Yang Q, Shan L, Segawa N, Nakamura M, Nakamura Y, Mori I, Sakurai T, Kakudo K
Second Department of Pathology, Wakayama Medical College, 811-1 Kimiidera, Wakayama City 641-0012, Japan.
Anticancer Res. 2001 Jan-Feb;21(1A):197-200.
Prostate-specific antigen (PSA) is now used widely for the diagnosis and monitoring of patients with prostate cancer. The PSA gene is a target of the androgen receptor (AR) which interacts with androgen response elements (AREs) in the PSA gene promoter. Recently, we identified two novel polymorphisms in the PSA promoter ARE2 region in breast cancer. We hypothesized that some genetic variations might also exist in the AREs of prostate cancer, and that feature might correlate with cancer development and/or progression. To test this hypothesis, three AREs of the PSA gene promoter were characterized for 47 prostate cancer cases and 105 controls from the Japanese population. We demonstrated the presence of two polymorphisms at positions -252 (G or A) and -205 (A or AA), which were the same as those we have found in breast cancer. Interestingly, the -252 A was linked with the presence of -205 AA, and the -252 G was always linked with the presence of -205 A. Therefore, only A-AA and G-A (-252--205) alleles were present in the Japanese population. The proportion of patients who were either heterozygotes or homozygotes for the A-AA allele was not significantly different from that observed among 105 individuals without cancer (p = 0.726). However, comparing with G-A allele homozygotes, prostate cancer patients carrying at least 1 A-AA alleles tended to exhibit high serum PSA levels (p = 0.0002), poor differentiation (p = 0.0149) and advanced clinical stage (p = 0.0077). These results suggest that the novel polymorphisms identified in the PSA gene promoter may affect transcriptional activity of the PSA gene, and an excess of PSA production may enhance rapid progression of prostate cancer.
前列腺特异性抗原(PSA)目前被广泛用于前列腺癌患者的诊断和监测。PSA基因是雄激素受体(AR)的作用靶点,雄激素受体与PSA基因启动子中的雄激素反应元件(AREs)相互作用。最近,我们在乳腺癌的PSA启动子ARE2区域发现了两种新的多态性。我们推测前列腺癌的AREs中可能也存在一些基因变异,并且这种特征可能与癌症的发生和/或进展相关。为了验证这一假设,我们对来自日本人群的47例前列腺癌病例和105例对照的PSA基因启动子的三个AREs进行了特征分析。我们证实了在-252(G或A)和-205(A或AA)位置存在两种多态性,这与我们在乳腺癌中发现的相同。有趣的是,-252 A与-205 AA的存在相关联,而-252 G总是与-205 A的存在相关联。因此,日本人群中仅存在A-AA和G-A(-252--205)等位基因。A-AA等位基因杂合子或纯合子患者的比例与105例无癌个体中观察到的比例无显著差异(p = 0.726)。然而,与G-A等位基因纯合子相比,携带至少1个A-AA等位基因的前列腺癌患者往往表现出高血清PSA水平(p = 0.0002)、低分化(p = 0.0149)和晚期临床分期(p = 0.0077)。这些结果表明,在PSA基因启动子中鉴定出的新多态性可能影响PSA基因的转录活性,并且过量的PSA产生可能促进前列腺癌的快速进展。