Cytotoxic potential of dispirooxindolo/acenaphthoquino andrographolide derivatives against MCF-7 cell lineElectronic supplementary information (ESI) available. See DOI: 10.1039/c4md00469h

Dispiro andrographolide derivatives have been prepared from isatin/acenaphthoquinone, N -benzyl glycine and andrographolide via azomethine ylide cycloaddition reaction. The cytotoxic effect of the synthesized molecules has been studied against MCF-7 breast cancer cell line. The compounds induced apo...

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Hauptverfasser: Chakraborty, Debanjana, Maity, Arindam, Jain, Chetan K, Hazra, Abhijit, Bharitkar, Yogesh P, Jha, Tarun, Majumder, Hemanta K, Roychoudhury, Susanta, Mondal, Nirup B
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Sprache:eng
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Zusammenfassung:Dispiro andrographolide derivatives have been prepared from isatin/acenaphthoquinone, N -benzyl glycine and andrographolide via azomethine ylide cycloaddition reaction. The cytotoxic effect of the synthesized molecules has been studied against MCF-7 breast cancer cell line. The compounds induced apoptotic cell death as revealed by increased labeling with Annexin-V, decreased polarization of cell mitochondria, and increased reactive oxygen species production. Using FACS and western blot analysis, the compounds were observed to block the cell cycle at S phase. Activation of caspases 7 and 9 suggested that caspase pathways were involved in inducing apoptosis. Dispiro andrographolides induce a caspase-dependent apoptotic cell death pathway in breast cancer (MCF-7) cells.
ISSN:2040-2503
2040-2511
DOI:10.1039/c4md00469h