Pregled bibliografske jedinice broj: 1215092
CYTOTOXIC EFFECT OF THIENO[2,3-B]PYRIDINE DERIVATIVES ON HUMAN BLADDER CANCER CELLS
CYTOTOXIC EFFECT OF THIENO[2,3-B]PYRIDINE DERIVATIVES ON HUMAN BLADDER CANCER CELLS, 2022., diplomski rad, diplomski, Medicinski fakultet, Split
CROSBI ID: 1215092 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
CYTOTOXIC EFFECT OF THIENO[2,3-B]PYRIDINE
DERIVATIVES ON HUMAN BLADDER CANCER CELLS
(Citotoksično djelovanje tieno[2,3-b]piridinskih
spojeva na stanice humanog karcinoma mokraćnog
mjehura)
Autori
Kalezić, Denis
Vrsta, podvrsta i kategorija rada
Ocjenski radovi, diplomski rad, diplomski
Fakultet
Medicinski fakultet
Mjesto
Split
Datum
15.09
Godina
2022
Stranica
49
Mentor
Čikeš Čulić, Vedrana
Ključne riječi
bladder cancer, thieno pyridine derivatives
(karcinom mokraćnog mjehura, tieno-piridinski derivati)
Sažetak
Objectives: The purpose of this study was to determine the effects of treating bladder cancer cells with the newly synthesized thieno[2, 3- b]pyridine anticancer agents, by focusing on its cytotoxic effects on the investigated human cell line T24. Methods: The T24 bladder cancer cell line was treated with a newly developed thieno[2, 3- b]pyridine anticancer compounds: Inhibitor 5 3- amino-N-(3-chloro-2-methylphenyl)-5-oxo-5, 6, 7, 8- tetrahydrothieno[2, 3-b]quinoline-2-carboxamide, Inhibitor 6 3-amino-N-(naphthalen-1-yl)-5-oxo- 5, 6, 7, 8-tetrahydrothieno[2, 3-b]quinoline-2- carboxamide, Inhibitor 8 (E)-3-amino-5-(3-(3- bromophenyl)acryloyl)-N-(3-chloro-2- methylphenyl)-6-methylthieno[2, 3-b]pyridine-2- carboxamide and Inhibitor 9 (E)-3-amino-5-(3-(3- bromophenyl)-1-hydroxyallyl)-N-(3-chloro-2- methylphenyl)-6-methylthieno[2, 3-b]pyridine-2- carboxamide to determine its cytotoxic effect on T24 cells. The 3-(4, 5-dimethylthiazolyl-2)-2, 5- diphenyltetrazolium bromide (MTT) assay was performed to analyze the cellular metabolic activity and determine the cytotoxic effect. Results: Inhibitors 5, 6, 8 and 9 all showed significant cytotoxic effect on the bladder cancer cells in a dose- and time-dependent manner. The most effective was Inhibitor 8 with an IC50 value of 0.4041 µg/mL after 72 hours. Conclusion: Due to their cytotoxic effect on bladder cancer cells, Inhibitors 5, 6, 8 and 9 deserve further attention as a potential treatment for transitional cell cancer.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti