Katayose Y, Kim M, Rakkar A N, Li Z, Cowan K H, Seth P
Medicine Branch, Division of Clinical Sciences, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.
Cancer Res. 1997 Dec 15;57(24):5441-5.
p27Kip1, a cyclin-dependent kinase inhibitor, is recognized as a negative regulator of the cell cycle. In this paper, we report that overexpression of p27Kip1 triggers apoptosis in several different human cancer cell lines. Using a recombinant adenoviral vector that expresses p27Kip1 (Adp27), we found that overexpression of p27Kip1 in MDA-MB-231 breast cancer cells induces apoptosis that was seen by a number of different techniques, including flow cytometry and in situ terminal deoxynucleotidyl transferase-mediated nick end labeling, flow cytometric assay for sub-G1 population, and 4',6-diamindino-2-phenylindole staining. Cleavage of poly(ADP-ribose) polymerase and degradation of cyclin B1, events that are known to be associated with apoptosis, were also observed following overexpression of p27Kip1. This is the first report indicating a role for p27Kip1 in induction of apoptosis.
p27Kip1是一种细胞周期蛋白依赖性激酶抑制剂,被认为是细胞周期的负调控因子。在本文中,我们报道p27Kip1的过表达在几种不同的人类癌细胞系中引发凋亡。使用表达p27Kip1的重组腺病毒载体(Adp27),我们发现在MDA-MB-231乳腺癌细胞中p27Kip1的过表达诱导了凋亡,这通过多种不同技术得以观察到,包括流式细胞术、原位末端脱氧核苷酸转移酶介导的缺口末端标记、亚G1期群体的流式细胞术检测以及4',6-二脒基-2-苯基吲哚染色。在p27Kip1过表达后,还观察到聚(ADP-核糖)聚合酶的切割和细胞周期蛋白B1的降解,这些事件已知与凋亡相关。这是首次报道表明p27Kip1在诱导凋亡中发挥作用。