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转醛醇酶1基因变异与头颈部鳞状细胞癌风险

Genetic variation in Transaldolase 1 and risk of squamous cell carcinoma of the head and neck.

作者信息

Basta Patricia V, Bensen Jeannette T, Tse Chiu-Kit, Perou Charles M, Sullivan Patrick F, Olshan Andrew F

机构信息

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7435, USA.

出版信息

Cancer Detect Prev. 2008;32(3):200-8. doi: 10.1016/j.cdp.2008.08.008. Epub 2008 Sep 20.

Abstract

BACKGROUND

The Pentose Phosphate Pathway (PPP) is involved in the body's protection against oxidative stress and resistance/susceptibility to apoptosis and thus has been implicated in tumor development and progression. Here we present data examining the association of genetic variation in one of the key enzymes of the PPP, Transaldolase 1 (TALDO1) with squamous cell carcinoma of the head and neck (SCCHN).

METHODS

We performed sequencing analysis to identify common genetic variations in TALDO1 and then investigated their association with SCCHN using samples from a population-based case/control study with both European American (EA) and African American (AA) former and current smokers.

RESULTS

We identified three polymorphisms in TALDO1 that were associated with SCCHN risk in our EA study population. Specifically the 5' upstream variant -490C>G or T (rs10794338), which we identified as tri-allelic, showed a reduced risk compared with any presence of the common allele, odds ratio (OR) [95% confidence interval (95% CI)]: 0.57 (0.38-0.86). Additionally two intronic high frequency polymorphisms demonstrated a positive association with disease, with the presence of the variant IVS1+1874T>A (rs3901233), 1.76 (1.19-2.61) and IVS4+2187A>C (rs4963163), 1.71 (1.16-2.53).

CONCLUSION

These results provide preliminary evidence that genetic polymorphisms in TALDO1 are associated with SCCHN.

摘要

背景

磷酸戊糖途径(PPP)参与机体对抗氧化应激以及对凋亡的抵抗/易感性,因此与肿瘤的发生和发展有关。在此,我们展示了有关PPP关键酶之一转醛醇酶1(TALDO1)的基因变异与头颈部鳞状细胞癌(SCCHN)关联的数据。

方法

我们进行了测序分析以鉴定TALDO1中的常见基因变异,然后使用来自基于人群的病例/对照研究的样本,对欧美裔(EA)和非裔美国人(AA)的既往和当前吸烟者进行研究,以调查它们与SCCHN的关联。

结果

在我们的EA研究人群中,我们鉴定出TALDO1中的三种多态性与SCCHN风险相关。具体而言,我们鉴定为三等位基因的5'上游变体-490C>G或T(rs10794338),与任何常见等位基因的存在相比,风险降低,优势比(OR)[95%置信区间(95%CI)]:0.57(0.38-0.86)。此外,两个内含子高频多态性与疾病呈正相关,变体IVS1+1874T>A(rs3901233)的存在,OR为1.76(1.19-2.61),IVS4+2187A>C(rs4963163)的OR为1.71(1.16-2.53)。

结论

这些结果提供了初步证据,表明TALDO1中的基因多态性与SCCHN有关。

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