The -308G/A polymorphism of the tumor necrosis factor-alpha gene is associated with the risk of upper aerodigestive tract cancer: a meta-analysis.

The -308G/A polymorphism of the tumor necrosis factor-alpha gene is associated with the risk of upper aerodigestive tract cancer: a meta-analysis.
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肿瘤坏死因子-α 基因的 -308G/A 多态性与上呼吸消化道癌症的风险相关:一项荟萃分析。

DOI:
10.1620/tjem.229.245
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发表时间:
2013
期刊:
The Tohoku journal of experimental medicine
影响因子:
--
通讯作者:
Qianming Chen
Qianming Chen
中科院分区:
--
文献类型:
--
作者:
Jiayi Wang;Xin Jin;Hui Wang;Jiantang Yang;Li;Lei Lei;Xiaoxu Li;Yu Zhou;X. Zeng;Lu Jiang;Ga Liao;H. Dan;Qianming Chen

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肿瘤坏死因子-α(TNF-α)已被认为有助于上呼吸消化道(UADT)癌症的发展,其特征是预后不良。TNF-α基因-308G/A多态性(-308G/A多态性)可增加TNF-α的表达水平,从而影响UADT癌的遗传易感性。-308G/A多态性与UADT癌症之间的关联已被广泛研究,但已发表的结果相当有争议。为了获得更准确的结论,我们进行了一项荟萃分析,包括1,751名患者和3,345名对照。结果表明,与G携带者(GG和GA基因型)相比,-308G/A基因AA型患UADT癌的风险增加54%[OR = 1.54,95%可信区间(CI):1.07-2.21]。按种族分层后,AA基因型与南亚人UADT癌症风险增加相关(AA vs. GA+GG的OR = 33.18和95%CI:1.92-573.62),但与高加索人或东亚人无关。按肿瘤部位分层后,-308G/A多态性与口咽癌风险增加相关(AA与GA+GG的OR = 2.68和95%CI:1.34-5.35),但与食管癌和喉癌无关。按组织学类型分层后,-308G/A多态性与鳞状细胞癌的风险增加相关(AA与GA+GG的OR = 1.81和95%CI:1.15-2.84),但与腺癌无关。我们的研究结果表明,-308G/A多态性可能有助于UADT癌症易感性的风险增加。
Tumor necrosis factor-alpha (TNF-α) has been proposed to contribute to the development of upper aerodigestive tract (UADT) cancer that is characterized by poor prognosis. The G-to-A nucleotide change at -308 of the TNF-α gene (-308G/A polymorphism) can increase the expression level of TNF-α and thus may affect the genetic susceptibility of UADT cancer. The association between the -308G/A polymorphism and UADT cancer has been widely studied, but the results published are quite controversial. To obtain a more precise conclusion, we performed a meta-analysis including 1,751 patients and 3,345 controls. The results indicated that the AA genotype of the -308G/A polymorphism had a 54%-increased risk of UADT cancer, compared with the G carriers (GG and GA genotypes) [odds ratio (OR) = 1.54, 95% confidence interval (CI): 1.07-2.21]. After stratified by ethnicity, the AA genotype was associated with increased risk of UADT cancers in South Asians (OR = 33.18 and 95% CI: 1.92-573.62 for AA vs. GA+GG) but not in Caucasians or East Asians. After stratified by tumor site, the -308G/A polymorphism was associated with increased risks of oropharynx cancer (OR = 2.68 and 95% CI: 1.34-5.35 for AA vs. GA+GG) but not associated with esophagus or larynx cancer. After stratified by histological type, the -308G/A polymorphism was associated with increased risks of squamous cell carcinoma (OR = 1.81 and 95% CI: 1.15-2.84 for AA vs. GA+GG) but not associated with adenocarcinoma. Our results indicate that the -308G/A polymorphism might contribute to an increased risk of UADT cancer susceptibility.
DOI: 10.1086/323612
发表时间: 2001-10-01
影响因子: 9.8
作者:
Frisse, L;Hudson, RR;Di Rienzo, A
通讯作者: Di Rienzo, A
DOI: 10.1182/blood-2006-06-026385
发表时间: 2007-04-15
期刊: BLOOD
影响因子: 20.3
作者:
Xu, Jun;Chakrabarti, Ayan K.;Vujanovic, Nikola L.
通讯作者: Vujanovic, Nikola L.