Lointier P, Wildrick D M, Boman B M
Section of Gastrointestinal Oncology and Digestive Diseases, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Anticancer Res. 1992 Jul-Aug;12(4):1327-30.
Estrogen analogues, moxestrol (10(-8)-10(-5) M) and ethinyl estradiol (10(-8)-10(-6) M), produced a 30% and 15% inhibition of LoVo cell growth, respectively, in serum-free Ham's F-10 medium. Under the same conditions, no growth effects were observed on these cells following the addition of progesterone or testosterone (10(-8)-10(-6) M); however, metribolone (10(-8)-10(-6) M), a synthetic androgen with glucocorticoid receptor-binding properties, moderately stimulated cell growth (18%). The synthetic antiandrogen, RU 23908 (10(-6) M), did not reduce metribolone effects, and hydrocortisone (10(-9)-10(-7) M) stimulated LoVo cell growth by 31% in serum-free medium. In medium containing 10% charcoal-treated fetal bovine serum, the inhibitory effects of estrogens were not observed, and the lower concentrations (10(-11) M) of moxestrol and ethinyl estradiol facilitated cell growth (10 to 15%). The other steroid hormones produced the same results as observed with serum-free medium. These data suggest that estrogen and glucocorticoid hormones may play an important role in the growth of colon carcinoma cells. Androgen and progesterone hormones appear to be less significant in this regard. Serum factors alter the effects of estrogen, but not of glucocorticoids.
雌激素类似物莫昔司琼(10⁻⁸ - 10⁻⁵ M)和炔雌醇(10⁻⁸ - 10⁻⁶ M)在无血清的哈姆氏F - 10培养基中分别对LoVo细胞生长产生了30%和15%的抑制作用。在相同条件下,添加孕酮或睾酮(10⁻⁸ - 10⁻⁶ M)后未观察到对这些细胞的生长影响;然而,美替勃龙(10⁻⁸ - 10⁻⁶ M),一种具有糖皮质激素受体结合特性的合成雄激素,适度刺激了细胞生长(18%)。合成抗雄激素RU 23908(10⁻⁶ M)并未降低美替勃龙的作用,并且氢化可的松(10⁻⁹ - 10⁻⁷ M)在无血清培养基中使LoVo细胞生长增加了31%。在含有10%经活性炭处理的胎牛血清的培养基中,未观察到雌激素的抑制作用,并且较低浓度(10⁻¹¹ M)的莫昔司琼和炔雌醇促进了细胞生长(10%至15%)。其他甾体激素产生了与无血清培养基中观察到的相同结果。这些数据表明雌激素和糖皮质激素可能在结肠癌细胞的生长中起重要作用。雄激素和孕酮激素在这方面似乎不太重要。血清因子改变了雌激素的作用,但未改变糖皮质激素的作用。