Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors
The resistance to chemotherapy and the tumor escape from host immunosurveillance are the main causes of the failure of anthracycline-based regimens in breast cancer, where an effective chemo-immunosensitizing strategy is lacking. The clinically used aminobisphosphonate zoledronic acid (ZA) reverses...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2016
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/17810
- Acceso en línea:
- http://repository.urosario.edu.co/handle/10336/17810
- Palabra clave:
- Hipoxia De La Célula
Neoplasias Del Cuello Uterino
Células Endoteliales
Microambiente Tumoral
Células Hela
Factores De Transcripción Stat
Estrés Fisiológico
Enfermedades
Neoplasias de la Mama
Epirrubicina
Pontos Quânticos
Células Tumorales Cultivadas
Self-Assembling Nanoparticles
Zoledronic Acid
Doxorubicin Resistance
Immunoresistance
Immunosuppression
- Rights
- License
- Abierto (Texto Completo)
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Repositorio EdocUR - U. Rosario |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
title |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
spellingShingle |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors Hipoxia De La Célula Neoplasias Del Cuello Uterino Células Endoteliales Microambiente Tumoral Células Hela Factores De Transcripción Stat Estrés Fisiológico Enfermedades Neoplasias de la Mama Epirrubicina Pontos Quânticos Células Tumorales Cultivadas Self-Assembling Nanoparticles Zoledronic Acid Doxorubicin Resistance Immunoresistance Immunosuppression |
title_short |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
title_full |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
title_fullStr |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
title_full_unstemmed |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
title_sort |
Zoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumors |
dc.contributor.gruplac.spa.fl_str_mv |
Bio-Bio |
dc.subject.spa.fl_str_mv |
Hipoxia De La Célula Neoplasias Del Cuello Uterino Células Endoteliales Microambiente Tumoral Células Hela Factores De Transcripción Stat Estrés Fisiológico |
topic |
Hipoxia De La Célula Neoplasias Del Cuello Uterino Células Endoteliales Microambiente Tumoral Células Hela Factores De Transcripción Stat Estrés Fisiológico Enfermedades Neoplasias de la Mama Epirrubicina Pontos Quânticos Células Tumorales Cultivadas Self-Assembling Nanoparticles Zoledronic Acid Doxorubicin Resistance Immunoresistance Immunosuppression |
dc.subject.ddc.none.fl_str_mv |
Enfermedades |
dc.subject.decs.spa.fl_str_mv |
Neoplasias de la Mama Epirrubicina Pontos Quânticos Células Tumorales Cultivadas |
dc.subject.keyword.eng.fl_str_mv |
Self-Assembling Nanoparticles Zoledronic Acid Doxorubicin Resistance Immunoresistance Immunosuppression |
description |
The resistance to chemotherapy and the tumor escape from host immunosurveillance are the main causes of the failure of anthracycline-based regimens in breast cancer, where an effective chemo-immunosensitizing strategy is lacking. The clinically used aminobisphosphonate zoledronic acid (ZA) reverses chemoresistance and immunoresistance in vitro. Previously we developed a nanoparticle-based zoledronic acid-containing formulation (NZ) that allowed a higher intratumor delivery of the drug compared with free ZA in vivo. We tested its efficacy in combination with doxorubicin in breast tumors refractory to chemotherapy and immune system recognition as a new combinatorial approach to produce chemo- and immunosensitization. NZ reduced the IC50 of doxorubicin in human and murine chemoresistant breast cancer cells and restored the doxorubicin efficacy against chemo-immunoresistant tumors implanted in immunocompetent mice. By reducing the metabolic flux through the mevalonate pathway, NZ lowered the activity of Ras/ERK1/2/HIF-1? axis and the expression of P-glycoprotein, decreased the glycolysis and the mitochondrial respiratory chain, induced a cytochrome c/caspase 9/caspase 3-dependent apoptosis, thus restoring the direct cytotoxic effects of doxorubicin on tumor cell. Moreover, NZ restored the doxorubicin-induced immunogenic cell death and reversed the tumorinduced immunosuppression due to the production of kynurenine, by inhibiting the STAT3/indoleamine 2,3 dioxygenase axis. These events increased the number of dendritic cells and decreased the number of immunosuppressive T-regulatory cells infiltrating the tumors. Our work proposes the use of nanoparticle encapsulating zoledronic acid as an effective tool overcoming at the same time chemoresistance and immunoresistance in breast tumors, thanks to the effects exerted on tumor cell and tumor-infiltrating immune cells. |
publishDate |
2016 |
dc.date.created.none.fl_str_mv |
2016 |
dc.date.issued.none.fl_str_mv |
2016 |
dc.date.accessioned.none.fl_str_mv |
2018-04-10T13:56:17Z |
dc.date.available.none.fl_str_mv |
2018-04-10T13:56:17Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.issn.none.fl_str_mv |
ISSN: 1949-2553 |
dc.identifier.uri.none.fl_str_mv |
http://repository.urosario.edu.co/handle/10336/17810 |
