Substituted Thiazole Derivatives Provide Corrective Anti-tumour and Anti-oxidant Activities against Ehrlich Ascites Carcinoma

被引:3
作者
Keshta, A. T. [1 ]
Ashour, Hanaa Kh. [2 ]
机构
[1] Zagazig Univ, Fac Sci, Chem Dept, Biochem Div, Zagazig, Egypt
[2] Suez Canal Univ, Fac Sci, Chem Dept, Zagazig, Egypt
关键词
2 Thiazole derivatives; anticancer activity; antioxidant activity; apoptosis; p53; cytochrome c; Ehrlich ascites carcinoma (EAC); ANTIMICROBIAL ACTIVITY; LIPID-PEROXIDATION; APOPTOSIS; SYSTEM; CANCER; BLOOD;
D O I
10.1134/S1607672922600270
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:123 / 131
页数:9
相关论文
共 35 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]  
Alkadi Hourieh, 2020, Infectious Disorders - Drug Targets, V20, P16, DOI 10.2174/1871526518666180628124323
[3]   Carboxamide appended quinoline moieties as potential anti-proliferative agents, apoptotic inducers and Pim-1 kinase inhibitors [J].
Ammar, Yousry A. ;
Elhagali, Gamil A. M. ;
Abusaif, Moustafa S. ;
Selim, Mohamed R. ;
Zahran, Medhat A. ;
Naser, Tamer ;
Mehany, Ahmed B. M. ;
Fayed, Eman A. .
MEDICINAL CHEMISTRY RESEARCH, 2021, 30 (09) :1649-1668
[4]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[5]   Chemopreventive Property of Trichosanthes dioica Root Against 3-Methylcholanthrene-induced Carcinogenesis in Albino Mice [J].
Bhattacharya, Sanjib ;
Haldar, Pallab Kanti .
JOURNAL OF ENVIRONMENTAL PATHOLOGY TOXICOLOGY AND ONCOLOGY, 2012, 31 (02) :109-119
[6]   Mitochondrial control of apoptosis:: the role of cytochrome c [J].
Cai, JY ;
Yang, J ;
Jones, DP .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1366 (1-2) :139-149
[7]   Stiction - definition, modelling, detection and quantification [J].
Choudhury, M. A. A. Shoukat ;
Jain, Mridul ;
Shah, Sirish L. .
JOURNAL OF PROCESS CONTROL, 2008, 18 (3-4) :232-243
[8]   Evaluation of antitumor activity and in vivo antioxidant status of Anthocephalus cadamba on Ehrlich ascites carcinoma treated mice [J].
Dolai, Narayan ;
Karmakar, Indrajit ;
Kumar, R. B. Suresh ;
Kar, Biswakanth ;
Bala, Asis ;
Haldar, Pallab Kanti .
JOURNAL OF ETHNOPHARMACOLOGY, 2012, 142 (03) :865-870
[9]  
Halliwell B., 2015, Free radicals in biology and medicine
[10]   Relationship between DNA damage and total antioxidant capacity in patients with transitional meningioma [J].
Hanimoglu, Hakan ;
Tanriverdi, Taner ;
Kacira, Tibet ;
Sanus, Galip Zihni ;
Atukeren, Pinar ;
Aydin, Sabri ;
Tunali, Yusuf ;
Gumustas, Koray ;
Kaynar, Mehmet Yasar .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2007, 109 (07) :561-566