How to Cite
Cardona Rivas, D., Castaño Molina, E., & Marín Marmolejo, J. C. (2007). Gastric cancer, tobacco usage, alcohol consumption, socioeconomic stratification and polymorphism in codon 72 of gene p53 in a population of Manizales. Biosalud, 6, 33–44. Retrieved from https://revistasojs.ucaldas.edu.co/index.php/biosalud/article/view/5843

Authors

Dora Cardona Rivas
Universidad Autónoma de Manizales
eduardo.castano@ucaldas.edu.co
Eduardo Castaño Molina
Universidad de Caldas. Manizales
eduardo.castano@ucaldas.edu.co
Juan Carlos Marín Marmolejo
Universidad de Caldas. Manizales
eduardo.castano@ucaldas.edu.co

Abstract

The polymorphic variants of codon 72 of the tumor suppressor gene P53 (TP53) have been related with increased susceptibility to certain types of neoplasms, and for this reason we explored the possible relationship of these polymorphisms and interaction with demographic factors such as tobacco usage, alcohol consumption and socioeconomic stratification, with gastric cancer (GC) in a high risk Colombian population. Gastric cancer cases identified at the Hospital de Caldas in the city of Manizales, Colombia were collected for 18 months. Seventy-five patients were initially identified, from which 65 complied the inclusion criteria for the study. An EDTA peripheral blood sample was obtained from every participant. DNA was extracted with the salting out method and the P53 genotypification was determined for RFLP-PCR. No significant differences in the frequencies for variants of codon 72 of the tumor suppressor gene (TP53) between patients and controls were found (Arg/Arg=47.7; Arg/ Pro=38.5; Pro/Pro=13.8%; and Arg/Arg=49.2; Arg/Pro=41.5 and Pro/Pro=9.2, espectively), nor when the interaction with tobacco usage was estimated. These results did not identify an association between the polymorphism of codon 72 of the tumor suppressor gene P53, nor any interaction of these polymorphic variants, with tobacco usage, alcohol consumption and the risk of GC in this population. A higher effect is seen from tobacco usage and socioeconomic stratification on the GC risk.

Archie V, Kauh J, Jones DV, Cruz V, Karpeh MS, Thomas CR. Gastric cancer: Standards for the 21st century. Crit Rev Oncol Hematol 2006; 57:123-31.

Jemal A, Thomas A, Murray T, Thun M. Cancer statistics, 2002. CA Cancer J Clin 2006; 52:23-47.

Murillo MR, Piñeros PM, Hernández SG. Atlas de Mortalidad por Cáncer en Colombia 2003. Imprenta Nacional de Colombia; 2003.

Hesketh, R. The Oncogene and Tumour Suppressor gen. 2a. edic. Academic Press- London. Great Britain; 1997.

Shepherd T, Tolbert D, Benedetti J, MacDonald J, Stermmermann G, Weist J, et al. Alterations in exon 4 of the p53 gene in gastric carcinoma. Gastroenterology 2000; 118:1039-44.

Shu KX, Li B, Wu LX. The p53 network: p53 and its downstream genes. Colloids Surf B Biointerfaces 2007; 55:10-18.

Fan R, Wu MT, Miller D, Wain JC, Kelsey KT, Wiencke JK, et al. The p53 codon 72 polymorphism and lung cancer risk. Cancer Epidemiol Biomarkers Prev 2000; 10:1037-42.

Torres MM, Acosta CP, Sicard DM, Groot, de Restrepo H. Genetic susceptibility and risk of gastric cancer in a human population of Cauca, Colombia. Biomédica 2004; 24:153-62.

Lindblad M, Rodriguez LA, Lagergren J. Body mass, tobacco and alcohol and risk of esophageal, gastric cardia, and gastric non-cardia adenocarcinoma among men and women in a nested case-control study. Cancer Causes Control 2005; 3:285-94.

Setiawan VW, Zhang ZF, Yu GP, Li YL, Lu ML, Tsai CJ, et al. GSTT1 and GSTM1 Null Genotypes and the risk of gastric cancer: a case-control study in a Chinese population. Cancer Epidemiol Biomarkers Prev. 2000; 9:73-80.

Blin N, Stafford DW. A general method for isolation of high molecular weight DNA from eukaryotes. Nuclei Acids Res. 1976; 3:2303-08.

Ye W, Ekstrom AM, Hansson LE, Bergstrom R, Nyren O. Tobacco, alcohol and the risk of gastric cancer by sub-site and histologic type. Int J. Cancer 1999; 83:223-229.

