首页> 外文期刊>The Tohoku Journal of Experimental Medicine >The -765C allele of the cyclooxygenase-2 gene as a potential risk factor of colorectal cancer: a meta-analysis.
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The -765C allele of the cyclooxygenase-2 gene as a potential risk factor of colorectal cancer: a meta-analysis.

机译:环氧合酶2基因的-765C等位基因是结直肠癌的潜在危险因素:一项荟萃分析。

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Colorectal cancer (CRC) is the third leading cause of cancer-related death in the world. Human colorectal carcinogenesis is a complex, multistep and multigenetic process. Cyclooxygenase-2 (COX2), a key enzyme in arachidonic acid metabolism, is overexpressed in several epithelial malignancies including colorectal cancer. COX2 expression can be induced by pro-inflammatory and mitogenic stimuli. The -765G/C polymorphism of the COX2 gene promoter has been reported to affect CRC susceptibility, but recent studies have demonstrated conflicting results. To shed light on these inconclusive findings, we performed a meta-analysis for assessing the involvement of COX2 -765G/C polymorphisms at the onset of colorectal carcinoma. Literature-based searching was guided to gather data and either fixed-effect or random-effect model was used to pool the odds ratio (OR) according to the test of heterogeneity. The 10 eligible case-control studies included 3,322 colorectal cancer cases and 5,166 controls. Overall, no evidence has indicated that individuals carrying GC+CC genotypes had significantly increased colorectal cancer risk compared with GG genotype [OR = 1.06, 95% confidence interval (95% CI) = 0.94-1.20]. However, stratified analysis with ethnicity indicated that individuals carrying GC+CC genotypes had an increased risk of colorectal cancer (OR = 1.40, 95% CI = 1.11-1.76) among Asian population. In conclusion, although not all bias could be eliminated, the -765C allele of the COX2 gene may be a potential risk factor for colorectal cancer in Asians.
机译:大肠癌(CRC)是世界上与癌症相关的死亡的第三大主要原因。人类结肠直肠癌变是一个复杂,多步骤,多基因的过程。花生四烯酸代谢中的关键酶环氧合酶2(COX2)在包括结肠直肠癌在内的多种上皮恶性肿瘤中过表达。可以通过促炎和促有丝分裂刺激来诱导COX2表达。据报道,COX2基因启动子的-765G / C多态性会影响CRC的易感性,但最近的研究证明了相互矛盾的结果。为了阐明这些不确定的发现,我们进行了荟萃分析,以评估结肠直肠癌发作时COX2 -765G / C多态性的参与情况。引导基于文献的搜索来收集数据,并根据异质性测试使用固定效应模型或随机效应模型合并优势比(OR)。十项符合条件的病例对照研究包括3,322例大肠癌病例和5,166例对照。总体而言,没有证据表明与GG基因型相比,携带GC + CC基因型的个体患结直肠癌的风险显着增加[OR = 1.06,95%置信区间(95%CI)= 0.94-1.20]。但是,按种族进行的分层分析表明,携带GC + CC基因型的个体在亚洲人群中患结直肠癌的风险增加(OR = 1.40,95%CI = 1.11-1.76)。总之,尽管不能消除所有偏倚,但COX2基因的-765C等位基因可能是亚洲人结直肠癌的潜在危险因素。

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