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雄激素受体基因的串联CAG重复序列与黑人和白人男性的前列腺癌风险

Tandem CAG repeats of the androgen receptor gene and prostate cancer risk in black and white men.

作者信息

Panz V R, Joffe B I, Spitz I, Lindenberg T, Farkas A, Haffejee M

机构信息

Department of Medicine, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Endocrine. 2001 Jul;15(2):213-6. doi: 10.1385/ENDO:15:2:213.

Abstract

The most common malignancy in men worldwide is cancer of the prostate. Androgens play a direct role in normal and malignant growth of prostate cells via the androgen receptor (AR). This study analyzed the polymorphic CAG repeat sequence in exon 1 of the AR gene to determine if the number of repeats might be an indicator of prostate cancer risk or aggressive disease. DNA was extracted from blood samples of 20 black and 20 white men with well-documented prostate cancer and 40 healthy controls (20 blacks and 20 whites). PCR amplification was followed by gel electrophoresis and DNA sequencing. This region normally contains between 9 and 29 repeats. Patients and controls both had minor variations in the number of repeats, which ranged from 13 to 27 with 21 being the most frequent allele. Black controls and patients both had a mean of 20 +/- 3 repeats; in whites the mean was significantly lower in patients than controls (21 +/- 2 versus 23 +/- 2; p = 0.004). Combined black and white patients also had a lower number than the combined group of controls (20 +/- 3 versus 22 +/- 3; p = 0.02). Similarly, black and white patients with aggressive disease had a lower number than patients whose disease was more slowly progressive (19 +/- 2 versus 22 +/- 3; p = 0.02). We conclude that the small differences in the number of CAG repeats in both black and white patients do not appear to be a strong indicator of risk or aggressive disease but that this size polymorphism may be one of many genetic and environmental risk factors involved in prostate cancer.

摘要

前列腺癌是全球男性中最常见的恶性肿瘤。雄激素通过雄激素受体(AR)在前列腺细胞的正常生长和恶性生长中发挥直接作用。本研究分析了AR基因外显子1中的多态性CAG重复序列,以确定重复次数是否可能是前列腺癌风险或侵袭性疾病的一个指标。从20名患有前列腺癌且病历记录完备的黑人男性和20名白人男性以及40名健康对照者(20名黑人与20名白人)的血样中提取DNA。进行PCR扩增后进行凝胶电泳和DNA测序。该区域通常含有9至29个重复序列。患者和对照者在重复次数上均有微小差异,范围为13至27次,其中21次是最常见的等位基因。黑人对照者和患者的平均重复次数均为20±3次;在白人中,患者的平均重复次数显著低于对照者(分别为21±2次和23±2次;p = 0.004)。黑人与白人患者合并组的重复次数也低于对照组合并组(分别为20±3次和22±3次;p = 0.02)。同样,患有侵袭性疾病的黑人和白人患者的重复次数低于疾病进展较慢的患者(分别为19±2次和22±3次;p = 0.02)。我们得出结论,黑人和白人患者中CAG重复次数的微小差异似乎并非风险或侵袭性疾病的有力指标,但这种大小多态性可能是参与前列腺癌的众多遗传和环境风险因素之一。

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