Goyer Robert A, Liu Jie, Waalkes Michael P
NCI at NIEHS, Research Triangle Park, NC 27709, USA.
Biometals. 2004 Oct;17(5):555-8. doi: 10.1023/b:biom.0000045738.59708.20.
Cancer of the prostate is an important and potentially fatal disease in humans but the etiology is yet undefined. Cadmium and cadmium compounds are known to be human carcinogens based on findings of increased risk to lung cancer among exposed workers, but a relationship between cancer of the prostate and/or testis in humans is unclear in spite of suggestive results in rats. Parenteral administration or oral exposure to cadmium can result in proliferate lesions and tumors of the prostate in rats. The ability of cadmium to produce neoplasms in the prostate of rats is atypically dose-related and only occurs in rats at doses below the threshold for significant testicular toxicity. Testicular androgen production is essential for the maintenance of the prostate and prostate tumors. The rat testis may also develop tumors if cadmium is given parenterally at high doses. Subsequent to testicular hemorrhagic necrosis, there will be loss of testosterone production and hyperplasia and neoplasia of testicular interstitial cells, thought to be a response to trophic hormone release from the pituitary. The pathogenesis of prostatic cadmium carcinogenesis might include aberrant gene expression resulting in stimulation of cell proliferation or blockage of apoptosis. Activation of transcription factors such as the metallothionein gene and activation of some protooncogenes may enhance cell proliferation with damaged DNA. Suppression of DNA repair would add to the population of cells with damaged DNA. Chemically induced apoptosis can be blocked by cadmium, facilitating aberrant cell accumulation.
前列腺癌是人类一种重要的潜在致命疾病,但其病因尚未明确。基于对接触镉的工人肺癌风险增加的研究结果,镉及其化合物被认为是人类致癌物,然而,尽管在大鼠身上有提示性结果,但镉与人类前列腺癌和/或睾丸癌之间的关系仍不明确。给大鼠腹腔注射或经口暴露于镉可导致前列腺增生性病变和肿瘤。镉在大鼠前列腺中产生肿瘤的能力与剂量的关系不典型,且仅在低于显著睾丸毒性阈值的剂量下才会在大鼠中出现。睾丸雄激素的产生对于维持前列腺和前列腺肿瘤至关重要。如果给大鼠腹腔注射高剂量镉,大鼠睾丸也可能发生肿瘤。在睾丸出血性坏死之后,睾酮的产生会减少,睾丸间质细胞会增生和形成肿瘤,这被认为是对垂体释放的促激素的一种反应。前列腺镉致癌的发病机制可能包括异常基因表达导致细胞增殖刺激或细胞凋亡受阻。金属硫蛋白基因等转录因子的激活以及一些原癌基因的激活可能会在DNA受损的情况下增强细胞增殖。DNA修复的抑制会增加DNA受损细胞的数量。镉可阻断化学诱导的细胞凋亡,促进异常细胞的积累。