Concomitant reduction of c-Myc expression and PI3K/AKT/mTOR signaling by quercetin induces a strong cytotoxic effect against Burkitt's lymphoma. (October 2016)
- Record Type:
- Journal Article
- Title:
- Concomitant reduction of c-Myc expression and PI3K/AKT/mTOR signaling by quercetin induces a strong cytotoxic effect against Burkitt's lymphoma. (October 2016)
- Main Title:
- Concomitant reduction of c-Myc expression and PI3K/AKT/mTOR signaling by quercetin induces a strong cytotoxic effect against Burkitt's lymphoma
- Authors:
- Granato, Marisa
Rizzello, Celeste
Romeo, Maria Anele
Yadav, Shivangi
Santarelli, Roberta
D'Orazi, Gabriella
Faggioni, Alberto
Cirone, Mara - Abstract:
- Abstract: Burkitt's lymphoma is an aggressive B cell lymphoma whose pathogenesis involves mainly c-Myc translocation and hyperexpression, in addition to antigen-independent BCR signaling and, in some cases, EBV infection. As result of BCR signaling activation, the PI3K/AKT/mTOR pathway results constitutively activated also in the absence of EBV, promoting cell survival and counterbalancing the pro-apoptotic function that c-Myc may also exert. In this study we found that quercetin, a bioflavonoid widely distributed in plant kingdom, reduced c-Myc expression and inhibited the PI3K/AKT/mTOR activity in BL, leading to an apoptotic cell death. We observed a higher cytotoxic effect against the EBV-negative BL cells in comparison with the positive ones, suggesting that this oncogenic gammaherpesvirus confers an additional resistance to the quercetin treatment. Besides cell survival, PI3K/AKT/mTOR pathway also regulates autophagy: we found that quercetin induced a complete autophagic flux in BL cells, that contributes to c-Myc reduction in some of these cells. Indeed, autophagy inhibition by chloroquine partially restored c-Myc expression in EBV-positive (Akata) and EBV-negative (2A8) cells that harbor c-Myc mutation. Interestingly, chloroquine did not affect the quercetin-mediated reduction of c-Myc expression in Ramos cells, that have no c-Myc mutation in the coding region, although autophagy was induced. These results suggest that mutant c-Myc could be partially degraded throughAbstract: Burkitt's lymphoma is an aggressive B cell lymphoma whose pathogenesis involves mainly c-Myc translocation and hyperexpression, in addition to antigen-independent BCR signaling and, in some cases, EBV infection. As result of BCR signaling activation, the PI3K/AKT/mTOR pathway results constitutively activated also in the absence of EBV, promoting cell survival and counterbalancing the pro-apoptotic function that c-Myc may also exert. In this study we found that quercetin, a bioflavonoid widely distributed in plant kingdom, reduced c-Myc expression and inhibited the PI3K/AKT/mTOR activity in BL, leading to an apoptotic cell death. We observed a higher cytotoxic effect against the EBV-negative BL cells in comparison with the positive ones, suggesting that this oncogenic gammaherpesvirus confers an additional resistance to the quercetin treatment. Besides cell survival, PI3K/AKT/mTOR pathway also regulates autophagy: we found that quercetin induced a complete autophagic flux in BL cells, that contributes to c-Myc reduction in some of these cells. Indeed, autophagy inhibition by chloroquine partially restored c-Myc expression in EBV-positive (Akata) and EBV-negative (2A8) cells that harbor c-Myc mutation. Interestingly, chloroquine did not affect the quercetin-mediated reduction of c-Myc expression in Ramos cells, that have no c-Myc mutation in the coding region, although autophagy was induced. These results suggest that mutant c-Myc could be partially degraded through autophagy in BL cells, as previously reported for other mutant oncogenic proteins. … (more)
- Is Part Of:
- International journal of biochemistry & cell biology. Volume 79(2016:Oct.)
- Journal:
- International journal of biochemistry & cell biology
- Issue:
- Volume 79(2016:Oct.)
- Issue Display:
- Volume 79 (2016)
- Year:
- 2016
- Volume:
- 79
- Issue Sort Value:
- 2016-0079-0000-0000
- Page Start:
- 393
- Page End:
- 400
- Publication Date:
- 2016-10
- Subjects:
- Q quercetin -- BL Burkitt's lymphoma -- BCR B cell receptor -- GC Germinal Center -- EBV Epstein–Barr virus -- PI3K phosphatidylinositol-3-kinase -- AKT AKT or protein kinase B -- mTOR mammalian target of rapamycin -- BEZ235 NVP-BEZ235 -- I-c-Myc c-Myc inhibitor -- HSPs heat shock proteins -- PES 2-phenylethynesulfonamide -- CQ chloroquine -- PARP poly (ADP-ribose) polymerase -- LC3 microtubule-associated protein 1A/1B-light chain 3 -- 4E-BP1 eIF4E-binding protein -- c-Myc cellular myelocytomatosis oncogene -- NF-κB nuclear factor K-light-chain-enhancer of activated B cells -- Bcl-2 B-cell lymphoma 2 -- TCF-3 transcription factor 3 -- GSK3 glycogen synthase kinase 3 -- PES 2-phenylethyne-1-sulfonamide, 2-phenylethynesulfonamide
BL -- EBV -- Quercetin -- c-Myc -- PI3K/AKT/mTOR -- Autophagy
Biochemistry -- Periodicals
Cytology -- Periodicals
Biochemistry -- Periodicals
Cell Biology -- Periodicals
Biochimie -- Périodiques
Cytologie -- Périodiques
Biochimie
Cytologie
Biochemistry
Cytology
Ressource Internet (Descripteur de forme)
Périodique électronique (Descripteur de forme)
Periodicals
572.05 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13572725 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biocel.2016.09.006 ↗
- Languages:
- English
- ISSNs:
- 1357-2725
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.135000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2535.xml