Polymorphism in the tumor necrosis factor alpha promoter region and its influence on colorectal cancer predisposition risk in Malaysian population

objective:A case control study was designed to investigate the TNF-a -308 G>A polymorphism allele frequencies and to determine the influence of the polymorphic genotype on sporadic CRC susceptibility risk in Malaysia population. Material and methods: Peripheral blood samples of 164 normal contro...

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Main Authors: Mohd Aminudin, Mustapha, Siti Nurfatimah, Mohd Shahpudin, Ahmad Aizat, Abdul Aziz, Bhavaraju, Venkata Muralikrishna, Naik, Venkatesh R, Zaidi, Zakaria, Ahmad Shanwani, Mohd Sidek, Mohammad Radzi, Abu Hasan, Ankathil, Ravindran
Format: E-Article
Language:English
Published: Japan International Cultural Exchange Foundation (JICEF), 2011
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Online Access:http://ir.unimas.my/id/eprint/706/1/Polymorphism%20in%20the%20tumor%20necrosis%20factor%20alpha%20promoter.pdf
http://ir.unimas.my/id/eprint/706/
http://www.seronjihou.co.jp/imj/
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Institution: Universiti Malaysia Sarawak
Language: English
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Summary:objective:A case control study was designed to investigate the TNF-a -308 G>A polymorphism allele frequencies and to determine the influence of the polymorphic genotype on sporadic CRC susceptibility risk in Malaysia population. Material and methods: Peripheral blood samples of 164 normal controls and 161 clinically and histopathhologically confirm CRC patients were genotyped for TNF-a -308 G>A polymorphism employing allele specific PCR. The relative associations of various genotypes with CRC susceptibility risk was determined by calculating Odd ratios. Corresponding Chi-square tests on CRC patients and controls were carried out and 95% confidence interval (95% CI) were determined using fisher exact tests. Results: On comparing the frequencies of genotypes of patients and controls, the homozygous variant AA was significabtly higher in CRC patients (p=0.030) compared to controls. On investigating the association of the polymorphic genotypes with CRC susceptibility risk, the homozygous variant TNF-a -308AA showed significantly increased risk with OR 2.5842. Conclusion: Our results suggest that, polymorphic genotype of inflammation response gene TNF-a is significantly associated with CRC susceptibility risk and colud be considered as a high risk variant for CRC predisposition.