Design, synthesis and biological evaluation of new bis(thiosemicarbazone) derivatives as potential targeted anticancer agents for non-small cell lung cancer

Creative Commons License

Sever B., Akalın Çiftçi G., Özdemir A., Altıntop M. D.

JOURNAL OF RESEARCH IN PHARMACY, vol.24, no.5, pp.670-680, 2020 (ESCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 24 Issue: 5
  • Publication Date: 2020
  • Doi Number: 10.35333/jrp.2020.222
  • Journal Indexes: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.670-680
  • Keywords: Apoptosis, bis(thiosemicarbazone), cyclooxygenase-2, mitochondrial membrane potential, non-small cell lung cancer, THIOSEMICARBAZONE DERIVATIVES, IN-VITRO, COX-2, INHIBITORS, COMPLEXES, OLD
  • Anadolu University Affiliated: Yes


Thiosemicarbazones represent an important class of ligands for targeted therapy of many types of cancer including non-small cell lung cancer. In order to identify potential antitumor agents for targeted therapy of lung cancer, new bis(thiosemicarbazone) derivatives (1-11) were prepared via the reaction of 1,4-phenylenebis(thiosemicarbazide) with 5-arylfurfurals. The cytotoxic effects of compounds 1-11 on A549 human lung adenocarcinoma and L929 mouse fibroblast cells were investigated using MTT test. Compounds 1, 10 and 11 were the most potent anticancer agents in this series on A549 cell line with IC50 values of 14.33 ± 0.47 µg/mL, 11.67 ± 2.49 µg/mL and 16.67 ± 5.56 µg/mL, respectively compared to cisplatin (IC50 = 18.33 ± 0.94 mu g/mL). Based on their IC50 values for L929 cell line, their anticancer activities were found to be selective. Moreover, flow cytometry-based analyses were performed to examine their effects on apoptosis and mitochondrial membrane potential. The treatment of A549 cells with compounds 1, 10 and 11 at IC50 concentrations led to the induction of apoptosis along with mitochondrial membrane depolarization. In order to explore their mode of action, compounds 1, 10 and 11 were evaluated for their inhibitory effects on COX-1 and COX-2 in A549 cells. In particular, N,N'-(1,4-phenylene)bis(2-((5-(2,5-dichlorophenyl)furan-2-yl)methylene)hydrazine-1-carbothioamide) (10) was identified as a selective COX-2 inhibitor (6.96% for COX-1 and 54.81% for COX-2). According to these results, compound 10 warrants further in vitro and in vivo studies as a potential targeted anticancer agent for the management of non-small cell lung cancer.