The Effects of Resveratrol-Rich Extracts of IVitis vinifera/I Pruning Waste on HeLa, MCF-7 and MRC-5 Cells: Apoptosis, Autophagia and Necrosis Interplay

Resveratrol is a well-studied plant-derived molecule in cancer biology, with a plethora of documented in vitro effects. However, its low bioavailability and toxicity risk hamper its wider use. In this study, vine shoots after pruning were used as a source of resveratrol (RSV). The activity of subcri...

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Veröffentlicht in:Pharmaceutics 2022-09, Vol.14 (10)
Hauptverfasser: Jovanović Galović, Aleksandra, Jovanović Lješković, Nataša, Vidović, Senka, Vladić, Jelena, Jojić, Nikola, Ilić, Milan, Srdić Rajić, Tatjana, Kojić, Vesna, Jakimov, Dimitar
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Sprache:eng
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Zusammenfassung:Resveratrol is a well-studied plant-derived molecule in cancer biology, with a plethora of documented in vitro effects. However, its low bioavailability and toxicity risk hamper its wider use. In this study, vine shoots after pruning were used as a source of resveratrol (RSV). The activity of subcritical water extract (SWE) and dry extract (DE) is examined on three cell lines: HeLa, MCF-7 and MRC-5. The cytotoxic effect is assessed by the MTT test and EB/AO staining, levels of apoptosis are determined by Annexin V assay, autophagia by ULK-1 expression using Western blot and NF-kB activation by p65 ELISA. Our results show that both resveratrol-rich extracts (DE, SWE) have a preferential cytotoxic effect on malignant cell lines (HeLa, MCF-7), and low cytotoxicity on non-malignant cells in culture (MRC-5). Further experiments indicate that the investigated malignant cells undergo different cell death pathways. MCF-7 cells died preferentially by apoptosis, while the HeLa cells died most likely by necrosis (possibly ferroptosis). Protective autophagia is diminished upon treatment with DE in both HeLa and MCF-7 cells, while SWE does not influence the level of autophagia. The extracts are effective even at low concentrations (below IC[sub.50] ) in the activation of NF-kB (p65 translocation).
ISSN:1999-4923
1999-4923
DOI:10.3390/pharmaceutics14102017