Ankathil Ravindran, Mustapha Mohd Aminudin, Abdul Aziz Ahmad Aizat, Mohd Shahpudin Siti Nurfatimah, Zakaria Andee Dzulkarnaen, Abu Hassan Muhammad Radzi, Musa Kamarul Imran
Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Kelantan, Malaysia. Email: Email:
Center of Pre University Study, Universiti Malaysia Sarawak, Kota Samarahan, Sarawak, Malaysia.
Asian Pac J Cancer Prev. 2019 Jun 1;20(6):1621-1632. doi: 10.31557/APJCP.2019.20.6.1621.
To investigate the frequencies and association of polymorphic genotypes of IL-8 -251 T>A, TNF-α -308 G>A, ICAM-1 K469E, ICAM-1 R241G, IL-6 -174 G>C, and PPAR-γ 34 C>G in modulating susceptibility risk in Malaysian colorectal cancer (CRC) patients. Methods: In this case-control study, peripheral blood samples of 560 study subjects (280 CRC patients and 280 controls) were collected, DNA extracted and genotyped using PCR-RFLP and Allele Specific PCR. The association between polymorphic genotype and CRC susceptibility risk was determined using Logistic Regression analysis deriving Odds ratio (OR) and 95% CI. Results: On comparing the frequencies of genotypes of all single nucleotide polymorphisms ( SNPs ) in patients and controls, the homozygous variant genotypes IL-8 -251 AA and TNF-α -308 AA and variant A alleles were significantly higher in CRC patients. Investigation on the association of the variant alleles and genotypes singly, with susceptibility risk showed the homozygous variant A alleles and genotypes IL-8 -251 AA and TNF-α -308 AA to be at higher risk for CRC predisposition. Analysis based on age, gender and smoking habits showed that the polymorphisms IL8 -251 T>A and TNF – α 308 G>A contribute to a significantly higher risk among male and female who are more than 50 years and for smokers in this population. Conclusion: We observed an association between variant allele and genotypes of IL-8-251 T>A and TNF-α-308 G>A polymorphisms and CRC susceptibility risk in Malaysian patients. These two SNPs in inflammatory response genes which undoubtedly contribute to individual risks to CRC susceptibility may be considered as potential genetic predisposition factors for CRC in Malaysian population.
研究白细胞介素-8(IL-8)-251T>A、肿瘤坏死因子-α(TNF-α)-308G>A、细胞间黏附分子-1(ICAM-1)K469E、ICAM-1 R241G、白细胞介素-6(IL-6)-174G>C和过氧化物酶体增殖物激活受体-γ(PPAR-γ)34C>G的多态性基因型在调节马来西亚结直肠癌(CRC)患者易感性风险中的频率及相关性。方法:在这项病例对照研究中,收集了560名研究对象(280例CRC患者和280名对照)的外周血样本,提取DNA并使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和等位基因特异性PCR进行基因分型。使用逻辑回归分析得出优势比(OR)和95%置信区间(CI),以确定多态性基因型与CRC易感性风险之间的关联。结果:比较患者和对照中所有单核苷酸多态性(SNP)的基因型频率时,CRC患者中纯合变异基因型IL-8 -251 AA和TNF-α -308 AA以及变异A等位基因显著更高。单独研究变异等位基因和基因型与易感性风险的关联时,纯合变异A等位基因以及基因型IL-8 -251 AA和TNF-α -308 AA患CRC的易感性风险更高。基于年龄、性别和吸烟习惯的分析表明,IL8 -251 T>A和TNF – α 308 G>A多态性在该人群中50岁以上的男性和女性以及吸烟者中导致的风险显著更高。结论:我们观察到IL-8-251 T>A和TNF-α-308 G>A多态性的变异等位基因和基因型与马来西亚患者的CRC易感性风险之间存在关联。这两个炎症反应基因中的单核苷酸多态性无疑会增加个体患CRC的易感性风险,可被视为马来西亚人群中CRC潜在的遗传易感性因素。