Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States.
Department of Microbiology and Immunology, Lewis Katz School of Medicine, Temple University, 3400 North Broad Street, Philadelphia, PA 19140, United States.
Recent Pat Anticancer Drug Discov. 2021;16(2):136-160. doi: 10.2174/1574892816666210208232251.
Cancer is a multistep process involving genetic and epigenetic changes in the somatic genome. Genetic mutations as well as environmental factors lead to the initiation, promotion, and progression of cancer. Metastasis allows cancer cells to spread via circulatory and lymphatic systems; secondary tumorigenesis typically leads to a fatal outcome. Recent experimental evidence suggests that Cancer Stem Cells (CSCs) play a pivotal role in tumor progression. A tumor is heterogeneous and composed of different cell types. CSCs are a subpopulation of tumor cells possessing abilities to self-renew and differentiate.
The aim of this study was to present repurposed drugs, and potential candidates, that can serve as anticancer medications intended to target resistant cancer cells, i.e. CSCs.
Research publications, FDA filings, and patents have been reviewed for repurposed drugs or drug combinations that can act to improve cancer treatment and care.
Drugs that act against CSCs include ones approved for treatment of diabetes (metformin & thiazolidinediones), parasitic diseases (chloroquine, niclosamide, mebendazole & pyrvinium), psychotic disorders (thioridazine, clomipramine & phenothiazines), alcoholism (disulfiram), lipid disorder (statins), inflammatory diseases (tranilast, auranofin, acetaminophen & celecoxib), antibiotics (azithromycin), and other disorders. Current research findings advocate the existence of beneficial effects by combining these repurposed drugs, and also through their complementary use with conventional cancer therapies.
Repurposing FDA-approved medications towards cancer care, by targeting the resistant CSCs, will allow for a quicker, cheaper development and approval process. A larger drug library available to physicians will allow for increased efficacy during both first-line and recurrent cancer treatments.
癌症是一个涉及体细胞基因组中遗传和表观遗传变化的多步骤过程。遗传突变以及环境因素导致癌症的起始、促进和进展。转移使癌细胞能够通过循环和淋巴系统扩散;继发性肿瘤通常导致致命后果。最近的实验证据表明,癌症干细胞(CSC)在肿瘤进展中起关键作用。肿瘤是异质的,由不同的细胞类型组成。CSC 是肿瘤细胞的一个亚群,具有自我更新和分化的能力。
本研究旨在介绍重新定位的药物和潜在的候选药物,这些药物可以作为抗癌药物,旨在针对耐药癌细胞,即 CSC。
对重新定位的药物或药物组合进行了研究出版物、FDA 备案和专利的审查,这些药物可以用于改善癌症治疗和护理。
针对 CSC 的药物包括用于治疗糖尿病(二甲双胍和噻唑烷二酮)、寄生虫病(氯喹、硝氯酚、甲苯达唑和吡喹酮)、精神障碍(硫利达嗪、氯米帕明和吩噻嗪)、酒精中毒(双硫仑)、脂质紊乱(他汀类药物)、炎症性疾病(曲尼司特、金诺芬、对乙酰氨基酚和塞来昔布)、抗生素(阿奇霉素)和其他疾病的药物。目前的研究结果表明,通过联合使用这些重新定位的药物,以及与常规癌症治疗互补使用,可以发挥有益的作用。
通过针对耐药 CSC 来重新定位 FDA 批准的药物,将使癌症治疗的开发和批准过程更快、更便宜。医生可利用的更大的药物库将在一线和复发性癌症治疗中提高疗效。