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首页> 外文期刊>Alexandria Journal of Medicine >Physiological variables and molecular study of KLK2 and KLK3 among patient with benign prostatic hyperplasia
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Physiological variables and molecular study of KLK2 and KLK3 among patient with benign prostatic hyperplasia

机译:前列腺增生患者 KLK2 KLK3 的生理变量和分子研究

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摘要

Prostatic hyperplasia is benign tumor occur in prostate. Benign prostatic hyperplasia is common disease in old men. The incidence of disease arises with increase in age. The patient with benign prostatic hyperplasia are estimated 20% of men in 40s old, and 90% in of men in 80s old, and main causes of prostatic hyperplasia are unknown but there is evidence referring to genetic and hormonal disorders that may cause the disease. This study includes 60 patients with prostatic hyperplasia with an average age of 64years old and 30 samples as a control with same age group. The study obtained that there was significant association (P≤0.05) between PSA (KLK3) and prostatic hyperplasia. Result also mentions that there was significant decrease in testosterone level and significant increase in dihydrotestosterone level. The present study for KLK2 and KLK3 genes showed molecular variation in both genes, varied between polymorphism and allele polymorphism. PCR amplification of specific primers of KLK2 gene showed polymorphisms ranged between 14%, 8%, 10%, and 6% in each KLK2a, KLK2b, KLK2c, and KLK2d primers respectively, while the allele polymorphism in KLK2c amplification with primer reaches 18% of patient. PCR amplification of specific primers of KLK3 gene showed polymorphisms ranged between 10%, 6%, 2%, and 4% in each KLK3a, KLK3b, KLK3c, and KLK3d primer respectively, and allele variation was not detected in amplification product of KLK3 .
机译:前列腺增生是良性肿瘤发生在前列腺。良性前列腺增生是老年男性的常见疾病。疾病的发生随着年龄的增长而增加。患有前列腺增生的患者估计在40岁以下的男性中占20%,在80岁以上的男性中占90%,前列腺增生的主要原因尚不清楚,但有证据表明可能导致该疾病的遗传和激素紊乱。这项研究包括60例前列腺增生患者,平均年龄为64岁,并以30个样本作为同一年龄组的对照组。研究发现PSA(KLK3)与前列腺增生之间存在显着相关性(P≤0.05)。结果还提到,睾丸激素水平显着下降,二氢睾丸激素水平显着上升。目前对KLK2和KLK3基因的研究表明两个基因的分子变异,在多态性和等位基因多态性之间变化。 KLK2基因特异性引物的PCR扩增显示,每个KLK2a,KLK2b,KLK2c和KLK2d引物的多态性分别在14%,8%,10%和6%之间,而KLK2c扩增的等位基因多态性达到引物的18%。患者。 KLK3基因特异性引物的PCR扩增显示,每个KLK3a,KLK3b,KLK3c和KLK3d引物的多态性分别在10%,6%,2%和4%之间,并且在KLK3的扩增产物中未检测到等位基因变异。

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