Ramipril, perindopril and trandolapril as potential chemosensitizers in ovarian cancer: Considerations for drug repurposing

IF 7.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Discovery Today Pub Date : 2025-04-01 Epub Date: 2025-03-13 DOI:10.1016/j.drudis.2025.104331
Katarzyna Regulska , Paulina Gieremek , Marcin Michalak , Tomasz Kolenda , Marlena Janiczek-Polewska , Joanna Kozłowska-Masłoń , Zefiryn Cybulski , Beata J. Stanisz
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Abstract

Ovarian cancer (OC) has poor survival statistics and increasing prevalence. One of the new options for its therapy could be overcoming platinum resistance. In this review, we have considered the idea of repositioning angiotensin-converting enzyme inhibitors (ACE-Is) as chemosensitizers. These drugs have been shown to suppress angiogenesis and OC cell migration in preclinical studies. Moreover, clinical data have shown that using ACE-Is with standard chemotherapy prolongs patient survival. Based on this rationale, we discuss the available in vitro models of OC for future studies with ACE-Is and demonstrate an in silico approach that has enabled us to select the most promising molecules: perindopril, ramipril, trandolapril and their diketopiperazine derivatives.

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雷米普利、培哚普利和曲多普利作为卵巢癌的潜在化学增敏剂:药物再利用的考虑。
卵巢癌(OC)有较差的生存统计数据和不断增加的患病率。该疗法的新选择之一可能是克服铂耐药性。在这篇综述中,我们考虑了重新定位血管紧张素转换酶抑制剂(ACE-Is)作为化学增敏剂的想法。在临床前研究中,这些药物已被证明可以抑制血管生成和OC细胞的迁移。此外,临床数据表明,ACE-Is与标准化疗联合使用可延长患者生存期。基于这一基本原理,我们讨论了未来ACE-Is研究中可用的体外OC模型,并展示了一种计算机方法,使我们能够选择最有希望的分子:培哚普利、雷米普利、曲多拉普利及其双酮哌嗪衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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