Plummer M, Franceschi S, Muñoz N. Epidemiolgy of gastric cancer. IARC Sci Publ. 2004; 157:311-26.

Peláez A, Ramírez JG, Ruíz A. Características y prevalencia de neoplasias malignas del tracto gastrointestinal en el departamento de Antioquia, Segundo semestre de 1996. CES MEDICINA 1998; 12:37-43.

Newton JL. Changes in upper gastrointestinal physiology with age. Mech Ageing Dev. 2004; 125:867-870.

Suzuki K, Suzuki I, Leodolter A, Alonso S, Horiuchi S, Yamashita K, et al. Global DNA demethylation in gastrointestinal cancer is age dependent and precedes genomic damage. Cancer Cell 2006; 9:199-207.

Marchand LL, Wilkinson GR, Wilkens LR. Genetic and dietary predictors of CYP2E1 activity: a phenoyping study in Hawaii Japanese using chlorzoxazone. Cancer Epidemiol Biomarkers Prev. 1999; 8:495-500.

Kim HS, Kwack SJ, Lee BM. Alteration of cytochrome p-450 and glutathione s-transferase activity in normal and malignant human stomach. Journal of toxicology and environmental health, part a. 2005; 68:1611-20.

Maguire A, Porta M, Sanz JM, Ruano I, Malats N, Piñol JL. Sex as a pronostic factor in gastric cancer. European Journal of Cancer 1996; 32A:1303-09.

Tredaniel J, Boffetta P, Buiatti E, Saracci R, Hirsch A. Tobacco smoking and gastric cancer: review and meta analysis. Int J Cancer 1997; 72:565-73.

Katoh T, Nagata N, Kuroda Y, Itoh H, Kawahara A, Kuroki N, et al. Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) genetic polymorphism and susceptibility to gastric and colorectal adenocarcinoma. Carcinogenesis 1996; 17:1855-59.

Shin VY, Cho CH. Nicotine and gastric cancer. Alcohol 2005; 35:259-64.

González CA, Pera G, Agudo A, Palli D, Krogh V, Vineis P, et al. Smoking and the risk of gastric cancer in the European Prospective Investigation Into Cancer and Nutrition (EPIC). Int J Cancer 2003; 107:629-34.

Correa P. A human model of gastric carcinogenesis. Cancer Res 1988; 48:3554-60.

Mirvish SS. Role of N-nitroso compounds (NOC) and N-nitrosation in etiology of gastric, esophageal, nasopharyngeal and bladder cancer and contribution to cancer of known exposures to NOC. Cancer Lett 1995; 93:17-48.

Schoket B, Phillips DH, Kostic S, Vincze I. Smoking-associated bulky DNA adducts in bronchial tissue related to CYP1A1 MspI and GSTM1 genotypes in lung patients. Carcinogenesis 1998; 19:841-46.

Iwata F, Zhang XY, Leung FW. Aggravation of gastric mucosal lesions in rat stomach by tobacco cigarette smoke. Digest Dis Sci. 1995; 40:1118-24.

Shin VY, Wang HY, Liu ES, Koo MN, Cho CH. Differential effects of cigarette smoke extracts on cell proliferation in gastric and colon cells. Cancer Invest. 2003; 2:200-07.

Salam SA, Abdel SZ, Sierra CH, Hamada FA, Au WW. Role of polymorphic GSTM1 and GSTT1 genotypes on NNK-induced genotoxicity. Pharmacogenetics 1999; 9:735-43.

Kneller RW, You WC, Chang YS, Liu WD, Zhang L, Zhao L, et al. Cigarette smoking and other risk factors for progression of precancerous stomach lesions. J Nat Cancer Inst. 1992; 84:1261-66.

Sanz JM, Ruiz JM, Rodríguez L, Alfaro J, Almajano C, Cuevas M, et al. Importancia de la clasificación de Laurén del cáncer gástrico. Revisión de una serie de 295 casos. Patología 1989; 22:156-61.

Evans GW, Kantrowitz E. Socioeconomic status and health: the potential role of environmental risk exposure. Annu Rev Public Health 2002; 23:303-31.

Zhou Y, Li N, Zhuang W, Liu GJ, Wu TX, Yao X, et al. P53 codon 72 polymorphism and gastric cancer: A meta-analysis of the literature. Int J Cancer. 2007 Jun 1; [Epub ahead of print].

Downloads

Download data is not yet available.
Sistema OJS - Metabiblioteca |