Publication Details |
| Category | Text Publication |
| Reference Category | Journals |
| DOI | 10.2298/JSC240109018H |
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| Title (Primary) | In vitro anticancer studies of a small library of cyclic lipopeptides against the human cervix adenocarcinoma HeLa cells |
| Author | Hmedat, A.N.; Chávez Morejón, M.; Rivera, D.G.; Pantelic, N.Đ.; Wessjohann, L.A.; Kaluđerović, G.N. |
| Source Titel | Journal of the Serbian Chemical Society |
| Year | 2024 |
| Department | MIBITECH |
| Volume | 89 |
| Issue | 4 |
| Page From | 471 |
| Page To | 484 |
| Language | englisch |
| Topic | T7 Bioeconomy |
| Supplements | https://www.shd-pub.org.rs/index.php/JSCS/article/view/12766/10532 |
| Keywords | cancer; surfactin; proliferation; apoptosis; cell cycle; autophagy |
| Abstract | Various cyclic lipopeptides (CLPs, 23 compounds) were tested for their antitumor potential against human cervix adenocarcinoma HeLa cells. From the fast screening (tested concentrations: 0.01 and 10 μM) compound 10 ((12S,6S,10S,13S)-6-((R)-sec-butyl)-7-(2-(dodecylamino)-2-oxoethyl)-13-isopropyl- 82-nitro-2,5,12,15-tetraoxo-4,7,11,14-tetraaza-1(1,2)-pyrrolidina-8(1,4)-benzenacyclopentadecaphane- 10-carboxamide) was identified as active against HeLa cell line. The MTT 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and CV (crystal violet) assays revealed at least five times higher cytotoxic potential of 10 (IC50 = 12.3±1.8 μM, MTT; 9.4±1.5 μM; CV) in comparison to control drug natural occurring CLP surfactin (IC50 = 64.9±0.8 μM, MTT; 76.2±1.6 μM; CV). The cell cycle analysis performed by DAPI (4',6-diamidino- 2-phenylindole) assay indicated the involvement of apoptosis in HeLa cell death upon treatment with 10, which was confirmed by apoptosis assay (annexin V/PI). Furthermore, during this process caspase activation could be detected (ApoStat assay, immunocytochemistry caspase-3 analysis). The flow cytometry analysis did not display induction of autophagy as a possible death mechanism in HeLa cells upon 10 treatment. The current findings could be used to design more effective CLPs based on 10 structure as potential anticancer agents. |
| Persistent UFZ Identifier | https://www.ufz.de/index.php?en=20939&ufzPublicationIdentifier=29304 |
| Hmedat, A.N., Chávez Morejón, M., Rivera, D.G., Pantelic, N.Đ., Wessjohann, L.A., Kaluđerović, G.N. (2024): In vitro anticancer studies of a small library of cyclic lipopeptides against the human cervix adenocarcinoma HeLa cells J. Serb. Chem. Soc. 89 (4), 471 - 484 10.2298/JSC240109018H |
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