Pagliacci M C, Tognellini R, Grignani F, Nicoletti I
Istituto di Clinica Medica 1, Università di Perugia e Centro Trasfusionale del Policlinico, Italy.
Endocrinology. 1991 Nov;129(5):2555-62. doi: 10.1210/endo-129-5-2555.
Somatostatin (SS) and SS analogs have been shown to exert an antiproliferative effect on several transplantable tumors in animals and to reduce the growth of pancreatic, pituitary, and mammary tumor cells in vitro. We evaluated the effects that the SS analog SMS 201-995 exerts on growth, cell-cycle parameters, and suicidal cell death (apoptosis) of human breast cancer cells (MCF-7) in vitro. SMS 201-995 significantly reduced the MCF-7 cell growth induced by serum, estradiol, insulin, and insulin-like growth Factor-I in both short term and long term experiments. The effect was maximal when 10 nM estradiol was used as mitogen in long term cultures. SMS 201-995 treatment produced a slight but transient accumulation of cells in the G2/M phase but did not cause any noteworthy reduction in the percentage of proliferating cells. There was, instead, a time-related increase in the number of cells with the flow-cytometric characteristics of apoptosis in the cultures treated with the SS analog, which correlated well with its growth-inhibiting activity. It would, therefore, seem that SMS 201-995 exerts its inhibitory effect on MCF-7 cell growth in vitro mainly by enhancing the rate of programmed (or suicidal) cell death in the culture.
生长抑素(SS)及其类似物已被证明对动物体内多种可移植肿瘤具有抗增殖作用,并能在体外抑制胰腺、垂体和乳腺肿瘤细胞的生长。我们评估了生长抑素类似物SMS 201-995在体外对人乳腺癌细胞(MCF-7)的生长、细胞周期参数和自杀性细胞死亡(凋亡)的影响。在短期和长期实验中,SMS 201-995均能显著降低血清、雌二醇、胰岛素和胰岛素样生长因子-I诱导的MCF-7细胞生长。在长期培养中,当使用10 nM雌二醇作为促有丝分裂原时,这种作用最为明显。SMS 201-995处理使细胞在G2/M期出现轻微但短暂的积聚,但并未导致增殖细胞百分比出现任何显著降低。相反,在用生长抑素类似物处理的培养物中,具有凋亡流式细胞术特征的细胞数量随时间增加,这与其生长抑制活性密切相关。因此,SMS 201-995在体外对MCF-7细胞生长的抑制作用似乎主要是通过提高培养物中程序性(或自杀性)细胞死亡的速率来实现的。