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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Combination of atorvastatin and celecoxib synergistically induces cell cycle arrest and apoptosis in colon cancer cells.
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Combination of atorvastatin and celecoxib synergistically induces cell cycle arrest and apoptosis in colon cancer cells.

机译:阿托伐他汀和塞来昔布的组合可协同诱导结肠癌细胞的细胞周期停滞和凋亡。

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摘要

Previous studies in animal models have shown enhanced efficacy of a combined treatment of statins and Nonsteroidal anti-inflammatory drugs against colorectal cancer development. In our study, we investigated the combinational effects of atorvastatin and celecoxib in 2 human colon cancer cell lines HCT116 and HT29. Celecoxib moderately inhibited the growth of both cell lines with a similar IC(50) of 40-50 microM, whereas atorvastatin showed stronger growth inhibitory effect in HCT116 cells than in HT29 cells (IC(50) of 5-8 microM vs. 30-35 microM) after treatment for 48-72 hr. The combination of these 2 agents produced strong synergistic actions, as determined by isobologram analysis. Flow cytometry analysis indicated that the combination treatment for 24 hr caused extensive cell cycle arrest in G0/G1 phase; whereas at 48 hr or longer, apoptosis was induced significantly. The effects produced by the combination were much stronger than that by atorvastatin or celecoxib alone. Our results further demonstrated that the combinational effects of atorvastatin/celecoxib were associated with increased levels of p21(Cip1/Waf1), p27(Kip1), and phospho-JNK; decreased levels of phospho-AKT and hyper-phosphorylated Rb; and activation of caspase cascade. Atorvastatin/celecoxib combination also selectively modified membrane localization of small G-proteins, such as RhoA, RhoB and RhoC, which may contribute to the anti-cancer effects. Taken together, the results demonstrated a strong synergy between the actions of atorvastatin and celecoxib in growth inhibition and killing of human colon cancer cells. The present work suggests the possible therapeutic application of this combination and provides leads for mechanistic and biomarker investigations in clinical trials.
机译:先前在动物模型中的研究表明,他汀类药物和非甾体类抗炎药联合治疗抗结直肠癌发展的功效增强。在我们的研究中,我们研究了阿托伐他汀和塞来昔布在2种人结肠癌细胞系HCT116和HT29中的联合作用。塞来昔布以40-50 microM的相似IC(50)适度抑制两种细胞系的生长,而阿托伐他汀在HCT116细胞中显示出比HT29细胞更强的生长抑制作用(IC(50)在5-8 microM对30- 35 microM)处理48-72小时后。通过等效线图分析确定,这两种药物的组合产生了强大的协同作用。流式细胞仪分析表明,联合治疗24小时导致G0 / G1期广泛的细胞周期停滞。而在48小时或更长时间,则明显诱导了细胞凋亡。组合产生的作用比单独使用阿托伐他汀或塞来昔布产生的作用要强得多。我们的结果进一步证明,阿托伐他汀/塞来昔布的联合作用与p21(Cip1 / Waf1),p27(Kip1)和磷酸化JNK水平升高有关。磷酸-AKT和超磷酸化Rb水平降低;和半胱天冬酶级联反应的激活阿托伐他汀/塞来昔布的组合还选择性地修饰了小G蛋白(例如RhoA,RhoB和RhoC)的膜定位,这可能有助于抗癌作用。两者合计,结果证明了阿托伐他汀和塞来昔布在抑制人类结肠癌细胞的生长和杀死中的作用之间有很强的协同作用。目前的工作表明这种组合的可能的治疗应用,并为临床试验中的机制和生物标志物研究提供线索。

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