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The Cytotoxic Effect of Apis mellifera Venom with a Synergistic Potential of Its Two Main Components—Melittin and PLA2—On Colon Cancer HCT116 Cell Lines

Authors :
Ziad Fajloun
Bruno Coutard
Dany El-Obeid
Jean-Marc Sabatier
Mariam Rifi
Carole Yaacoub
Hiba Mawlawi
Institut de neurophysiopathologie (INP)
Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
Source :
Molecules, Volume 26, Issue 8, Molecules, MDPI, 2021, 26 (8), pp.2264. ⟨10.3390/molecules26082264⟩, Molecules, Vol 26, Iss 2264, p 2264 (2021), Molecules, 2021, 26 (8), pp.2264. ⟨10.3390/molecules26082264⟩
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Colon carcinogenesis is ranked second globally among human diseases after cardiovascular failures. Bee venom (BV) has been shown to possess in vitro anticancer effects against several types of cancer cells. The two main biopeptides of Apis mellifera BV, namely, melittin (MEL) and phospholipase A2 (PLA2), are suspected to be the biomolecules responsible for the anticancer activity. The present work aims to evaluate the cytotoxic effect of the A. mellifera venom on human colon carcinoma cells (HCT116), and to assess the synergistic effect of MEL and PLA2 on these cells. After analyzing, through high-pressure liquid chromatography, the proportions of MEL and PLA2 on BV, we have established a cell viability assay to evaluate the effect of BV, MEL, PLA2, and a mixture of MEL and PLA2 on the HCT116 cells. Results obtained showed a strong cytotoxicity effect induced by the A. mellifera venom and to a lower extent MEL or PLA2 alone. Remarkably, when MEL and PLA2 were added together, their cytotoxic effect was greatly improved, suggesting a synergistic activity on HCT116 cells. These findings confirm the cytotoxic effect of the A. mellifera venom and highlight the presence of synergistic potential activities between MEL and PLA2, possibly inducing membrane disruption of HCT116 cancer cells. Altogether, these results could serve as a basis for the development of new anticancer treatments.

Details

ISSN :
14203049
Volume :
26
Database :
OpenAIRE
Journal :
Molecules
Accession number :
edsair.doi.dedup.....950177cde97e1d10ed963e499e3a5d15
Full Text :
https://doi.org/10.3390/molecules26082264