Department of Biochemistry, Faculty of Veterinary Medicine, Damanhour University, Damanhour, 22511, Egypt.
Department of Hormones, Medical Research Division, National Research Center, Dokki, Giza, 12622, Egypt.
Naunyn Schmiedebergs Arch Pharmacol. 2020 Sep;393(9):1581-1598. doi: 10.1007/s00210-020-01898-y. Epub 2020 May 26.
Cancer is a worldwide disease that causes millions of cases of mortality and morbidity. The major problem associated with the cancer is its resistance to conventional therapy and a high relapse rate. The use of chemotherapy to treat cancer began at the start of the twentieth century with attempts to control cancer. In time advance, many cancer chemotherapeutic agents have been developed for cancer treatment with different mechanisms of action including the alkylating agents, antimetabolites, antimicrotubule, topoisomerase inhibitors, and cytotoxic antibiotics, all of which have toxic effects toward normal cells in the body. Here, we reviewed chemotherapeutics' anticancer role potentiation and safety by thymoquinone (TQ) alone or in combination with the most common therapeutic drugs. Our search was done through PubMed, Science Direct, Springer Link, Taylor & Francis Online, Wiley Online Library, Nature publication group, SAGE Journals, and Web of Science databases. We recognized that TQ-chemotherapeutics combination increased chemo-modulation to the anticancer effect of different chemotherapeutics and protected the normal body cells from the toxic injuries that are induced by chemotherapeutics based on its antioxidant power. Moreover, the current study investigates the possible combinatory effect of TQ and chemotherapeutics to control cancer stem cells through molecular docking targeting of wingless/integrated (Wnt) and Hedgehog (Hh). We found that TQ modulates the Wnt and Hh pathways, by binding with tankyrase-2 and smoothened 7TM receptor, respectively, more efficiently than most chemotherapeutics drugs, while methotrexate showed high-binding affinity compared with TQ. Therefore, we encourage researchers to investigate the chemo-modulatory potential and protective effects of TQ in combination with chemotherapeutics for either cancer or cancer stem cell treatment.
癌症是一种全球性疾病,导致数百万人死亡和发病。与癌症相关的主要问题是其对传统疗法的抵抗力和高复发率。化疗用于治疗癌症始于 20 世纪初,旨在控制癌症。随着时间的推移,已经开发出许多用于癌症治疗的癌症化疗药物,其作用机制不同,包括烷化剂、抗代谢物、抗微管、拓扑异构酶抑制剂和细胞毒性抗生素,所有这些药物都会对体内正常细胞产生毒性作用。在这里,我们通过查阅 PubMed、Science Direct、Springer Link、Taylor & Francis Online、Wiley Online Library、Nature publication group、SAGE Journals 和 Web of Science 数据库,综述了单独使用或与最常见的治疗药物联合使用时,百里醌(TQ)对化疗药物的抗癌作用增强和安全性的影响。我们发现,TQ-化疗药物联合使用可以增强不同化疗药物的化疗调节作用,并通过其抗氧化能力保护正常体细胞免受化疗药物诱导的毒性损伤。此外,本研究通过针对无翅/整合(Wnt)和 Hedgehog(Hh)的分子对接,研究了 TQ 和化疗药物联合控制癌症干细胞的可能组合效应。我们发现,TQ 通过与 tankyrase-2 和 smoothened 7TM 受体分别结合,比大多数化疗药物更有效地调节 Wnt 和 Hh 通路,而甲氨蝶呤与 TQ 相比具有更高的结合亲和力。因此,我们鼓励研究人员研究 TQ 与化疗药物联合使用的化疗调节潜力和保护作用,用于癌症或癌症干细胞的治疗。