Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer
- Autores
- Ding, Hui; Helguera, Gustavo Fernando; Rodríguez, José A.; Markman, Janet; Luria Pérez, Rosendo; Gangalum, Pallavi; Portilla Arias, Jose; Inoue, Satoshi; Daniels Wells, Tracy R.; Black, Keith; Holler, Eggehard; Penichet, Manuel L.; Ljubimova, Julia Y.
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Breast cancer remains the second leading cause of cancer death among women in the United States. Breast cancer prognosis is particularly poor in case of tumors overexpressing the oncoprotein HER2/neu. A new nanobioconjugate of the PolycefinTM family of anti-cancer drugs based on biodegradable and non-toxic polymalic acid (PMLA) was engineered for a multi-pronged attack on HER2/neu-positive breast cancer cells. An antibody-cytokine fusion protein consisting of the immunostimulatory cytokine interleukin-2 (IL-2) genetically fused to an antibody specific for human HER2/neu [anti-HER2/neu IgG3-(IL-2)] was covalently attached to the PMLA backbone to target HER2/neu expressing tumors and ensure the delivery of IL-2 to the tumor microenvironment. Antisense oligonucleotides (AON) were conjugated to the nanodrug to inhibit the expression of vascular tumor protein laminin-411 in order to block tumor angiogenesis. It is shown that the nanobioconjugate was capable of specifically binding human HER2/neu and retained the biological activity of IL-2. We also showed the uptake of the nanobioconjugate into HER2/neu-positive breast cancer cells and enhanced tumor targeting in vivo. The nanobioconjugate exhibited marked anti-tumor activity manifested by significantly longer animal survival and significantly increased anti-HER2/neu immune response in immunocompetent mice bearing D2F2/E2 murine mammary tumors that express human HER2/neu. The combination of laminin-411 AON and antibody-cytokine fusion protein on a single polymeric platform results in a new nanobioconjugate that can act against cancer cells through inhibition of tumor growth and angiogenesis and the orchestration of an immune response against the tumor. The present PolycefinTM variant may be a promising agent for treating HER2/neu expressing tumors and demonstrates the versatility of the PolycefinTM nanobioconjugate platform.
Fil: Ding, Hui. Cedars Sinai Medical Center;
Fil: Helguera, Gustavo Fernando. University of California at Los Angeles; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina
Fil: Rodríguez, José A.. University of California at Los Angeles; Estados Unidos
Fil: Markman, Janet. Cedars Sinai Medical Center;
Fil: Luria Pérez, Rosendo. University of California at Los Angeles; Estados Unidos
Fil: Gangalum, Pallavi. Cedars Sinai Medical Center;
Fil: Portilla Arias, Jose. Cedars Sinai Medical Center;
Fil: Inoue, Satoshi. Cedars Sinai Medical Center; . Saga University; Japón
Fil: Daniels Wells, Tracy R.. University of California at Los Angeles; Estados Unidos
Fil: Black, Keith. Cedars Sinai Medical Center;
Fil: Holler, Eggehard. Cedars Sinai Medical Center;
Fil: Penichet, Manuel L.. University of California at Los Angeles; Estados Unidos
Fil: Ljubimova, Julia Y.. Cedars Sinai Medical Center; - Materia
-
Polymalic Acid
Nanobioconjugate
Her2/Neu
Breast Cancer
Antibody-Il-2 Fusion Protein
Laminin-411 - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/26772
Ver los metadatos del registro completo
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Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancerDing, HuiHelguera, Gustavo FernandoRodríguez, José A.Markman, JanetLuria Pérez, RosendoGangalum, PallaviPortilla Arias, JoseInoue, SatoshiDaniels Wells, Tracy R.Black, KeithHoller, EggehardPenichet, Manuel L.Ljubimova, Julia Y.Polymalic AcidNanobioconjugateHer2/NeuBreast CancerAntibody-Il-2 Fusion ProteinLaminin-411https://purl.org/becyt/ford/3.4https://purl.org/becyt/ford/3Breast cancer remains the second leading cause of cancer death among women in the United States. Breast cancer prognosis is particularly poor in case of tumors overexpressing the oncoprotein HER2/neu. A new nanobioconjugate of the PolycefinTM family of anti-cancer drugs based on biodegradable and non-toxic polymalic acid (PMLA) was engineered for a multi-pronged attack on HER2/neu-positive breast cancer cells. An antibody-cytokine fusion protein consisting of the immunostimulatory cytokine interleukin-2 (IL-2) genetically fused to an antibody specific for human HER2/neu [anti-HER2/neu IgG3-(IL-2)] was covalently attached to the PMLA backbone to target HER2/neu expressing tumors and ensure the delivery of IL-2 to the tumor microenvironment. Antisense oligonucleotides (AON) were conjugated to the nanodrug to inhibit the expression