Pregled bibliografske jedinice broj: 819173
Organometallic iridium complexes as potential anticancer drugs
Organometallic iridium complexes as potential anticancer drugs // EMBO Abstract Book "Cellular signalling and cancer therapy"
Cavtat, Hrvatska, 2016. 1, 1 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 819173 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Organometallic iridium complexes as potential anticancer drugs
Autori
Gržan, Tena ; Kralj, Juran ; Bolje, Aljoša ; Tupek, Ana ; Steiner, Ivana ; Stojanović, Nikolina ; Hochloch, Stephan ; Polančec, Denis ; Osmak, Maja ; Sarkar, Biprajit ; Košmrlj, Janez ; Brozović, Anamaria
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
EMBO Abstract Book "Cellular signalling and cancer therapy"
/ - , 2016
Skup
Cellular signalling and cancer therapy - EMBO Conference
Mjesto i datum
Cavtat, Hrvatska, 27.05.2016. - 31.05.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
anticancer therapy ; organometallic ; complexes ; irridium
Sažetak
By using click chemistry approach several new metal complexes with chelating pyridyltriazolylidene ligands were synthesized. Their cytotoxic activity was determined on human cervical carcinoma HeLa cell line by spectrophotometric MTT assay. Compounds ABB43 and SH590 were mostly cytotoxic, with IC50 values of 7.33 μM and 2.01 μM, respectively. Both compounds are organoiridium complexes differing in N1 substituent at the click triazole moiety. Examination of their cytotoxic effect on different cell lines revealed that they preferential kill cancer cells over nontumorigenic cells. Further experiments were performed on HeLa cell line due to their high sensitivity to both investigated complexes. ABB43 and SH590 arrested HeLa cells in S/G2 phase of cell cycle and they induced apoptosis as explored through measurement of Annexin V and propidium iodide binding and measurement of their fluorescence by flow cytometer. To shed more light on the mechanisms responsible for the cytotoxic effect of ABB43 and SH590, we pre-treated HeLa cells with buthionine sulfoximine (inhibitor of glutathione synthesis) and found decreased cell survival upon treatment of cells with either of investigated complexes alone. The pre-treatment of cells with N-acetyl-cysteine (precursor in glutathione synthesis) resulted with opposite effect indicating the possible role of glutathione in protection of cells against ABB43 and SH590 cytotoxicity. We speculate that iridium complexes induce reactive oxidative species in treated cells, which further trigger cell death. Based on the gained knowledge, the development of more tumor-specific anticancer metal complexes as potential anticancer drugs is expected.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Anamaria Brozović
(autor)
Maja Osmak
(autor)
Denis Polančec
(autor)
Tena Gržan
(autor)
Juran Kralj
(autor)