Does Occupational Exposure to Solvents and Pesticides in Association with Glutathione S-Transferase A1, M1, P1, and T1 Polymorphisms Increase the Risk of Bladder Cancer? The Belgrade Case-Control Study
Objective We investigated the role of the glutathione S-transferase A1, M1, P1 and T1 gene polymorphisms and potential effect modification by occupational exposure to different chemicals in Serbian bladder cancer male patients. Patients and Methods A hospital-based case-control study of bladder cancer in men comprised 143 histologically confirmed cases and 114 age-matched male controls. Deletion polymorphism of glutathione S-transferase M1 and T1 was identified by polymerase chain reaction method. Single nucleotide polymorphism of glutathione S-transferase A1 and P1 was identified by restriction fragment length polymorphism method. As a measure of effect size, odds ratio (OR) with corresponding 95% confidence interval (95%CI) was calculated. Results The glutathione S-transferase A1, T1 and P1 genotypes did not contribute independently toward the risk of bladder cancer, while the glutathione S-transferase M1-null genotype was overrepresented among cases (OR = 2.1, 95% CI = 1.1–4.2, p = 0.032). The most pronounced effect regarding occupational exposure to solvents and glutathione S-transferase genotype on bladder cancer risk was observed for the low activity glutathione S-transferase A1 genotype (OR = 9.2, 95% CI = 2.4–34.7, p = 0.001). The glutathione S-transferase M1-null genotype also enhanced the risk of bladder cancer among subjects exposed to solvents (OR = 6,5, 95% CI = 2.1–19.7, p = 0.001). The risk of bladder cancer development was 5.3–fold elevated among glutathione S-transferase T1-active patients exposed to solvents in comparison with glutathione S-transferase T1-active unexposed patients (95% CI = 1.9–15.1, p = 0.002). Moreover, men with glutathione S-transferase T1-active genotype exposed to pesticides exhibited 4.5 times higher risk in comparison with unexposed glutathione S-transferase T1-active subjects (95% CI = 0.9–22.5, p = 0.067). Conclusion Null or low-activity genotypes of the glutathione S-transferase A1, T1, and P1 did not contribute independently towards the risk of bladder cancer in males. However, in association with occupational exposure, low activity glutathione S-transferase A1 and glutathione S-transferase M1-null as well as glutathione S-transferase T1-active genotypes increase individual susceptibility to bladder cancer.
References
[1]
Kim JJ (2012) Recent advances in treatment of advanced urothelial carcinoma. Curr Urol Rep 13: 147–52. doi: 10.1007/s11934-012-0238-0
[2]
Siegel R, Naishadham D, Jemal A (2012) Cancer statistics. CA Cancer J Clin 62: 10–29. doi: 10.3322/caac.20138
[3]
American Cancer Society (2012) Bladder Cancer 2012. American Cancer Society, Atlanta, USA.
[4]
Olfert SM, Felknor SA, Delclos GL (2006) An updated review of the literature: risk factors for bladder cancer with focus on occupational exposures. South Med J 99: 1256–63. doi: 10.1097/01.smj.0000247266.10393.72
[5]
Clapp RW, Howe G, Lefevre MJ (2005) Environmental an Occupational Causes of Cancer, A Review of Recent Scientific Literature. Lowell Center for Sustainable Production. Lowe Mass, USA
[6]
International Agency for Research on Cancer (2010) Painting, fire- fighting, and shiftwork. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. pp. 43–394.
[7]
Schulte PA, Ringen K, Hemstreet GP, Ward E (1987) Occupational cancer of the urinary tract. Occup Med 2: 85–107.
[8]
International Agency for Research on Cancer (2010) Some aromatic amines, organic dyes, and related exposures. IARC Mono-graphs on the Evaluation of Carcinogenic Risks to Humans. pp. 1–692.
[9]
International Agency for Research on Cancer (2010) Some non-heterocyclic polycyclic aromatic hydrocarbons and some related compounds. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. pp. 754–759.
