Anticancer and antiangiogenesis activities of novel synthesized 2-substituted benzimidazoles molecules

Authors : Adem GÜNER, Elifsu POLATLI, Tamer AKKAN, Hakan BEKTAŞ, Canan ALBAY

Pages : 1270-1289

View : 18 | Download : 10

Publication Date : 0000-00-00

Article Type : Research Paper

Abstract :In this study, novel 2-substituted benzimidazoles molecules having triazole, thiadiazole, and oxadiazole rings were synthesized and were evaluated by anticancer, antioxidant/oxidant status, genotoxicity, and antiangiogenesis assays. Anticancer activity of the compounds was determined by MTT insert ignore into journalissuearticles values(0.5, 5, and 50 $\mu $g/mL); and lactate dehydrogenase insert ignore into journalissuearticles values(LDH); release assays against human prostate and breast cancer cells. Oxidative status of cells was elicited by total oxidative stress and total antioxidant capacity methods. Chick chorioallantoic membrane assay was used to evaluate the antiangiogenic activity. Genotoxicity was evaluated by the sister chromatid exchange insert ignore into journalissuearticles values(SCE); and micronucleus insert ignore into journalissuearticles values(MN); tests in lymphocyte cultured human blood. Our results showed that some of the compounds synthesized had significant antiproliferative activity against both cancer cell lines insert ignore into journalissuearticles values(between 4.54 $\pm $ 0.35 and 20.17 $\pm $ 3.15 $\mu $g/mL);, with higher inhibition of the breast cancer, and caused inhibition of LDH release with a linear correlation to MTT results. Moreover, the 5 $\mu $g/mL dose of these molecules led to an increase in antioxidant levels. Compounds had antiangiogenic effectiveness in a dose-dependent manner. Additionally, all of the compounds did not affect SCE and MN levels compared to controls. In conclusion, these newly synthesized molecules can be a resource of new anticancer agents with their nongenotoxic, antiproliferative, and antiangiogenic properties.
Keywords : Antiangiogenesis, anticancer, benzimidazole, cytotoxicity, genotoxicity