Abstract
TARGETED THERAPY IN SQUAMOUS CELL CARCINOMA: INVESTIGATING THE ROLE OF SYNTHETIC ANALOG MOLECULES
Syed Majid*, Sumaiyya Mehreen and Ayesha Munawar
ABSTRACT
Aim: To evaluate the cytotoxic effects of Benzaldehyde 3-chloro-4-fluorophenylhydrazone, a PD-1 immune checkpoint inhibitor, on kidney cancer cell lines and compare its efficacy with Cisplatin using various in vitro assays. Objective: To assess Benzaldehyde 3-chloro-4-fluorophenylhydrazone's potential as a therapeutic alternative or adjunct to Cisplatin for the treatment of Squamous Cell Carcinoma (SCC). Research: Kidney cancer cell lines were treated with different concentrations of Benzaldehyde 3-chloro-4-fluorophenylhydrazone and Cisplatin. Five cell viability assays were performed, namely MTT, CellTiter-Glo, Alamar Blue, Sulforhodamine B (SRB), and LDH cytotoxicity assays. The results showed a dose-dependent decrease in cell viability with Benzaldehyde 3-chloro-4-fluorophenylhydrazone, similar to the effects observed with Cisplatin. The LDH cytotoxicity assay indicated substantial cell membrane damage at higher Benzaldehyde 3-chloro-4-fluorophenylhydrazone concentrations, suggesting its potential as a cytotoxic agent. Conclusion: Benzaldehyde 3-chloro-4-fluorophenylhydrazone demonstrated strong cytotoxic effects across multiple assay methods and showed comparable efficacy to Cisplatin at higher concentrations. These findings suggest that Benzaldehyde 3-chloro-4-fluorophenylhydrazone could serve as a viable alternative or complement to traditional chemotherapy for SCC treatment, warranting further clinical investigations.
[Full Text Article] [Download Certificate]WJPLS CITATION
All | Since 2020 | |
Citation | 590 | 424 |
h-index | 12 | 10 |
i10-index | 17 | 14 |
INDEXING
NEWS & UPDATION
BEST ARTICLE AWARDS
World Journal of Pharmaceutical and life sciences is giving Best Article Award in every Issue for Best Article and Issue Certificate of Appreciation to the Authors to promote research activity of scholar.
Best Article of current issue
Download Article : Click here