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Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study
BACKGROUND: Nasopharyngeal carcinoma (NPC) is a rare tumor in most parts of the world but occurs at relatively high frequency among people of Chinese descent. The cytochrome P450 2E1 enzyme (CYP2E1) is responsible for the metabolic activation of nitrosamines, and has been shown to be a susceptibilit...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2001
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32196/ https://www.ncbi.nlm.nih.gov/pubmed/11389775 http://dx.doi.org/10.1186/1471-2407-1-4 |
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author | Kongruttanachok, Narisorn Sukdikul, Sairoong Setavarin, Surachai Kerekhjanarong, Verachai Supiyaphun, Pakpoom Voravud, Narin Poovorawan, Yong Mutirangura, Apiwat |
author_facet | Kongruttanachok, Narisorn Sukdikul, Sairoong Setavarin, Surachai Kerekhjanarong, Verachai Supiyaphun, Pakpoom Voravud, Narin Poovorawan, Yong Mutirangura, Apiwat |
author_sort | Kongruttanachok, Narisorn |
collection | PubMed |
description | BACKGROUND: Nasopharyngeal carcinoma (NPC) is a rare tumor in most parts of the world but occurs at relatively high frequency among people of Chinese descent. The cytochrome P450 2E1 enzyme (CYP2E1) is responsible for the metabolic activation of nitrosamines, and has been shown to be a susceptibility gene for NPC development in Taiwan [RR = 2.6; 95%CI = 1.2-5.7]. Since there has been only one report of this link, it was decided to investigate the susceptibility of CYP2E1 to NPC development in other populations. Therefore, the correlation between the RsaI polymorphism of this gene and NPC was studied in-patients including Thai and Chinese in Thailand. The present study comprised 217 cases diagnosed with NPC and 297 healthy controls. RESULTS: Similar to the result found in Taiwanese, a homozygous uncut genotype demonstrated a higher relative risk both when all cases were analyzed [RR = 2.19; 95%CI = 0.62-8.68] or individual racial groups, Thai [RR = 1.51; 95%CI = 0.08-90.06] or Chinese [RR = 1.99; 95%CI = 0.39-10.87]. The ethnicity-adjusted odds ratio is 2.39 with 95%CI, 0.72-7.89. CONCLUSIONS: Though our finding was not statistically significant due to the moderate sample size of the study, similarity to the study in Taiwan with only a slight loss in precision was demonstrated. The higher RR found for the same genotype in distinct populations confirmed that CYP2E1 is one of several NPC susceptibility genes and that the RsaI minus variant is one mutation that affects phenotype. |
format | Text |
id | pubmed-32196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-321962001-06-05 Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study Kongruttanachok, Narisorn Sukdikul, Sairoong Setavarin, Surachai Kerekhjanarong, Verachai Supiyaphun, Pakpoom Voravud, Narin Poovorawan, Yong Mutirangura, Apiwat BMC Cancer Research Article BACKGROUND: Nasopharyngeal carcinoma (NPC) is a rare tumor in most parts of the world but occurs at relatively high frequency among people of Chinese descent. The cytochrome P450 2E1 enzyme (CYP2E1) is responsible for the metabolic activation of nitrosamines, and has been shown to be a susceptibility gene for NPC development in Taiwan [RR = 2.6; 95%CI = 1.2-5.7]. Since there has been only one report of this link, it was decided to investigate the susceptibility of CYP2E1 to NPC development in other populations. Therefore, the correlation between the RsaI polymorphism of this gene and NPC was studied in-patients including Thai and Chinese in Thailand. The present study comprised 217 cases diagnosed with NPC and 297 healthy controls. RESULTS: Similar to the result found in Taiwanese, a homozygous uncut genotype demonstrated a higher relative risk both when all cases were analyzed [RR = 2.19; 95%CI = 0.62-8.68] or individual racial groups, Thai [RR = 1.51; 95%CI = 0.08-90.06] or Chinese [RR = 1.99; 95%CI = 0.39-10.87]. The ethnicity-adjusted odds ratio is 2.39 with 95%CI, 0.72-7.89. CONCLUSIONS: Though our finding was not statistically significant due to the moderate sample size of the study, similarity to the study in Taiwan with only a slight loss in precision was demonstrated. The higher RR found for the same genotype in distinct populations confirmed that CYP2E1 is one of several NPC susceptibility genes and that the RsaI minus variant is one mutation that affects phenotype. BioMed Central 2001-05-25 /pmc/articles/PMC32196/ /pubmed/11389775 http://dx.doi.org/10.1186/1471-2407-1-4 Text en Copyright © 2001 Kongruttanachok et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Kongruttanachok, Narisorn Sukdikul, Sairoong Setavarin, Surachai Kerekhjanarong, Verachai Supiyaphun, Pakpoom Voravud, Narin Poovorawan, Yong Mutirangura, Apiwat Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title | Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title_full | Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title_fullStr | Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title_full_unstemmed | Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title_short | Cytochrome P450 2E1 polymorphism and nasopharyngeal carcinoma development in Thailand: a correlative study |
title_sort | cytochrome p450 2e1 polymorphism and nasopharyngeal carcinoma development in thailand: a correlative study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32196/ https://www.ncbi.nlm.nih.gov/pubmed/11389775 http://dx.doi.org/10.1186/1471-2407-1-4 |
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