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Association of −330 interleukin-2 gene polymorphism with oral cancer

BACKGROUND & OBJECTIVES: Cytokines play an important role in the development of cancer. Several single-nucleotide polymorphisms (SNPs) of cytokine genes have been reported to be associated with the development and severity of inflammatory diseases and cancer predisposition. This study was undert...

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Autores principales: Singh, Prithvi Kumar, Kumar, Vijay, Ahmad, Mohammad Kaleem, Gupta, Rajni, Mahdi, Abbas Ali, Jain, Amita, Bogra, Jaishri, Chandra, Girish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926344/
https://www.ncbi.nlm.nih.gov/pubmed/29664031
http://dx.doi.org/10.4103/ijmr.IJMR_1949_15
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author Singh, Prithvi Kumar
Kumar, Vijay
Ahmad, Mohammad Kaleem
Gupta, Rajni
Mahdi, Abbas Ali
Jain, Amita
Bogra, Jaishri
Chandra, Girish
author_facet Singh, Prithvi Kumar
Kumar, Vijay
Ahmad, Mohammad Kaleem
Gupta, Rajni
Mahdi, Abbas Ali
Jain, Amita
Bogra, Jaishri
Chandra, Girish
author_sort Singh, Prithvi Kumar
collection PubMed
description BACKGROUND & OBJECTIVES: Cytokines play an important role in the development of cancer. Several single-nucleotide polymorphisms (SNPs) of cytokine genes have been reported to be associated with the development and severity of inflammatory diseases and cancer predisposition. This study was undertaken to evaluate a possible association of interleukin 2 (IL-2) (− 330A>C) gene polymorphisms with the susceptibility to oral cancer. METHODS: The SNP in IL-2 (−330A>C) gene was genotyped in 300 oral cancer patients and in similar number of healthy volunteers by polymerase chain reaction (PCR)-restriction fragment length polymorphism and the association of the gene with the disease was evaluated. RESULTS: IL-2 (−330A>C) gene polymorphism was significantly associated with oral cancer whereas it was neither associated with clinicopathological status nor with cancer pain. The AC heterozygous genotype was significantly associated with oral cancer patients as compared to controls [odds ratio (OR): 3.0; confidence interval (CI): 2.14-4.20; P<0.001]. The C allele frequency was also significantly associated with oral cancer (OR: 1.80; CI: 1.39-2.33; P<0.001). IL-2 (−330A>C) gene polymorphism was also associated with oral cancer in tobacco smokers and chewers. INTERPRETATION & CONCLUSIONS: Our results showed that oral cancer patients had significantly higher frequency of AA genotype but significantly lower frequency of AC genotype and C allele compared to controls. The IL-2 AC genotype and C allele of IL-2 (−330A>C) gene polymorphisms could be potential protective factors and might reduce the risk of oral cancer in Indian population.
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spelling pubmed-59263442018-05-08 Association of −330 interleukin-2 gene polymorphism with oral cancer Singh, Prithvi Kumar Kumar, Vijay Ahmad, Mohammad Kaleem Gupta, Rajni Mahdi, Abbas Ali Jain, Amita Bogra, Jaishri Chandra, Girish Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Cytokines play an important role in the development of cancer. Several single-nucleotide polymorphisms (SNPs) of cytokine genes have been reported to be associated with the development and severity of inflammatory diseases and cancer predisposition. This study was undertaken to evaluate a possible association of interleukin 2 (IL-2) (− 330A>C) gene polymorphisms with the susceptibility to oral cancer. METHODS: The SNP in IL-2 (−330A>C) gene was genotyped in 300 oral cancer patients and in similar number of healthy volunteers by polymerase chain reaction (PCR)-restriction fragment length polymorphism and the association of the gene with the disease was evaluated. RESULTS: IL-2 (−330A>C) gene polymorphism was significantly associated with oral cancer whereas it was neither associated with clinicopathological status nor with cancer pain. The AC heterozygous genotype was significantly associated with oral cancer patients as compared to controls [odds ratio (OR): 3.0; confidence interval (CI): 2.14-4.20; P<0.001]. The C allele frequency was also significantly associated with oral cancer (OR: 1.80; CI: 1.39-2.33; P<0.001). IL-2 (−330A>C) gene polymorphism was also associated with oral cancer in tobacco smokers and chewers. INTERPRETATION & CONCLUSIONS: Our results showed that oral cancer patients had significantly higher frequency of AA genotype but significantly lower frequency of AC genotype and C allele compared to controls. The IL-2 AC genotype and C allele of IL-2 (−330A>C) gene polymorphisms could be potential protective factors and might reduce the risk of oral cancer in Indian population. Medknow Publications & Media Pvt Ltd 2017-12 /pmc/articles/PMC5926344/ /pubmed/29664031 http://dx.doi.org/10.4103/ijmr.IJMR_1949_15 Text en Copyright: © 2017 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Singh, Prithvi Kumar
Kumar, Vijay
Ahmad, Mohammad Kaleem
Gupta, Rajni
Mahdi, Abbas Ali
Jain, Amita
Bogra, Jaishri
Chandra, Girish
Association of −330 interleukin-2 gene polymorphism with oral cancer
title Association of −330 interleukin-2 gene polymorphism with oral cancer
title_full Association of −330 interleukin-2 gene polymorphism with oral cancer
title_fullStr Association of −330 interleukin-2 gene polymorphism with oral cancer
title_full_unstemmed Association of −330 interleukin-2 gene polymorphism with oral cancer
title_short Association of −330 interleukin-2 gene polymorphism with oral cancer
title_sort association of −330 interleukin-2 gene polymorphism with oral cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926344/
https://www.ncbi.nlm.nih.gov/pubmed/29664031
http://dx.doi.org/10.4103/ijmr.IJMR_1949_15
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