首页> 外文期刊>The pharmacogenomics journal >VEGF -460T --> C polymorphism and its association with VEGF expression and outcome to FOLFOX-4 treatment in patients with colorectal carcinoma.
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VEGF -460T --> C polymorphism and its association with VEGF expression and outcome to FOLFOX-4 treatment in patients with colorectal carcinoma.

机译:结直肠癌患者中VEGF -460T-> C多态性及其与VEGF表达和FOLFOX-4治疗结局的关系。

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    摘要

    The -460T --> C polymorphism of vascular endothelial growth factor (VEGF) gene significantly increases its promoter activity. A pilot study was conducted to assess the influence of this polymorphism on clinicopathological features of patients with colorectal carcinoma. In total, 228 patients were enrolled, including 100 with stage II/III colorectal carcinoma receiving curative surgery and 128 with metastatic disease. An excellent correlation in VEGF -460 genotypes based on white blood cells and tumor tissues existed, but there was no between-group difference in patients with or without colorectal carcinoma. A marked increase in intratumor and circulating VEGF levels were observed in patients with the T/C or C/C genotypes (P < 0.01), which was associated with increased extent of invasion, nodal involvement, poor histological differentiation, subsequent metastasis and shorter survival in stage II/III patients treated with curative surgery (P < 0.01). For patients with metastatic disease, this polymorphism was associated with a lower response rate to FOLFOX-4 (P = 0.03) and shorter survival (P < 0.001). By multivariate analysis, this polymorphism was identified as an independent prognostic factor (P = 0.01). These data suggest that -460T --> C polymorphism of VEGF gene, by increasing VEGF expression and subsequent angiogenesis, could be a key determinant for increased tumor recurrence and a poor prognosis of patients with colorectal carcinoma. However, this study is exploratory and is not adjusted for multiple comparisons, requiring independent replication.
    机译:血管内皮生长因子(VEGF)基因的-460T-> C多态性显着提高了其启动子活性。进行了一项初步研究,以评估这种多态性对结直肠癌患者临床病理特征的影响。总共招募了228名患者,包括100例接受根治性手术的II / III期大肠癌和128例转移性疾病。基于白细胞和肿瘤组织的VEGF -460基因型之间存在极好的相关性,但是在有或没有大肠癌的患者中,组间没有差异。 T / C或C / C基因型患者的肿瘤内和循环VEGF水平显着增加(P <0.01),这与浸润程度增加,淋巴结转移,组织学分化差,随后转移和生存期缩短有关在接受根治性手术治疗的II / III期患者中(P <0.01)。对于患有转移性疾病的患者,这种多态性与对FOLFOX-4的响应率较低(P = 0.03)和生存期较短(P <0.001)有关。通过多变量分析,该多态性被确定为独立的预后因素(P = 0.01)。这些数据表明,通过增加VEGF表达和随后的血管生成,VEGF基因的-460T→C多态性可能是导致大肠癌患者肿瘤复发增加和预后不良的关键因素。但是,该研究是探索性的,并未针对多个比较进行调整,需要独立复制。

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