GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma

Abstract Background Neuroblastoma (NB) is a frequent pediatric tumor associated with poor prognosis. The disregulation of Bcl-2, an anti-apoptotic protein, is crucial for the tumoral development and chemoresistance. Autophagy is also implicated in tumor cell survival and chemoresistance. The aim of...

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Main Authors: Sonia Cournoyer, Anissa Addioui, Assila Belounis, Mona Beaunoyer, Carine Nyalendo, Roxane Le Gall, Pierre Teira, Elie Haddad, Gilles Vassal, Hervé Sartelet
Format: Article
Language:English
Published: BMC 2019-10-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-019-6195-y
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spelling doaj-384d2fe4c3b04a5e9f90f3e292ea8d672020-11-25T04:03:21ZengBMCBMC Cancer1471-24072019-10-0119111410.1186/s12885-019-6195-yGX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastomaSonia Cournoyer0Anissa Addioui1Assila Belounis2Mona Beaunoyer3Carine Nyalendo4Roxane Le Gall5Pierre Teira6Elie Haddad7Gilles Vassal8Hervé Sartelet9Research Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterResearch Center, Sainte Justine University Hospital CenterDepartment of Pediatric Oncology, Institut Gustave RoussyResearch Center, Sainte Justine University Hospital CenterAbstract Background Neuroblastoma (NB) is a frequent pediatric tumor associated with poor prognosis. The disregulation of Bcl-2, an anti-apoptotic protein, is crucial for the tumoral development and chemoresistance. Autophagy is also implicated in tumor cell survival and chemoresistance. The aim of our study was to demonstrate therapeutic efficiency of GX 15–070, a pan-Bcl-2 family inhibitor, used alone and in combination with conventional drugs or with hydroxychloroquine (HCQ), an autophagy inhibitor. Methods Five neuroblastoma cell lines were tested for the cytotoxic activity of GX 15–070 alone or in combination with cisplatin, doxorubicin, HCQ or Z-VAD-FMK a broad-spectrum caspase inhibitor. Apoptosis and autophagy levels were studied by western-blot and FACS. Orthotopic injections were performed on NOD/LtSz-scid/IL-2Rgamma null mice that were treated with either GX 15–070 alone or in combination with HCQ. Results Synergistic cytotoxicity was observed for the drug combination in all of the 5 neuroblastoma cell lines tested, including MYCN amplified lines and in cancer stem cells. GX 15–070 significantly increased apoptosis and autophagy in neuroblastoma cells as evidenced by increased levels of the autophagy marker, LC3-II. Inhibition of autophagy by HCQ, further increased the cytotoxicity of this combinatorial treatment, suggesting that autophagy induced by these agent plays a cytoprotective role. In vivo, GX 15–070 combined with HCQ significantly decreased the growth of the tumor and the number of distant metastases. Conclusions Based on the synergistic effect of HCQ and GX 15–070 observed in this study, the combination of these two drugs may be utilized as a new therapeutic approach for neuroblastoma.http://link.springer.com/article/10.1186/s12885-019-6195-yBcl-2NeuroblastomaApoptosisAutophagyGX15–070
collection DOAJ
language English
format Article
sources DOAJ
author Sonia Cournoyer
Anissa Addioui
Assila Belounis
Mona Beaunoyer
Carine Nyalendo
Roxane Le Gall
Pierre Teira
Elie Haddad
Gilles Vassal
Hervé Sartelet
spellingShingle Sonia Cournoyer
Anissa Addioui
Assila Belounis
Mona Beaunoyer
Carine Nyalendo
Roxane Le Gall
Pierre Teira
Elie Haddad
Gilles Vassal
Hervé Sartelet
GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
BMC Cancer
Bcl-2
Neuroblastoma
Apoptosis
Autophagy
GX15–070
author_facet Sonia Cournoyer
Anissa Addioui
Assila Belounis
Mona Beaunoyer
Carine Nyalendo
Roxane Le Gall
Pierre Teira
Elie Haddad
Gilles Vassal
Hervé Sartelet
author_sort Sonia Cournoyer
title GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
title_short GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
title_full GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
title_fullStr GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
title_full_unstemmed GX15–070 (Obatoclax), a Bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases Chemosensitivity in neuroblastoma
title_sort gx15–070 (obatoclax), a bcl-2 family proteins inhibitor engenders apoptosis and pro-survival autophagy and increases chemosensitivity in neuroblastoma
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2019-10-01
description Abstract Background Neuroblastoma (NB) is a frequent pediatric tumor associated with poor prognosis. The disregulation of Bcl-2, an anti-apoptotic protein, is crucial for the tumoral development and chemoresistance. Autophagy is also implicated in tumor cell survival and chemoresistance. The aim of our study was to demonstrate therapeutic efficiency of GX 15–070, a pan-Bcl-2 family inhibitor, used alone and in combination with conventional drugs or with hydroxychloroquine (HCQ), an autophagy inhibitor. Methods Five neuroblastoma cell lines were tested for the cytotoxic activity of GX 15–070 alone or in combination with cisplatin, doxorubicin, HCQ or Z-VAD-FMK a broad-spectrum caspase inhibitor. Apoptosis and autophagy levels were studied by western-blot and FACS. Orthotopic injections were performed on NOD/LtSz-scid/IL-2Rgamma null mice that were treated with either GX 15–070 alone or in combination with HCQ. Results Synergistic cytotoxicity was observed for the drug combination in all of the 5 neuroblastoma cell lines tested, including MYCN amplified lines and in cancer stem cells. GX 15–070 significantly increased apoptosis and autophagy in neuroblastoma cells as evidenced by increased levels of the autophagy marker, LC3-II. Inhibition of autophagy by HCQ, further increased the cytotoxicity of this combinatorial treatment, suggesting that autophagy induced by these agent plays a cytoprotective role. In vivo, GX 15–070 combined with HCQ significantly decreased the growth of the tumor and the number of distant metastases. Conclusions Based on the synergistic effect of HCQ and GX 15–070 observed in this study, the combination of these two drugs may be utilized as a new therapeutic approach for neuroblastoma.
topic Bcl-2
Neuroblastoma
Apoptosis
Autophagy
GX15–070
url http://link.springer.com/article/10.1186/s12885-019-6195-y
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