Chopra D P, Sarkar F H, Grignon D J, Sakr W A, Mohamed A, Waghray A
Institute of Chemical Toxicology, Karmanos Cancer Institute, Detroit, Michigan 48201, USA.
Cancer Res. 1997 Sep 1;57(17):3688-92.
Research into molecular and cellular defects underlying prostate cancer would be advanced by in vitro models of prostate tumor cells representing patient tumors. We have propagated, in serum-free medium, epithelial cell cultures derived from nondiploid prostate tumors and normal human prostate. The serial passage tumor cells exhibited nondiploid karyotype and transformed phenotypes of focus formation and anchorage-independent growth. In contrast, the normal prostate cells showed diploid karyotype and lacked transformed phenotypes. Both the tumor and normal cells were positive for prostate-specific antigen and cytokeratins 18 and 19 and negative for keratin 15. These results demonstrate that the nondiploid prostate tumors and normal prostate epithelial cell cultures retained their respective in vivo properties and should allow studies to elucidate molecular alterations involved in human prostate cancer.
通过代表患者肿瘤的前列腺肿瘤细胞体外模型,对前列腺癌潜在的分子和细胞缺陷的研究将得到推进。我们在无血清培养基中培养了源自非二倍体前列腺肿瘤和正常人前列腺的上皮细胞。连续传代的肿瘤细胞表现出非二倍体核型以及集落形成和不依赖贴壁生长的转化表型。相比之下,正常前列腺细胞显示二倍体核型且缺乏转化表型。肿瘤细胞和正常细胞的前列腺特异性抗原、细胞角蛋白18和19均呈阳性,而角蛋白15呈阴性。这些结果表明,非二倍体前列腺肿瘤和正常前列腺上皮细胞培养物保留了它们各自的体内特性,应该能够用于阐明人类前列腺癌相关分子改变的研究。