Beleva Elina, Diukendjieva Antonia, Pajeva Ilza, Tsakovska Ivanka
QSAR and Molecular Modelling, Institute of Biophysics and Biomedical Engineering, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Clinic of Hematology, Military Medical Academy, Sofia, Bulgaria.
JMIR Res Protoc. 2025 Jun 5;14:e66197. doi: 10.2196/66197.
Drug efflux mediated by transporter proteins is one of the major mechanisms conferring multidrug resistance (MDR) to antimicrobial agents in bacteria and to chemotherapeutics in cancer cells. Therefore, the development or identification of efflux modulators represents a promising strategy to overcome the resistant phenotype. Various chemical compounds have been tested in experimental studies as reversal agents either in combination with antimicrobial or anticancer drugs and have shown sensitizing activity in resistant bacteria or cancer cell lines. Owing to the common resistance mechanisms exhibited by bacteria and cancer cells, the identification of chemical agents with dual reversal activity offers a strategy to simultaneously combat antibacterial and cancer multidrug resistance.
This study aims to conduct a systematic review to identify compounds that have shown activity in reversing antibacterial as well as cancer MDR mediated by drug efflux pumps and to summarize their structural and biological parameters responsible for the interactions with drug efflux pumps.
The protocol has been developed in accordance with PRISMA-P (Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols) guidelines. We searched PubMed and Scopus databases for abstracts of full-text peer-reviewed journal papers in English language published between January 2012 and September 2024. Only studies from in vitro experiments were considered if they used methods to detect changes in antibiotic sensitivity of resistant bacteria and chemosensitivity of resistant cancer cells upon treatment with efflux pump inhibitors. A total of 763 unique records were identified. Of them, 246 were selected for full-text review based on the eligibility criteria. Abstract screening was performed by 2 independent reviewers. As of March 1, 2025, the systematic review is at the stage of completed abstract screening. The next steps of the full-text review, study selection, data extraction, and risk of bias assessment will be performed by 2 independent reviewers as well. Main data elements will include a structural identifier of the tested inhibitor, bacterial strain, cancer cell line, methods proving reversal activity, half maximal inhibitory concentration, and other relevant quantitative estimates of reversal activity. Data synthesis will be performed as a narrative summary and the content will be curated in tabular and graphical form.
We anticipate that results from this study will outline the potential of various compounds to act as dual chemosensitizers and reverse both antimicrobial and cancer MDR.
Our review will highlight the overlap between efflux pumps' inhibition as a strategy to combat MDR in both bacterial and cancer cells and it will provide structured data for rational drug design of dual efflux pump inhibitors.
PROSPERO CRD42024548350; https://www.crd.york.ac.uk/PROSPERO/view/CRD42024548350.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/66197.
转运蛋白介导的药物外排是细菌对抗菌药物以及癌细胞对化疗药物产生多药耐药性(MDR)的主要机制之一。因此,开发或鉴定外排调节剂是克服耐药表型的一种有前景的策略。在实验研究中,各种化合物已作为逆转剂与抗菌或抗癌药物联合进行测试,并在耐药细菌或癌细胞系中显示出增敏活性。由于细菌和癌细胞表现出共同的耐药机制,鉴定具有双重逆转活性的化学试剂为同时对抗细菌和癌症多药耐药性提供了一种策略。
本研究旨在进行系统综述,以鉴定在逆转由药物外排泵介导的抗菌及癌症多药耐药性方面具有活性的化合物,并总结其与药物外排泵相互作用的结构和生物学参数。
该方案已按照PRISMA-P(系统评价和Meta分析方案的首选报告项目)指南制定。我们在PubMed和Scopus数据库中搜索了2012年1月至2024年9月期间以英文发表的全文同行评审期刊论文的摘要。仅考虑来自体外实验的研究,前提是这些研究使用方法检测外排泵抑制剂处理后耐药细菌的抗生素敏感性和耐药癌细胞的化学敏感性变化。共识别出763条独特记录。其中,根据纳入标准选择了246条进行全文评审。摘要筛选由2名独立评审员进行。截至2025年3月1日,系统综述处于完成摘要筛选阶段。全文评审、研究选择、数据提取和偏倚风险评估的后续步骤也将由2名独立评审员进行。主要数据元素将包括受试抑制剂的结构标识符、细菌菌株、癌细胞系、证明逆转活性的方法、半数最大抑制浓度以及逆转活性的其他相关定量估计。数据合成将以叙述性总结形式进行,内容将整理成表格和图形形式。
我们预计本研究结果将概述各种化合物作为双重化学增敏剂并逆转抗菌和癌症多药耐药性的潜力。
我们的综述将突出抑制外排泵作为对抗细菌和癌细胞多药耐药性策略之间的重叠,并将为双重外排泵抑制剂的合理药物设计提供结构化数据。
PROSPERO CRD42024548350;https://www.crd.york.ac.uk/PROSPERO/view/CRD42024548350。
国际注册报告标识符(IRRID):PRR1-10.2196/66197。