Article ; Online: Induction of G₂/M arrest, caspase activation and apoptosis by α-santonin derivatives in HL-60 cells.
Toxicology in vitro : an international journal published in association with BIBRA
2013 Volume 27, Issue 5, Page(s) 1458–1466
Abstract: ... a significant inhibition on cell-cycle progression and leading to an increasing of cells in G2/M [7.6% and 9.0 ... all compounds caused G2/M reduction and a significant DNA fragmentation. Compounds 2, 3 and 4 were able ...
Abstract | Sesquiterpene lactones (SLs) are natural products with a variety of biological activities. Previously, we demonstrated the cytotoxic effects of three new α-santonin derivatives on different tumor cell lines with low toxic effects upon peripheral human leukocytes. Here, we evaluated the mechanism of action triggered by these derivatives. HL-60 cell cycle determined after 24h treatment revealed a significant inhibition on cell-cycle progression and leading to an increasing of cells in G2/M [7.6% and 9.0% for compound 3% and 9.0% and 8.6% for compound 4 (1 and 2 μM, respectively)]. However, after 48 h exposure, all compounds caused G2/M reduction and a significant DNA fragmentation. Compounds 2, 3 and 4 were able to induce apoptosis on leukemia cells, which was corroborated by phosphatidyserine externalization and activation of caspases-3 and -7 after 24h exposure. None of the derivatives analyzed caused depolarization of mitochondrial membrane within 24h of incubation, suggesting the involvement of the extrinsic apoptotic pathway in the death process. The antiproliferative action of these compounds is related to the DNA synthesis inhibition and cell cycle arrest, which probably lead to apoptosis activation. Therefore, these santonin derivatives are promising lead candidates for development of new cytotoxic agents. |
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MeSH term(s) | Apoptosis/drug effects ; Caspase 3/metabolism ; Caspase 7/metabolism ; Cell Cycle Checkpoints/drug effects ; Cell Proliferation/drug effects ; Cytotoxins/pharmacology ; DNA Fragmentation ; G2 Phase ; HL-60 Cells ; Humans ; Membrane Potential, Mitochondrial/drug effects ; Santonin/analogs & derivatives ; Santonin/pharmacology |
Chemical Substances | Cytotoxins ; Santonin (1VL8J38ERO) ; Caspase 3 (EC 3.4.22.-) ; Caspase 7 (EC 3.4.22.-) |
Language | English |
Publishing date | 2013-08 |
Publishing country | England |
Document type | Journal Article ; Research Support, Non-U.S. Gov't |
ZDB-ID | 639064-x |
ISSN | 1879-3177 ; 0887-2333 |
ISSN (online) | 1879-3177 |
ISSN | 0887-2333 |
DOI | 10.1016/j.tiv.2013.03.010 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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