Department of Clinical Sciences, Molecular Genetic Reproductive Medicine, Lund University, Malmö, Sweden.
Reprod Toxicol. 2013 Jan;35:144-9. doi: 10.1016/j.reprotox.2012.10.010. Epub 2012 Oct 29.
Increased incidence of prostate cancer has been reported in men exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). TCDD acts through the aryl hydrocarbon receptor (AhR), which interacts with the androgen receptor (AR). The AR gene contains a polymorphic CAG repeat that influences its transcriptional activity. We investigated the influence of TCDD on prostate cancer cells (PC-3) and non-tumor prostate cells (PNT1A) on 5α-dihydrotestosterone-activated ARs containing CAG repeats within normal length range (16, 22, and 28). The AhR target gene CYP1A1 mRNA expression was induced by TCDD, but was not affected by the AR CAG length. TCDD had no effect on AR activity in PC-3 cells, whereas the shortest AR variant was induced by TCDD in PNT1A cells. In conclusion, the CAG length dependent effect of TCDD on AR activity in PNT1A, but not in PC-3 cells, indicates as a cell-specific effect of TCDD on AR activity.
据报道,接触 2,3,7,8-四氯二苯并对二恶英(TCDD)的男性中前列腺癌的发病率增加。TCDD 通过芳烃受体(AhR)起作用,AhR 与雄激素受体(AR)相互作用。AR 基因含有影响其转录活性的多态性 CAG 重复。我们研究了 TCDD 对包含正常长度范围内(16、22 和 28)CAG 重复的 5α-二氢睾酮激活的 AR 的前列腺癌细胞(PC-3)和非肿瘤前列腺细胞(PNT1A)的影响。TCDD 诱导 AhR 靶基因 CYP1A1 mRNA 的表达,但不受 AR CAG 长度的影响。TCDD 对 PC-3 细胞中的 AR 活性没有影响,而在 PNT1A 细胞中,最短的 AR 变体被 TCDD 诱导。总之,TCDD 在 PNT1A 细胞中对 AR 活性的 CAG 长度依赖性影响,但在 PC-3 细胞中没有,表明 TCDD 对 AR 活性具有细胞特异性影响。