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血管内皮生长因子基因多态性与结直肠癌患者预后的关系。

Prognostic significance of vascular endothelial growth factor gene polymorphisms in patients with colorectal cancer.

机构信息

Department of Internal Medicine, School of Medicine, CHA University, Seongnam, South Korea.

出版信息

Int J Clin Oncol. 2013 Dec;18(6):1032-41. doi: 10.1007/s10147-012-0493-6. Epub 2012 Nov 7.

Abstract

BACKGROUND

Angiogenesis plays an important role in tumor development, progression, and metastasis. Vascular endothelial growth factor (VEGF) is a key regulator of angiogenesis. However, the contribution of common VEGF polymorphisms to colorectal cancer (CRC) prognosis remains unclear.

METHODS

We have genotyped four polymorphisms of VEGF (-2578C>A, -1154G>A, -634G>C, and 936C>T) in 350 CRC cases from the Korean population. The genotyping of VEGF polymorphisms was performed by polymerase chain reaction-restriction fragment length polymorphism assay.

RESULTS

Although not every VEGF polymorphism was significantly correlated with patient prognosis in overall 350 CRC patients, we found that the VEGF -2578CA genotype was associated with a significantly poor prognosis for rectal cancers compared to the CC genotype (HR = 2.156; 95 % CI 1.090-4.267; P = 0.028). In addition, we found that the -2578A/-1154G/-634G/+936C haplotype was significantly associated with a decreased overall survival (OS) rate in all 350 CRC patients (HR = 2.530; 95 % CI 1.340-4.780; P = 0.004). In combination analysis, we found that the combined VEGF -2578CA+AA/-1154GG genotype was associated with a poor OS rate in all 350 CRC patients (HR = 2.068; 95 % CI 1.159-3.693; P = 0.015).

CONCLUSIONS

The VEGF gene polymorphisms investigated in this study were not found to be independent prognostic markers in Korean CRC populations. However, our results suggest that the VEGF -2578C>A variant may be a potential genetic marker for rectal cancer prognosis. Further large population studies are warranted to define whether the -2578C>A polymorphism is a prognostic marker of rectal cancer.

摘要

背景

血管生成在肿瘤的发生、发展和转移中起着重要作用。血管内皮生长因子(VEGF)是血管生成的关键调节因子。然而,常见的 VEGF 多态性对结直肠癌(CRC)预后的贡献尚不清楚。

方法

我们对来自韩国人群的 350 例 CRC 病例进行了 VEGF(-2578C>A、-1154G>A、-634G>C 和 936C>T)的四个多态性的基因分型。VEGF 多态性的基因分型通过聚合酶链反应-限制性片段长度多态性分析进行。

结果

尽管并非每个 VEGF 多态性在 350 例 CRC 患者的总体预后中都有显著相关性,但我们发现 VEGF-2578CA 基因型与直肠癌的预后显著较差相关,与 CC 基因型相比(HR=2.156;95%CI 1.090-4.267;P=0.028)。此外,我们发现-2578A/-1154G/-634G/+936C 单倍型与所有 350 例 CRC 患者的总生存(OS)率显著降低相关(HR=2.530;95%CI 1.340-4.780;P=0.004)。在联合分析中,我们发现 VEGF-2578CA+AA/-1154GG 基因型的组合与所有 350 例 CRC 患者的 OS 率较差相关(HR=2.068;95%CI 1.159-3.693;P=0.015)。

结论

本研究中研究的 VEGF 基因多态性在韩国 CRC 人群中不是独立的预后标志物。然而,我们的结果表明,VEGF-2578C>A 变体可能是直肠癌预后的潜在遗传标志物。需要进一步的大人群研究来确定-2578C>A 多态性是否是直肠癌的预后标志物。

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