RETRACTED: Moringa isothiocyanate complexed with α-cyclodextrin: a new perspective in neuroblastoma treatment (Retracted article. See vol. 23, 2023)

被引:21
|
作者
Giacoppo, Sabrina [1 ]
Iori, Renato [2 ]
Rollin, Patrick [3 ,4 ]
Bramanti, Placido [1 ]
Mazzon, Emanuela [1 ]
机构
[1] IRCCS Ctr Neurolesi Bonino Pulejo, Via Provinciale Palermo, I-98124 Messina, Italy
[2] Ctr Ric Agr & Ambiente CREA AA, Consiglio Ric Agr & Anal Econ Agr, Via Corticella 133, I-40128 Bologna, Italy
[3] Univ Orleans, BP 6759, F-45067 Orleans, France
[4] CNRS, ICOA, UMR 7311, BP 6759, F-45067 Orleans, France
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2017年 / 17卷
关键词
SH-SY5Y human neuroblastoma cells; Moringa isothiocyanate; alpha-CD-complexed moringin; Anti-cancer drug; SIGNALING PATHWAY; CELL-DEATH; GLUCOMORINGIN ISOTHIOCYANATE; PI3K/AKT/MTOR PATHWAY; CANCER CELLS; SULFORAPHANE; APOPTOSIS; INFLAMMATION; CHILDREN; PROTEIN;
D O I
10.1186/s12906-017-1876-z
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Several lines of evidence suggest the consume of natural products for cancer prevention or treatment. In particular, isothiocyanates (ITCs) exerting anti-cancer properties, have received great interest as potential chemotherapeutic agents. This study was designed to assess the anti-proliferative activities of a new preparation of Moringa oleifera-derived 4-(alpha-L-rhamnopyranosyloxy) benzyl ITC (moringin) complexed with alpha-cyclodextrin (moringin + alpha-CD; MAC) on SH-SY5Y human neuroblastoma cells. This new formulation arises in the attempt to overcome the poor solubility and stability of moringin alone in aqueous media. Methods: SH-SY5Y cells were cultured and exposed to increasing concentrations of MAC (1.0, 2.5 and 5.0 mu g). Cell proliferation was examined by MTT and cell count assays. The cytotoxic activity of the MAC complex was assessed by lactate dehydrogenase (LDH) assay and trypan blue exclusion test. In addition, western blotting analyses for the main apoptosis-related proteins were performed. Results: Treatment of SH-SY5Y cells with the MAC complex reduced cell growth in concentration dependent manner. Specifically, MAC exhibited a potent action in inhibiting the PI3K/Akt/mTOR pathway, whose aberrant activation was found in many types of cancer. MAC was also found to induce the nuclear factor-kappa B (NF-kappa B) p65 activation by phosphorylation and its translocation into the nucleus. Moreover, treatment with MAC was able to down-regulate MAPK pathway (results focused on JNK and p38 expression). Finally, MAC was found to trigger apoptotic death pathway (based on expression levels of cleaved-caspase 3, Bax/Bcl-2 balance, p53 and p21). Conclusion: These findings suggest that use of MAC complex may open novel perspectives to improve the poor prognosis of patients with neuroblastoma.
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页数:10
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