Division of Clinical Oncology, Department of Internal Medicine, Medical University Graz, Auenbruggerplatz 15, 8036 Graz, Austria.
Anticancer Res. 2012 Aug;32(8):3473-8.
Recent data suggest that erythropoietin (EPO) plays a substantial role in cancer development and clinical outcome by stimulating cell proliferation, invasion and angiogenesis. A functional polymorphism (rs1617640 G>T) in the promoter region of the EPO gene increases EPO protein expression. In the present study, we investigated the association of EPO rs1617640 G>T with susceptibility and clinical outcome of early-stage breast cancer. Genomic DNA of 539 female patients with histologically confirmed early-stage breast cancer and 804 controls was genotyped for EPO rs1617640 G>T. No association was found between EPO rs1617640 G>T and early-stage breast cancer susceptibility and clinical outcome (hazard ratio=1.24, 95% confidence interval=1.82-1.90, p=0.31). In conclusion, our findings suggest a lack of influence of EPO rs1617640 G>T on early-stage breast carcinogenesis and clinical outcome.
最近的数据表明,促红细胞生成素(EPO)通过刺激细胞增殖、侵袭和血管生成在癌症发展和临床结局中发挥重要作用。EPO 基因启动子区域的一个功能性多态性(rs1617640 G>T)增加了 EPO 蛋白的表达。在本研究中,我们调查了 EPO rs1617640 G>T 与早期乳腺癌易感性和临床结局的关系。对 539 名经组织学证实的早期乳腺癌女性患者和 804 名对照的基因组 DNA 进行了 EPO rs1617640 G>T 的基因分型。EPO rs1617640 G>T 与早期乳腺癌易感性和临床结局之间没有关联(风险比=1.24,95%置信区间=1.82-1.90,p=0.31)。总之,我们的研究结果表明 EPO rs1617640 G>T 对早期乳腺癌的发生和临床结局没有影响。