identifier_str_mv |
ISSN: 1949-2553 |
url |
http://repository.urosario.edu.co/handle/10336/17810 |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
20772 |
dc.relation.citationIssue.none.fl_str_mv |
No. 12 |
dc.relation.citationStartPage.none.fl_str_mv |
20753 |
dc.relation.citationTitle.none.fl_str_mv |
Oncotarget |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 15 |
dc.relation.ispartof.spa.fl_str_mv |
Oncotarget, ISSN: 1949-2553, Vol. 15/No.12 (April 2016) pp. 20753-20772 |
dc.relation.uri.none.fl_str_mv |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991490/ |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
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repository.mail.fl_str_mv |
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1814167621698846720 |
spelling |
Bio-BioKopecka, JoannaPorto, StefaniaLusa, SaraGazzano, ElenaSalzano, GiuseppinaPinzòn-Daza, Martha LeonorGiordano, AntonioDesiderio, VincenzoGhigo, DarioDe Rosa, GiuseppeCaraglia, MicheleRiganti, ChiaraKopecka, JoannaLusa, SaraPorto, StefaniaGazzano, ElenaSalzano, GiuseppinaPinzòn-Daza, Martha LeonorGiordano, AntonioDesiderio, VincenzoGhigo, DarioDe Rosa, GiuseppeCaraglia, MicheleRiganti, Chiaraa291e2ea-8de7-46e2-88bc-de62431360a36004554b473-1a7f-4b11-b11e-3e7603b8d5626002e727e28-9016-436e-b990-a3d4c44146c46007545c108-c972-4dce-8dc9-f74a8f94058e600cbb8aff0-59ff-4c25-ae5b-62b3dbf28cb6600d182f6d9-2e33-41b5-a076-a12c5be3a970600b592d2ed-3d84-4eae-bf8a-ddc1d267f00260041870e9c-426f-4120-a383-71a74ab6063660004bacc14-5fef-40a3-b500-a141b62bb0806008d432622-67f4-4c4d-aeb3-b55f335134396000b74591e-00fc-494e-b280-50aa3e4b8310600a7fb3fa7-8eb4-408c-874b-b3ebd111c3856002018-04-10T13:56:17Z2018-04-10T13:56:17Z20162016The resistance to chemotherapy and the tumor escape from host immunosurveillance are the main causes of the failure of anthracycline-based regimens in breast cancer, where an effective chemo-immunosensitizing strategy is lacking. The clinically used aminobisphosphonate zoledronic acid (ZA) reverses chemoresistance and immunoresistance in vitro. Previously we developed a nanoparticle-based zoledronic acid-containing formulation (NZ) that allowed a higher intratumor delivery of the drug compared with free ZA in vivo. We tested its efficacy in combination with doxorubicin in breast tumors refractory to chemotherapy and immune system recognition as a new combinatorial approach to produce chemo- and immunosensitization. NZ reduced the IC50 of doxorubicin in human and murine chemoresistant breast cancer cells and restored the doxorubicin efficacy against chemo-immunoresistant tumors implanted in immunocompetent mice. By reducing the metabolic flux through the mevalonate pathway, NZ lowered the activity of Ras/ERK1/2/HIF-1? axis and the expression of P-glycoprotein, decreased the glycolysis and the mitochondrial respiratory chain, induced a cytochrome c/caspase 9/caspase 3-dependent apoptosis, thus restoring the direct cytotoxic effects of doxorubicin on tumor cell. Moreover, NZ restored the doxorubicin-induced immunogenic cell death and reversed the tumorinduced immunosuppression due to the production of kynurenine, by inhibiting the STAT3/indoleamine 2,3 dioxygenase axis. These events increased the number of dendritic cells and decreased the number of immunosuppressive T-regulatory cells infiltrating the tumors. Our work proposes the use of nanoparticle encapsulating zoledronic acid as an effective tool overcoming at the same time chemoresistance and immunoresistance in breast tumors, thanks to the effects exerted on tumor cell and tumor-infiltrating immune cells.application/pdfISSN: 1949-2553http://repository.urosario.edu.co/handle/10336/17810eng20772No. 1220753OncotargetVol. 15Oncotarget, ISSN: 1949-2553, Vol. 15/No.12 (April 2016) pp. 20753-20772https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991490/Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURHipoxia De La CélulaNeoplasias Del Cuello UterinoCélulas EndotelialesMicroambiente TumoralCélulas HelaFactores De Transcripción StatEstrés FisiológicoEnfermedades616600Neoplasias de la MamaEpirrubicinaPontos QuânticosCélulas Tumorales CultivadasSelf-Assembling NanoparticlesZoledronic AcidDoxorubicin ResistanceImmunoresistanceImmunosuppressionZoledronic acid-encapsulating self-assembling nanoparticles and doxorubicin: a combinatorial approach to overcome simultaneously chemoresistance and immunoresistance in breast tumorsarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501ORIGINAL2.pdfapplication/pdf8228031https://repository.urosario.edu.co/bitstreams/d34c7241-3358-4156-be2c-202e4d4259e3/download9c966bfe894289da4f9dd16934546f91MD51TEXT2.pdf.txt2.pdf.txtExtracted texttext/plain81618https://repository.urosario.edu.co/bitstreams/2ae75bd7-01c3-42a2-966d-507ea3e3bd9d/downloade4112594df6fce4670f4bf3530744ca3MD52THUMBNAIL2.pdf.jpg2.pdf.jpgGenerated Thumbnailimage/jpeg5021https://repository.urosario.edu.co/bitstreams/c420dee0-faf6-4bca-9808-0c184e5aac2e/download6a8a88d5655c6b272872a70d6b746923MD5310336/17810oai:repository.urosario.edu.co:10336/178102019-09-19 07:38:03.190837https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |