Valette A, Gas N, Jozan S, Roubinet F, Dupont M A, Bayard F
Cancer Res. 1987 Mar 15;47(6):1615-20.
Exposure of MCF-7 human mammary carcinoma cells to 12-O-tetradecanoylphorbol-13-acetate (TPA) results in changes in cell morphology and arrest of cell growth. The inhibition of cell proliferation and the increase in cell volume are concentration dependent; these effects are reversible upon removal of the tumor promoting agent. Electron microscopic studies reveal that TPA increases endoplasmic reticulum and induces the appearance of secretory granules. MCF-7 cells treated by TPA therefore present morphological characteristics of secretory cells. These effects of TPA on MCF-7 cells are accompanied by specific disruption of cell cycle events, a block of cells in G1 at the expense of S base, and a delayed passage through G2. Studies in which a cell cycle lock in G1 is produced by tamoxifen show that exposure of such cells to PA produces cell morphological changes and an inability to progress through the cell cycle when estradiol is added.
MCF-7人乳腺癌细胞暴露于12-O-十四酰佛波醇-13-乙酸酯(TPA)会导致细胞形态改变和细胞生长停滞。细胞增殖的抑制和细胞体积的增加呈浓度依赖性;去除肿瘤促进剂后,这些效应是可逆的。电子显微镜研究表明,TPA会增加内质网并诱导分泌颗粒的出现。因此,经TPA处理的MCF-7细胞呈现出分泌细胞的形态特征。TPA对MCF-7细胞的这些效应伴随着细胞周期事件的特异性破坏,细胞在G1期阻滞,以牺牲S期为代价,并且通过G2期的过程延迟。用他莫昔芬使细胞周期锁定在G1期的研究表明,当添加雌二醇时,将此类细胞暴露于TPA会产生细胞形态变化以及无法通过细胞周期。