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ABT-737与匹他替尼协同增强匹伐他汀诱导的卵巢癌细胞凋亡。

ABT-737 and pictilisib synergistically enhance pitavastatin-induced apoptosis in ovarian cancer cells.

作者信息

De Wolf Elizabeth, De Wolf Christopher, Richardson Alan

机构信息

Institute for Science and Technology in Medicine, Guy Hilton Research Centre, Stoke-on-Trent ST4 7QB, UK.

School of Pharmacy, Keele University, Stoke-on-Trent ST5 5BG, UK.

出版信息

Oncol Lett. 2018 Feb;15(2):1979-1984. doi: 10.3892/ol.2017.7516. Epub 2017 Dec 5.

DOI:10.3892/ol.2017.7516
PMID:29434898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5778268/
Abstract

There is considerable interest in redeploying drugs for use in combination with other oncology therapeutics. The single-agent activity of statins in ovarian cancer has been widely reported, however the drug concentration required to cause cell death is considerably higher than that achieved in patients receiving statin treatment for hypercholesterolemia. Unfortunately, statins can cause myopathy when administered in high doses. One solution to this is to identify drugs that could be used in combination with statins to reduce the dose required and those that may potentially reduce the incidence of adverse side effects. When the BH3 mimetic ABT-737, or the phosphatidylinositol 3-kinase inhibitor pictilisib, were combined with pitavastatin in cell growth assays using Ovcar-3 and Igrov-1 cells, the drug combinations were more effective than pitavastatin alone. In support of this, ABT-737 or pictilisib markedly increased cell death induced by pitavastatin in several ovarian cancer cell lines. The drugs were also synergistic in apoptosis assays. These observations suggested that either BH3 mimetics or pictilisib in combination with pitavastatin could be used in a subset of ovarian tumours, particularly those sensitive to BH3 mimetics, and phosphatase and tensin homolog inhibition, in the treatment of ovarian cancer.

摘要

人们对重新调配药物以与其他肿瘤治疗方法联合使用有着浓厚的兴趣。他汀类药物在卵巢癌中的单药活性已被广泛报道,然而,导致细胞死亡所需的药物浓度远高于接受他汀类药物治疗高胆固醇血症的患者所达到的浓度。不幸的是,高剂量使用他汀类药物会导致肌病。解决这一问题的一个办法是确定可与他汀类药物联合使用以降低所需剂量的药物,以及那些可能降低不良反应发生率的药物。当BH3模拟物ABT - 737或磷脂酰肌醇3激酶抑制剂匹地西利与匹伐他汀在使用Ovcar - 3和Igrov - 1细胞的细胞生长试验中联合使用时,药物组合比单独使用匹伐他汀更有效。支持这一点的是,ABT - 737或匹地西利在几种卵巢癌细胞系中显著增加了匹伐他汀诱导的细胞死亡。这些药物在凋亡试验中也具有协同作用。这些观察结果表明,BH3模拟物或匹地西利与匹伐他汀联合使用可用于一部分卵巢肿瘤,特别是那些对BH3模拟物、磷酸酶和张力蛋白同源物抑制敏感的肿瘤,用于治疗卵巢癌。

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本文引用的文献

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Dietary geranylgeraniol can limit the activity of pitavastatin as a potential treatment for drug-resistant ovarian cancer.饮食中的香叶基香叶醇可限制匹伐他汀的活性,作为治疗耐药性卵巢癌的一种潜在方法。
Sci Rep. 2017 Jul 14;7(1):5410. doi: 10.1038/s41598-017-05595-4.
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Antagonism of Bcl-XL is necessary for synergy between carboplatin and BH3 mimetics in ovarian cancer cells.在卵巢癌细胞中,Bcl-XL的拮抗作用是卡铂与BH3模拟物协同作用所必需的。
J Ovarian Res. 2016 Apr 14;9:25. doi: 10.1186/s13048-016-0234-y.
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The BH3 Mimetic Obatoclax Accumulates in Lysosomes and Causes Their Alkalinization.BH3模拟物奥巴托克斯在溶酶体中积累并导致其碱化。
PLoS One. 2016 Mar 7;11(3):e0150696. doi: 10.1371/journal.pone.0150696. eCollection 2016.
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Regulation of Mcl-1 by constitutive activation of NF-κB contributes to cell viability in human esophageal squamous cell carcinoma cells.NF-κB 的组成性激活对人食管鳞状细胞癌细胞中 Mcl-1 的调节有助于细胞存活。
BMC Cancer. 2014 Feb 17;14:98. doi: 10.1186/1471-2407-14-98.
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