[10]
Pukkala E, Martinsen JI, Lynge E, Gunnarsdottir HK, Sparén P, et al. (2009) Occupation and cancer follow-up of 15 million people in five Nordic countries. Acta Oncologica 48: 646–790. doi: 10.1080/02841860902913546
[11]
Simic T, Mimic-Oka J, Savic-Radojevic A, Opacic M, Pljesa M, et al. (2005) Glutathione S-transferase T1-1 activity upregulated in transitional cell carcinoma of urinary bladder. Urology 65: 1035–40. doi: 10.1016/j.urology.2005.01.005
[12]
Di Pietro G, Magno LA, Rios-Santos F (2010) Glutathione S-transferases: an overview in cancer research. Expert Opin Drug Metab Toxicol 6: 153–70. doi: 10.1517/17425250903427980
[13]
Eaton DL, Bammler TK (1999) Concise review of the glutathione S-transferases and their significance to toxicology. Toxicol Sci 49: 156–64. doi: 10.1093/toxsci/49.2.156
[14]
Landi S (2000) Mammalian class θ GST and differential susceptibility to carcinogens: a review. Mutat Res 463: 247–83. doi: 10.1016/s1383-5742(00)00050-8
[15]
Watson MA, Stewart RK, Smith GB Massey TE, Bell DA (1998) Human glutathione S-transferase P1 polymorphisms: relationship to lung tissue enzyme activity and population frequency distribution. Carcinogenesis 19: 275–80. doi: 10.1093/carcin/19.2.275
[16]
Coles FB, Kadlubar FF (2005) Human alpha class glutathione S-transferases: genetic polymorphism, expression, and susceptibility to disease. In: Helmut S, Lester P, editors. Glutathione Transferases and Gamma-Glutamyl Transpeptidases, Methods Enzymology. London: Elsevier Academic Press. pp 9–42.
[17]
Abdel-Rahman SZ, El-Zein RA, Anwar WA, Au WW (1996) A multiplex PCR procedure for polymorphic analysis of GSTM1 and GSTT1 genes in population studies. Cancer Lett 107: 229–33. doi: 10.1016/0304-3835(96)04832-x
[18]
Harries LW, Stubbins MJ, Forman D, Howard GC, Wolf CR (1997) Identification of genetic polymorphisms at the glutathione S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer. Carcinogenesis 18: 641–44. doi: 10.1093/carcin/18.4.641
[19]
Hirvonen A (2005) Gene–environment interaction and biological monitoring of occupational exposures. Toxicol Appl Pharmacol 207: 329–335. doi: 10.1016/j.taap.2004.11.030
[20]
Miller DP, Asomaning K, Liu G, Wain JC, Lynch TJ, et al. (2006) An association between glutathione S-transferase P1 gene polymorphism and younger age at onset of lung carcinoma. Cancer 107: 1570–7. doi: 10.1002/cncr.22124
[21]
Heuser VD, Erdtmann B, Kvitko K, Rohr P, da Silva J (2007) Evaluation of genetic damage in Brazilian footwear-workers: Biomarkers of exposure, effect, and susceptibility. Toxicology 232: 235–47. doi: 10.1016/j.tox.2007.01.011
[22]
Lynge E, Anttila A, Hemminki A (1997) Organic solvents and cancer. Cancer Causes Control 8: 406–19. doi: 10.1023/a:1018461406120
[23]
Risch HA, Burch JD, Miller AB, Hill GB, Steele R, et al. (1988) Occupational factors and the incidence of cancer of the bladder in Canada. Br Industr Med 45: 361–367. doi: 10.1136/oem.45.6.361
[24]
Bonassi S, Merlo F, Pearce N, Puntoni R (1989) Bladder cancer an occupational exposure to polycyc aromatic hydrocarbons. Int Cancer 44: 648–651. doi: 10.1002/ijc.2910440415
[25]
La Vecchia C, Negri E, D'Avanzo B, Franceschi S (1990) Occupation and the risk of bladder cancer. Int J Epidemiol 19: 264–8. doi: 10.1093/ije/19.2.264
[26]
Cordier S, Clavel J, Limasset JC, Boccon-Gibod L, Le Moual N, et al. (1993) Occupational risks of bladder cancer in France: A multicentre case-control study. Int J Epidemiol 22: 402–11. doi: 10.1093/ije/22.3.403
[27]
Lohi J, Kyyr?nen P, Kauppinen T, Kujala V, Pukkala E (2008) Occupational exposure to solvents and gasoline and risk of cancers in the urinary tract among Finnish workers. Am J Ind Med 51: 668–72. doi: 10.1002/ajim.20606
[28]
Honaker MT, Acchione M, Zhang W, Mannervik B, Atkins WM (2013) Enzymatic detoxication, conformational selection, and the role of molten globule active sites. J Biol Chem 288: 18599–611. doi: 10.1074/jbc.m112.445767
[29]
Hayes JD, Strange RC (2000) Glutathione S-transferase polymorphisms and their biological consequences. Pharmacology 61: 154–66. doi: 10.1159/000028396
[30]
Weber LW, Boll M, Stampfl A (2003) Hepatotoxicity and mechanism of action of haloalkanes: carbon tetrachloride as a toxicological model. Crit Rev Toxicol 33: 105–36. doi: 10.1080/713611034
[31]
Savic-Radojevic A, Mimic-Oka J, Pljesa-Ercegovac M, Opacic M, Dragicevic D, et al. (2007) Glutathione S-transferase-P1 expression correlates with increased antioxidant capacity in transitional cell carcinoma of the urinary bladder. Eur Urol 52: 470–7. doi: 10.1016/j.eururo.2007.01.046
[32]
Rossi AM, Guarnieri C, Rovesti S, Gobba F, Ghittori S, et al. (1999) Genetic polymorphisms influence variability in benzene metabolism in humans. Pharmacogenetics 9: 445–51.
