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前列腺癌中的遗传标记。

Genetic markers in carcinoma of the prostate.

作者信息

Dimopoulos M A, Germenis A, Savides P, Karayanis A, Fertakis A, Dimopoulos C

出版信息

Eur Urol. 1984;10(5):315-6. doi: 10.1159/000463818.

Abstract

The distribution of phenotypes and gene frequencies of the third component of complement (C3), group-specific component (Gc), haptoglobin (Hp) and transferrin (Tf) were studied in 115 patients with carcinoma of the prostate. The statistical analysis of our findings in comparison to the frequency of these genes in a control group of 155 patients with benign prostatic hyperplasia does not reveal any correlation between the distribution of the Hp and Tf phenotypes and the disease. On the contrary, a statistically significant association was found between carcinoma of prostate and C3F and Gc2 genes. The relative risk incidence of this malignancy is 1.56 and 1.81, respectively, for the carriers of these genes suffering from benign prostate hyperplasia.

摘要

对115例前列腺癌患者的补体第三成分(C3)、组特异性成分(Gc)、触珠蛋白(Hp)和转铁蛋白(Tf)的表型分布及基因频率进行了研究。将我们的研究结果与155例良性前列腺增生患者对照组中这些基因的频率进行统计学分析,结果显示Hp和Tf表型分布与疾病之间无任何相关性。相反,发现前列腺癌与C3F和Gc2基因之间存在统计学上的显著关联。对于患有良性前列腺增生的这些基因携带者,这种恶性肿瘤的相对风险发生率分别为1.56和1.81。

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