The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.

Objective: To investigate the allele and genotype frequencies of NFKBI -94 ins/de! ATTG (rs28720239) polymorphism and to evaluate the association between the polymorphism and colorectal cancer (CRC) risk in Malaysian population. Methods: Genomic DNA was extracted from the peripheral blood samples of...

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Main Authors: Mohd Suzairi, M.S., Tan, S.C., Ahmad Aizat, Abdul Aziz, Mohd Aminudin, Mustapha, Siti Nurfatimah, Mohd Shahpudin, Andee, Z.D., Ankathil, Ravindran
Format: Article
Language:English
Published: Elsevier Science, Ltd. 2013
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Online Access:http://ir.unimas.my/id/eprint/30234/1/The%20functional%20.pdf
http://ir.unimas.my/id/eprint/30234/
https://www.sciencedirect.com/science/article/abs/pii/S1877782113000945
https://doi.org/10.1016/j.canep.2013.05.007
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spelling my.unimas.ir.302342023-07-31T03:37:42Z http://ir.unimas.my/id/eprint/30234/ The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer. Mohd Suzairi, M.S. Tan, S.C. Ahmad Aizat, Abdul Aziz Mohd Aminudin, Mustapha Siti Nurfatimah, Mohd Shahpudin Andee, Z.D. Ankathil, Ravindran Q Science (General) R Medicine (General) Objective: To investigate the allele and genotype frequencies of NFKBI -94 ins/de! ATTG (rs28720239) polymorphism and to evaluate the association between the polymorphism and colorectal cancer (CRC) risk in Malaysian population. Methods: Genomic DNA was extracted from the peripheral blood samples of 474 study subjects, which consisted of 237 histopathologically confirmed CRC patients and an equal number of cancer-free controls. The NFKBI -94 ins/de! ATTG (rs28720239) polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and confirmed by DNA sequencing. The association between the polymorphic genotypes and CRC risk was evaluated by deriving odds ratios (ORs) and 95% confidence intervals (Cls) using unconditional logistic regression analysis. Results: The frequencies of wildtype (del/del), heterozygous ( del/ins) and variant (ins/ins) genotypes in CRC patients were 31.7%, 53.6% and 14.8%, respectively, while those in cancer-free controls were 35.0%, 58.2% and 6.8%, respectively. The frequency of the variant genotype was significantly higher in cases compared to controls (P < 0.01 ). Evaluation of the risk association of the polymorphic genotypes revealed that the variant genotype could contribute to a significantly increased risk of CRC (OR= 2.42, 95% CI= 1.24-4.73, P < 0.01 ). Conclusions: The variant allele of NFKBI -94 ins/de! ATTG (rs28362491) polymorphism is associated with higher risk of sporadic CRC in Malaysian population. Elsevier Science, Ltd. 2013-06 Article PeerReviewed text en http://ir.unimas.my/id/eprint/30234/1/The%20functional%20.pdf Mohd Suzairi, M.S. and Tan, S.C. and Ahmad Aizat, Abdul Aziz and Mohd Aminudin, Mustapha and Siti Nurfatimah, Mohd Shahpudin and Andee, Z.D. and Ankathil, Ravindran (2013) The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer. Cancer Epidemiology, 37 (5). pp. 634-638. ISSN 1877-7821 https://www.sciencedirect.com/science/article/abs/pii/S1877782113000945 https://doi.org/10.1016/j.canep.2013.05.007
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic Q Science (General)
R Medicine (General)
spellingShingle Q Science (General)
R Medicine (General)
Mohd Suzairi, M.S.
Tan, S.C.
Ahmad Aizat, Abdul Aziz
Mohd Aminudin, Mustapha
Siti Nurfatimah, Mohd Shahpudin
Andee, Z.D.
Ankathil, Ravindran
The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
description Objective: To investigate the allele and genotype frequencies of NFKBI -94 ins/de! ATTG (rs28720239) polymorphism and to evaluate the association between the polymorphism and colorectal cancer (CRC) risk in Malaysian population. Methods: Genomic DNA was extracted from the peripheral blood samples of 474 study subjects, which consisted of 237 histopathologically confirmed CRC patients and an equal number of cancer-free controls. The NFKBI -94 ins/de! ATTG (rs28720239) polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and confirmed by DNA sequencing. The association between the polymorphic genotypes and CRC risk was evaluated by deriving odds ratios (ORs) and 95% confidence intervals (Cls) using unconditional logistic regression analysis. Results: The frequencies of wildtype (del/del), heterozygous ( del/ins) and variant (ins/ins) genotypes in CRC patients were 31.7%, 53.6% and 14.8%, respectively, while those in cancer-free controls were 35.0%, 58.2% and 6.8%, respectively. The frequency of the variant genotype was significantly higher in cases compared to controls (P < 0.01 ). Evaluation of the risk association of the polymorphic genotypes revealed that the variant genotype could contribute to a significantly increased risk of CRC (OR= 2.42, 95% CI= 1.24-4.73, P < 0.01 ). Conclusions: The variant allele of NFKBI -94 ins/de! ATTG (rs28362491) polymorphism is associated with higher risk of sporadic CRC in Malaysian population.
format Article
author Mohd Suzairi, M.S.
Tan, S.C.
Ahmad Aizat, Abdul Aziz
Mohd Aminudin, Mustapha
Siti Nurfatimah, Mohd Shahpudin
Andee, Z.D.
Ankathil, Ravindran
author_facet Mohd Suzairi, M.S.
Tan, S.C.
Ahmad Aizat, Abdul Aziz
Mohd Aminudin, Mustapha
Siti Nurfatimah, Mohd Shahpudin
Andee, Z.D.
Ankathil, Ravindran
author_sort Mohd Suzairi, M.S.
title The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
title_short The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
title_full The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
title_fullStr The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
title_full_unstemmed The functional -94 insertion/deletion ATTG polymorphism in the promoter region of NFKB1 gene increases the risk of sporadic colorectal cancer.
title_sort functional -94 insertion/deletion attg polymorphism in the promoter region of nfkb1 gene increases the risk of sporadic colorectal cancer.
publisher Elsevier Science, Ltd.
publishDate 2013
url http://ir.unimas.my/id/eprint/30234/1/The%20functional%20.pdf
http://ir.unimas.my/id/eprint/30234/
https://www.sciencedirect.com/science/article/abs/pii/S1877782113000945
https://doi.org/10.1016/j.canep.2013.05.007
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