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首页> 外文期刊>OncoTargets and therapy >Association between the Cyclin D1 G870A polymorphism and the susceptibility to and prognosis of upper aerodigestive tract squamous cell carcinomas: an updated meta-analysis
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Association between the Cyclin D1 G870A polymorphism and the susceptibility to and prognosis of upper aerodigestive tract squamous cell carcinomas: an updated meta-analysis

机译:Cyclin D 1 G870A基因多态性与上消化道鳞状细胞癌易感性和预后的关系:最新荟萃分析

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Purpose: Several publications have investigated the association between the Cyclin D1 G to A substitution at nucleotide 870 (CCND1 G870A) polymorphism and squamous cell carcinoma (SCC) of the upper aerodigestive tract (UADT), but their conclusions still remain controversial. We conducted a meta-analysis to precisely evaluate this association. Patients and methods: We electronically searched the Chinese National Knowledge Infrastructure, PubMed, and Embase (up to January 2015) databases for case–control studies on the association between the CCND1 G870A polymorphism and SCC of the UADT, and 23 studies were included in total. Results: The meta-analysis results showed that there was a significant association between the CCND1 G870A polymorphism and the risk of SCC of the UADT (AA vs GG: odds ratio [OR]?=1.33, 95% confidence interval [CI] =1.01–1.74, P <0.001 for heterogeneity; GA/AA vs GG: OR =1.24, 95% CI =1.01–1.51, P <0.001 for heterogeneity; AA vs GA/GG: OR?=1.16, 95% CI =0.97–1.39, P <0.001 for heterogeneity; allele A vs allele G: OR =1.14, 95% CI?=1.00–1.30, P <0.001 for heterogeneity; GA vs GG: OR =1.18, 95% CI =0.98–1.42, P <0.001 for heterogeneity). However, when analyzing prognosis, allele G was a potential risk factor for poor tumor differentiation (AA vs GA/GG: OR =2.60, 95% CI =1.15–5.86, P =0.836 for heterogeneity) and reduced disease-free intervals (OR =2.08, 95% CI =1.17–3.69, P =0.134 for heterogeneity). In the subgroup analysis, the cancer susceptibility of Asian groups, population-based control groups, nasopharyngeal cancer groups, and esophageal SCC groups were more likely to be affected by the CCND1 G870A polymorphism. No significant publication bias was found in our analysis ( P =0.961 for Egger’s test and P =0.245 for Begg’s test). Conclusion: The results of the present meta-analysis suggest that the variant CCND1 870A allele might confer an elevated risk of SCC of the UADT, particularly among Asians and individuals who have esophageal or nasopharyngeal cancers. Moreover, the CCND1 870A allele might also confer better tumor differentiation grades and longer disease-free intervals.
机译:目的:几篇文献研究了Cyclin D 1 G与核苷酸870(CCND1 G870A)多态性与上呼吸消化道鳞癌(UADT)之间的联系,但它们与结论仍存在争议。我们进行了荟萃分析以精确评估这种关联。患者和方法:我们以电子方式搜索了中国国家知识基础设施,PubMed和Embase数据库(截至2015年1月),以进行CCND1 G870A多态性与UADT SCC之间关联的病例对照研究,总共包括23项研究。结果:荟萃分析结果表明,CCND1 G870A多态性与UADT的SCC风险之间存在显着相关性(AA与GG:优势比[OR]?= 1.33,95%置信区间[CI] = 1.01) –1.74,异质性的P <0.001; GA / AA与GG:OR = 1.24,95%CI = 1.01-1.51,异质性的P <0.001; AA与GA / GG:OR?= 1.16,95%CI = 0.97– 1.39,异质性的P <0.001;等位基因A与等位基因G:OR = 1.14,95%CI?= 1.00-1.30,异质性P <0.001; GA与GG:OR = 1.18,95%CI = 0.98-1.42,P异质性<0.001)。然而,在分析预后时,等位基因G是导致肿瘤分化差的潜在危险因素(AA vs GA / GG:OR = 2.60,95%CI = 1.15–5.86,异质性P = 0.836)和无病间隔期缩短(OR = 2.08,95%CI = 1.17–3.69,异质性P = 0.134)。在亚组分析中,亚洲人群,以人群为基础的对照组,鼻咽癌组和食管鳞癌组的癌症易感性更可能受到CCND1 G870A多态性的影响。在我们的分析中,没有发现明显的出版偏倚(Egger检验为P = 0.961,Begg检验为P = 0.245)。结论:本荟萃分析的结果表明,变异CCND1 870A等位基因可能使UADT的SCC风险升高,特别是在亚洲人和患有食道或鼻咽癌的个体中。此外,CCND1 870A等位基因还可能赋予更好的肿瘤分化等级和更长的无病间隔时间。

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