Wainstein M A, He F, Robinson D, Kung H J, Schwartz S, Giaconia J M, Edgehouse N L, Pretlow T P, Bodner D R, Kursh E D
Department of Urology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
Cancer Res. 1994 Dec 1;54(23):6049-52.
The long-term propagation of primary human prostate cancer (PCA) in vivo or in vitro has been rare. Most such PCAs are phenotypically different from most PCAs in humans; i.e., they make little prostate specific antigen and respond little, if at all, to androgen deprivation. A serially transplantable, primary human PCA, designated CWR22, exhibits a clonal cytogenetic aberration, causes high elevations of prostate specific antigen in the peripheral blood of nude mice, and is unusually responsive to androgen deprivation as compared with other xenografts. Studies of mRNA from CWR22 have demonstrated the expression of prostate specific antigen and the epidermal growth factor receptor family including erbB1/epidermal growth factor receptor, erbB2/neu, and erbB3, but not erbB4. A ligand for these receptors, the neu differentiation factor, is also expressed.
原发性人类前列腺癌(PCA)在体内或体外的长期传代一直很少见。大多数此类PCA在表型上与人类大多数PCA不同;即,它们产生的前列腺特异性抗原很少,并且对雄激素剥夺几乎没有反应(如果有反应的话)。一种可连续移植的原发性人类PCA,命名为CWR22,表现出克隆性细胞遗传学异常,在裸鼠外周血中导致前列腺特异性抗原高度升高,并且与其他异种移植相比,对雄激素剥夺异常敏感。对CWR22的mRNA研究表明,其表达前列腺特异性抗原以及表皮生长因子受体家族,包括erbB1/表皮生长因子受体、erbB2/neu和erbB3,但不包括erbB4。这些受体的一种配体,即neu分化因子,也有表达。