Pettaway C A
Department of Urology, University of Texas MD Anderson Cancer Center, Houston 77030, USA.
J Natl Med Assoc. 1999 Dec;91(12):653-60.
Pathologic and epidemiologic data suggest that while little racial variation exists in prostate cancer prevalence ("autopsy cancer"), striking racial variation exists for the clinically diagnosed form of the disease. A review of the available literature was performed to define whether racial differences in serum androgen levels or qualitative or quantitative differences in the androgen receptor were correlated with prostate cancer incidence or severity. Black men were found to be exposed to higher circulating testosterone levels from birth to about age 35 years. Such differences were not consistently noted among older men. Significant differences also were found for dihydrotestosterone metabolites among black, white, and Asian men. Unique racial genetic polymorphisms were noted for the gene for 5 alpha-reductase type 2 among black and Asian men. Novel androgen receptor mutations recently have been described among Japanese, but not white, men with latent prostate cancer. Finally, androgen receptor gene polymorphisms leading to shorter or longer glutamine and glycine residues in the receptor protein are correlated with racial variation in the incidence and severity of prostate cancer. This same polymorphism also could explain racial variation in serum prostate-specific antigen levels. Collectively, these data strongly suggest racial differences within the androgen/androgen receptor pathway not only exist but could be one cause of clinically observed differences in the biology of prostate cancer among racial groups.
病理和流行病学数据表明,虽然前列腺癌患病率(“尸检癌”)几乎不存在种族差异,但该疾病临床诊断形式存在显著的种族差异。我们对现有文献进行了综述,以确定血清雄激素水平的种族差异或雄激素受体的定性或定量差异是否与前列腺癌的发病率或严重程度相关。研究发现,黑人男性从出生到大约35岁期间循环睾酮水平较高。在老年男性中,这种差异并不一致。在黑人、白人和亚洲男性中,二氢睾酮代谢物也存在显著差异。在黑人和亚洲男性中,发现了2型5α-还原酶基因独特的种族遗传多态性。最近在患有潜伏性前列腺癌的日本男性而非白人男性中描述了新的雄激素受体突变。最后,雄激素受体基因多态性导致受体蛋白中谷氨酰胺和甘氨酸残基变短或变长,这与前列腺癌发病率和严重程度的种族差异相关。这种相同的多态性也可以解释血清前列腺特异性抗原水平的种族差异。总体而言,这些数据有力地表明雄激素/雄激素受体途径内不仅存在种族差异,而且可能是不同种族群体中前列腺癌生物学临床观察差异的一个原因。