[33]
Guengerich P (2005) Activation of alkyl halides by glutathione transferases. In: Helmut S, Lester P, editors. Glutathione Transferases and Gamma-Glutamyl Transpeptidases, Methods Enzymology. London: Elsevier Academic Press.pp 9–42.
[34]
Ruder AM, Yiin JH, Waters MA, Carreón T, Hein MJ, et al. (2013) The Upper Midwest Health Study: gliomas and occupational exposure to chlorinated solvents. Occup Environ Med 70: 73–80. doi: 10.1136/oemed-2011-100588
[35]
Buzio L, De Palma G, Mozzoni P, Tondel M, Buzio C, et al. (2003) Glutathione S-transferases M1-1 and T1-1 as risk modifiers for renal cell cancer associated with occupational exposure to chemicals. Occup Environ Med 60: 789–93. doi: 10.1136/oem.60.10.789
[36]
Moore LE, Boffetta P, Karami S, Brennan P, Stewart PS, et al. (2010) Occupational trichloroethylene exposure and renal carcinoma risk: evidence of genetic susceptibility by reductive metabolism gene variants. Cancer Res 70: 6527–36. doi: 10.1158/0008-5472.can-09-4167
[37]
Simic T, Savic-Radojevic A, Pljesa-Ercegovac M, Matic M, Mimic-Oka J (2009) Glutathione S-transferases in kidney and urinary bladder tumors. Nat Rev Urol 6: 281–9. doi: 10.1038/nrurol.2009.49
[38]
Thier R, Golka K, Brüning T, Ko Y, Bolt HM (2002) Genetic susceptibility to environmental toxicants: the interface between human and experimental studies in the development of new toxicological concepts. Toxicol Lett 127: 321–7. doi: 10.1016/s0378-4274(01)00515-x
[39]
Band PR, Le ND, MacArthur AC, Fang R, Gallagher RP (2005) Identification of occupational cancer risks in British Columbia: a population-based case-control study of 1129 cases of bladder cancer. J Occup Environ Med 47: 854–8.
[40]
Zahm SH (1997) Mortality study of pesticide applicators and other employees of a lawn care service company. J Occup Environ Med 39: 1055–67. doi: 10.1097/00043764-199711000-00006
[41]
Viel F-F, Challier B (1995) Bladder cancer among French farmers: does exposure to pesticides in vineyards play a part? Occup Environ Med 52: 587–92. doi: 10.1136/oem.52.9.587
[42]
Falck GC, Hirvonen A, Scarpato R, Saarikoski ST, Migliore L, et al. (1999) Micronuclei in blood lymphocytes and genetic polymorphism for GSTM1, GSTT1 and NAT2 in pesticide-exposed greenhouse workers. Mutat Res 441: 225–37. doi: 10.1016/s1383-5718(99)00051-0
[43]
Scarpato R, Migliore L, Hirvonen A, Falck G, Norppa H (1996) Cytogenetic monitoring of occupational exposure to pesticides: characterization of GSTM1, GSTT1, and NAT2 genotypes. Environ Mol Mutagen 27: 263–9. doi: 10.1002/(sici)1098-2280(1996)27:4<263::aid-em3>3.0.co;2-e
[44]
Karami S, Boffetta P, Rothman N, Hung RJ, Stewart T, et al. (2008) Renal cell carcinoma, occupational pesticide exposure and modification by glutathione S transferase polymorphisms. Carcinogenesis 29: 1567–71. doi: 10.1093/carcin/bgn153