Said Mahmoud M, Hokaiwado Naomi, Tang Mingxi, Ogawa Kumiko, Suzuki Shugo, Ghanem Hala M, Esmat Amr Y, Asamoto Makoto, Refaie Fawzia M, Shirai Tomoyuki
Department of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya, 467-8601, Japan.
Cancer Sci. 2006 Jun;97(6):459-67. doi: 10.1111/j.1349-7006.2006.00213.x.
The effects of leuprorelin acetate, a luteinizing hormone-releasing hormone agonist (LHRH-A), on prostate carcinogenesis in probasin/SV40 Tag transgenic rat was investigated. Fifteen weeks after administration of 0.28 and 2.8 mg/kg leuprorelin, prostate weights and serum testosterone levels were significantly decreased compared to values for transgenic controls. Histopathological findings revealed that the incidence of prostatic adenocarcinomas was significantly reduced in ventral, dorsal and lateral lobes of the prostate, correlating with decreased expression of SV40 Tag oncoprotein as well as inhibition of DNA synthesis and proliferation of epithelial cells in neoplastic lesions of the ventral prostate. Microarray analysis further showed leuprorelin acetate to significantly inhibit testicular steroidogenesis, suppressing the expression of SV40 Tag oncoprotein and altering the expression of a large number of genes which might be involved in the inhibition of prostate cancer progression in this rat model.
研究了促黄体激素释放激素激动剂(LHRH-A)醋酸亮丙瑞林对前列腺素/SV40 Tag转基因大鼠前列腺癌发生的影响。给予0.28和2.8mg/kg醋酸亮丙瑞林15周后,与转基因对照组相比,前列腺重量和血清睾酮水平显著降低。组织病理学结果显示,前列腺腹侧、背侧和外侧叶前列腺腺癌的发生率显著降低,这与SV40 Tag癌蛋白表达降低以及腹侧前列腺肿瘤性病变中上皮细胞DNA合成和增殖的抑制相关。微阵列分析进一步表明,醋酸亮丙瑞林可显著抑制睾丸类固醇生成,抑制SV40 Tag癌蛋白的表达,并改变大量可能参与该大鼠模型前列腺癌进展抑制的基因的表达。