Yang Z Y, Perkins N D, Ohno T, Nabel E G, Nabel G J
Howard Hughes Medical Institute, University of Michigan Medical Center, Department of Internal Medicine, Ann Arbor 48109-0650, USA.
Nat Med. 1995 Oct;1(10):1052-6. doi: 10.1038/nm1095-1052.
The p21 gene encodes a cyclin-dependent kinase inhibitor that affects cell-cycle progression, but the potential of this gene product to serve as a tumour suppressor in vivo has not been established. In this report, we show that the growth of malignant cells in vitro and in vivo is inhibited by expression of p21. Expression of p21 resulted in an accumulation of cells in G0/G1, altered morphology, and cell differentiation, but apoptosis was not induced. Introduction of p21 with adenoviral vectors into malignant cells completely suppressed their growth in vivo and also reduced the growth of established pre-existing tumours. Gene transfer of p21 may provide a molecular genetic approach to arresting cancer cell growth by committing malignant cells irreversibly to a pathway of terminal differentiation.
p21基因编码一种细胞周期蛋白依赖性激酶抑制剂,它会影响细胞周期进程,但该基因产物在体内作为肿瘤抑制因子的潜力尚未得到证实。在本报告中,我们表明p21的表达在体外和体内均可抑制恶性细胞的生长。p21的表达导致细胞在G0/G1期积累,形态改变以及细胞分化,但未诱导细胞凋亡。用腺病毒载体将p21导入恶性细胞可完全抑制其在体内的生长,还能使已形成的现有肿瘤的生长减缓。p21的基因转移可能提供一种分子遗传学方法,通过使恶性细胞不可逆地进入终末分化途径来阻止癌细胞生长。