Lotan R, Giotta G, Nork E, Nicolson G L
J Natl Cancer Inst. 1978 May;60(5):1035-41. doi: 10.1093/jnci/60.5.1035.
The in vitro proliferation of murine melanoma cell lines S91 and B16 was inhibited by retinoic acid and retinyl acetate. The inhibitory effects were dependent on retinoid concentration and increased from 55 and 30% at 10(-9) M retinoic acid to 85 and 82% at 10(-5) M retinoic acid for S91 and B16 melanoma cells, respectively. S91 melanoma cells were more sensitive than B16 melanoma cells to inhibition by either retinoid, and both cell lines were more sensitive to retinoic acid than to retinyl acetate. When exposed to 10(-5) M retinoic acid, the two cell types grew at the same rate as did control cells for 48 hours, whereupon the growth rates of retinoid-treated cells decreased. After 6 days, the number of cells in control cultures increased 140 times (S91 melanoma cells) and 265 times (B16 melanoma cells), whereas retinoic acid-treated cells increased only 14 times (S91 melanoma cells) and 40 times (B16 melanoma cells). The degree of growth inhibition by retinoic acid was not dependent on initial cell density. Cortisone and hydrocortisone failed to prevent or reduce the inhibitory effect of retinoic acid; the release of lysosomal acid phosphatase was not increased and the intracellular level of 3',5'-cyclic AMP in cells grown for 5 days in the presence of 10(-5) M retinoic acid was not elevated. Viability of S91 and B16 cells after 8 days' exposure to 10(-5) M retinoic acid was similar to that in control cultures. The reduced growth rate of retinoic acid-treated cells reversed to the control rate 48-72 hours after removal of retinoic acid from the growth medium.
维甲酸和醋酸视黄酯可抑制小鼠黑色素瘤细胞系S91和B16的体外增殖。抑制作用取决于类维生素A的浓度,对于S91和B16黑色素瘤细胞,抑制率分别从10⁻⁹ M维甲酸时的55%和30%增加到10⁻⁵ M维甲酸时的85%和82%。S91黑色素瘤细胞比B16黑色素瘤细胞对任何一种类维生素A的抑制作用都更敏感,并且两种细胞系对维甲酸的敏感性都高于醋酸视黄酯。当暴露于10⁻⁵ M维甲酸时,两种细胞类型在48小时内的生长速率与对照细胞相同,此后类维生素A处理的细胞生长速率下降。6天后,对照培养物中的细胞数量增加了140倍(S91黑色素瘤细胞)和265倍(B16黑色素瘤细胞),而维甲酸处理的细胞仅增加了14倍(S91黑色素瘤细胞)和40倍(B16黑色素瘤细胞)。维甲酸的生长抑制程度不依赖于初始细胞密度。可的松和氢化可的松未能预防或降低维甲酸的抑制作用;溶酶体酸性磷酸酶的释放没有增加,并且在10⁻⁵ M维甲酸存在下培养5天的细胞中3',5'-环磷酸腺苷的细胞内水平没有升高。暴露于10⁻⁵ M维甲酸8天后,S91和B16细胞的活力与对照培养物中的相似。从生长培养基中去除维甲酸后48 - 72小时,维甲酸处理的细胞降低的生长速率恢复到对照速率。