Gorospe M, Wang X, Guyton K Z, Holbrook N J
Laboratory of Cellular and Molecular Biology, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Mol Cell Biol. 1996 Dec;16(12):6654-60. doi: 10.1128/MCB.16.12.6654.
Prostaglandin A2 (PGA2) suppresses tumor growth in vivo, is potently antiproliferative in vitro, and is a model drug for the study of the mammalian stress response. Our previous studies using breast carcinoma MCF-7 cells suggested that p21(Waf1/Cip1) induction enabled cells to survive PGA2 exposure. Indeed, the marked sensitivity of human colorectal carcinoma RKO cells to the cytotoxicity of PGA2 is known to be associated with a lack of a PGA2-mediated increase in p21(Waf1/Cip1) expression, inhibition of cyclin-dependent kinase activity, and growth arrest. To determine if cell death following exposure to PGA2 could be prevented by forcing the expression of p21(Waf1/Cip1) in RKO cells, we utilized an adenoviral vector-based expression system. We demonstrate that ectopic expression of p21(Waf1/Cip1) largely rescued RKO cells from PGA2-induced apoptotic cell death, directly implicating p21(Waf1/Cip1) as a determinant of the cellular outcome (survival versus death) following exposure to PGA2. To discern whether p21(Waf1/Cip1)-mediated protection operates through the implementation of cellular growth arrest, other growth-inhibitory treatments were studied for the ability to attenuate PGA2-induced cell death. Neither serum depletion nor suramin (a growth factor receptor antagonist) protected RKO cells against PGA2 cytotoxicity, and neither induced p21(Waf1/Cip1) expression. Mimosine, however, enhanced p21(Waf1/Cip1) expression, completely inhibited RKO cell proliferation, and exerted marked protection against a subsequent PGA2 challenge. Taken together, our results directly demonstrate a protective role for p21(Waf1/Cip1) during PGA2 cellular stress and provide strong evidence that the implementation of cellular growth arrest contributes to this protective influence.
前列腺素A2(PGA2)在体内可抑制肿瘤生长,在体外具有强大的抗增殖作用,是研究哺乳动物应激反应的模型药物。我们之前使用乳腺癌MCF - 7细胞进行的研究表明,p21(Waf1/Cip1)的诱导使细胞能够在PGA2暴露下存活。实际上,已知人结肠直肠癌RKO细胞对PGA2细胞毒性的显著敏感性与缺乏PGA2介导的p21(Waf1/Cip1)表达增加、细胞周期蛋白依赖性激酶活性抑制和生长停滞有关。为了确定通过在RKO细胞中强制表达p21(Waf1/Cip1)是否可以预防暴露于PGA2后的细胞死亡,我们利用了基于腺病毒载体的表达系统。我们证明,p21(Waf1/Cip1)的异位表达在很大程度上使RKO细胞免受PGA2诱导的凋亡性细胞死亡,直接表明p21(Waf1/Cip1)是暴露于PGA2后细胞结局(存活与死亡)的决定因素。为了辨别p21(Waf1/Cip1)介导的保护是否通过细胞生长停滞的实现来发挥作用,我们研究了其他生长抑制处理减轻PGA2诱导的细胞死亡的能力。血清饥饿和苏拉明(一种生长因子受体拮抗剂)均不能保护RKO细胞免受PGA2细胞毒性,且两者均未诱导p21(Waf1/Cip1)表达。然而,含羞草碱可增强p21(Waf1/Cip1)表达,完全抑制RKO细胞增殖,并对随后的PGA2攻击发挥显著保护作用。综上所述,我们的结果直接证明了p21(Waf1/Cip1)在PGA2细胞应激期间的保护作用,并提供了有力证据表明细胞生长停滞的实现有助于这种保护作用。