In vitro antiproliferative and cytotoxic activities of novel triphenyltin isoselenocyanate in human breast carcinoma cell lines MCF 7 and MDA-MB-231

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Publikace nespadá pod Filozofickou fakultu, ale pod Farmaceutickou fakultu. Oficiální stránka publikace je na webu muni.cz.
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HUNAKOVA L. HORVATHOVA E. MATUSKOVA M. BOBÁĽ Pavel OTEVŘEL Jan BRTKO J.

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj Medical Oncology
Fakulta / Pracoviště MU

Farmaceutická fakulta

Citace
www https://link.springer.com/content/pdf/10.1007/s12032-022-01692-1.pdf
Doi http://dx.doi.org/10.1007/s12032-022-01692-1
Klíčová slova Apoptosis; Breast cancer; Cytotoxicity; DNA crosslinks; Migration; Triorganotin isoselenocyanates
Popis Intensive investigation for novel antiproliferative and cytotoxic effective chemical compounds is currently concentrated on structurally modified agents of natural or synthetic source. The selenium derivative of triorganotin compound, triphenyltin isoselenocyanate (TPT-NCSe) caused higher cytotoxicity in hormone sensitive MCF 7 (IC 50-250 nM) in comparison with triple-negative MDA-MB-231 breast carcinoma cell line (IC 50-450 nM) as determined by MTT assay. Measurement of DNA damage showed presence of crosslinks in both cell lines treated by increasing TPT-NCSe concentrations. This compound decreased mitochondrial membrane potential shown by JC-1 staining in a concentration-dependent manner in both cell lines. Activation of caspases-3/7 was observed in MDA-MB-231 cells and was significant only by concentrations causing significant level of crosslinks. On the other hand, migration assay revealed inhibitory effect of viability keeping 100 nM concentration of TPT-NCSe on migration of MDA-MB-231 cells. Our data has shown that this selenium containing triorganotin molecule exerts DNA damage-linked antineoplastic activity in breast carcinoma cell lines studied.
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