
[2] Babu Banarsi Das Univ, Lucknow, Uttar Pradesh, India
[3] Washington Univ, Dept Pediat, Div Hematol Oncol Dev Biol & Genet, St Louis, MO 63130 USA
[4] Amity Univ, Amity Inst Biotechnol, Gurgaon, Haryana, India
[5] Balrampur Hosp, Lucknow, Uttar Pradesh, India
[6] King Georges Med Univ, Dept Oral & Maxillofacial Surg, Lucknow, Uttar Pradesh, India
[7] King Georges Med Univ, Dept Radiotherapy, Lucknow, Uttar Pradesh, India
[8] Univ Lucknow, Dept Stat, Lucknow, Uttar Pradesh, India
[9] Dr Ram Manohar Lohia Inst Med Sci, Dept Radiat Oncol, Lucknow, Uttar Pradesh, India
关键词
GSTs; HNSCC; interaction; polymorphism; risk; tobacco; DRUG-METABOLIZING-ENZYMES; GSTT1 GENE LOCI; LUNG-CANCER; ORAL-CANCER; POOLED ANALYSIS; GSTP1; POLYMORPHISM; GSTM1; CYP1A1; TOBACCO; ASSOCIATION;
D O I
10.1002/em.22362
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present case-control study aimed to investigate the role of interaction of glutathione-s-transferase (GST) genotypes with environmental risk factors in determining susceptibility to head and neck squamous cell carcinoma (HNSCC) involving 1,250 cases and equal number of healthy controls. An increase in the risk of HNSCC and its subsites (larynx, pharynx, and oral cavity) was observed among the cases with null genotypes of GSTM1 (odds ratio [OR] = 1.87) or GSTT1 (OR = 1.39) while reduced risk (OR = 0.81) was observed the cases with variant genotype of GSTP1. Tobacco use in the form of smoking or chewing interacted multiplicatively with GSTM1 or GSTT1 to increase the risk several folds (3-10 folds) in HNSCC and its subsites. Alcohol use also increased the risk (2-3 folds) to HNSCC and its subsites in cases with null or variant genotypes of GSTs, though this risk was of lesser magnitude when compared to the tobacco users. A synergistic effect of both, tobacco smoking and alcohol drinking, led to several folds (25-folds) increased risk to HNSCC among the cases with null genotype of GSTM1 and GSTT1 when compared to nonsmokers and nondrinkers with wild genotype of GSTM1 and GSTT1 in controls. Furthermore, cases with variant genotypes of GSTP1 (Val/Val) showed superior treatment response with improved survival rate and lower risk of death when compared to the patients with wild type genotype (Ile/Ile). The data suggest that though polymorphism in GSTs may be a modest risk factor for determining HNSCC risk, gene-environment interactions significantly modify the susceptibility to HNSCC by several folds.
引用
收藏
页码:574 / 584
页数:11
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