Biochemistry Division, Chemistry Department, Faculty of Science, Zagazig University, Zagazig, Egypt.
Chemistry Department, Faculty of Science, Suez Canal University, Zagazig, Egypt.
Dokl Biochem Biophys. 2023 Jun;510(1):123-131. doi: 10.1134/S1607672922600270. Epub 2023 Aug 15.
Novel and effective treatments are urgently needed for cancer, which is still the leading cause of death in the world. Biological characteristics linked to thiazole derivatives span a wide range. Thiazole derivatives are used in the creation of medications for therapy as well. The aim of current study is to evaluate the anticancer and antioxidant properties of the newly synthesized thiazole derivatives, compounds 1 and 2, on Ehrlich ascites carcinoma (EAC) cells in female mice. Our findings indicated that thiazole derivatives, compounds 1 and 2 have anticancer activity by elevating the p53 expression and cytochrome c levels in groups treated with compounds 1 and 2 compared to the positive control group. Furthermore, thiazole derivatives compounds 1 and 2 showed a potent antioxidant effect by increasing enzymatic antioxidants, catalase (CAT) activity, and non-enzymatic antioxidants, GSH, and lowering Malondialdehyde (MDA) in hepatic and renal tissues of treated groups. Additionally, the target compounds were capable of providing corrective effects against EAC-induced biochemical and histopathological changes without harmful side effects. CONCLUSION: The target studied thiazol derivatives compounds were capable of providing corrective effects against EAC-induced without harmful side effects.
新型有效的癌症治疗方法亟待开发,而癌症仍然是全球主要致死病因。噻唑衍生物的生物学特性广泛存在。噻唑衍生物也被用于治疗药物的研发。本研究旨在评估新型噻唑衍生物 1 和 2 对雌性小鼠艾氏腹水癌细胞(EAC)的抗癌和抗氧化特性。我们的研究结果表明,与阳性对照组相比,噻唑衍生物 1 和 2 可通过上调 p53 表达和细胞色素 c 水平,发挥抗癌活性。此外,噻唑衍生物 1 和 2 还具有较强的抗氧化作用,可通过增加肝肾功能组织中的酶抗氧化剂(CAT)活性、非酶抗氧化剂(GSH),降低丙二醛(MDA)水平。此外,目标化合物能够针对 EAC 引起的生化和组织病理学变化提供纠正作用,且无不良副作用。结论:研究中的目标噻唑衍生物化合物能够针对 EAC 引起的变化提供纠正作用,且无不良副作用。