of vascular tumor protein laminin-411 in order to block tumor angiogenesis. It is shown that the nanobioconjugate was capable of specifically binding human HER2/neu and retained the biological activity of IL-2. We also showed the uptake of the nanobioconjugate into HER2/neu-positive breast cancer cells and enhanced tumor targeting in vivo. The nanobioconjugate exhibited marked anti-tumor activity manifested by significantly longer animal survival and significantly increased anti-HER2/neu immune response in immunocompetent mice bearing D2F2/E2 murine mammary tumors that express human HER2/neu. The combination of laminin-411 AON and antibody-cytokine fusion protein on a single polymeric platform results in a new nanobioconjugate that can act against cancer cells through inhibition of tumor growth and angiogenesis and the orchestration of an immune response against the tumor. The present PolycefinTM variant may be a promising agent for treating HER2/neu expressing tumors and demonstrates the versatility of the PolycefinTM nanobioconjugate platform.Fil: Ding, Hui. Cedars Sinai Medical Center;Fil: Helguera, Gustavo Fernando. University of California at Los Angeles; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Rodríguez, José A.. University of California at Los Angeles; Estados UnidosFil: Markman, Janet. Cedars Sinai Medical Center;Fil: Luria Pérez, Rosendo. University of California at Los Angeles; Estados UnidosFil: Gangalum, Pallavi. Cedars Sinai Medical Center;Fil: Portilla Arias, Jose. Cedars Sinai Medical Center;Fil: Inoue, Satoshi. Cedars Sinai Medical Center; . Saga University; JapónFil: Daniels Wells, Tracy R.. University of California at Los Angeles; Estados UnidosFil: Black, Keith. Cedars Sinai Medical Center;Fil: Holler, Eggehard. Cedars Sinai Medical Center;Fil: Penichet, Manuel L.. University of California at Los Angeles; Estados UnidosFil: Ljubimova, Julia Y.. Cedars Sinai Medical Center;Elsevier Science2013-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/26772Ding, Hui; Helguera, Gustavo Fernando; Rodríguez, José A.; Markman, Janet; Luria Pérez, Rosendo; et al.; Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer; Elsevier Science; Journal of Controlled Release; 171; 3; 6-2013; 322-3290168-3659CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0168365913003350info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jconrel.2013.06.001info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:08:12Zoai:ri.conicet.gov.ar:11336/26772instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:08:12.413CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
title |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
spellingShingle |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer Ding, Hui Polymalic Acid Nanobioconjugate Her2/Neu Breast Cancer Antibody-Il-2 Fusion Protein Laminin-411 |
title_short |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
title_full |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
title_fullStr |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
title_full_unstemmed |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
title_sort |
Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer |
dc.creator.none.fl_str_mv |
Ding, Hui Helguera, Gustavo Fernando Rodríguez, José A. Markman, Janet Luria Pérez, Rosendo Gangalum, Pallavi Portilla Arias, Jose Inoue, Satoshi Daniels Wells, Tracy R. Black, Keith Holler, Eggehard Penichet, Manuel L. Ljubimova, Julia Y. |
author |
Ding, Hui |
author_facet |
Ding, Hui Helguera, Gustavo Fernando Rodríguez, José A. Markman, Janet Luria Pérez, Rosendo Gangalum, Pallavi Portilla Arias, Jose Inoue, Satoshi Daniels Wells, Tracy R. Black, Keith Holler, Eggehard Penichet, Manuel L. Ljubimova, Julia Y. |
author_role |
author |
author2 |
Helguera, Gustavo Fernando Rodríguez, José A. Markman, Janet Luria Pérez, Rosendo Gangalum, Pallavi Portilla Arias, Jose Inoue, Satoshi Daniels Wells, Tracy R. Black, Keith Holler, Eggehard Penichet, Manuel L. Ljubimova, Julia Y. |
author2_role |
author author author author author author author author author author author author |
dc.subject.none.fl_str_mv |
Polymalic Acid Nanobioconjugate Her2/Neu Breast Cancer Antibody-Il-2 Fusion Protein Laminin-411 |
topic |
Polymalic Acid Nanobioconjugate Her2/Neu Breast Cancer Antibody-Il-2 Fusion Protein Laminin-411 |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.4 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Breast cancer remains the second leading cause of cancer death among women in the United States. Breast cancer prognosis is particularly poor in case of tumors overexpressing the oncoprotein HER2/neu. A new nanobioconjugate of the PolycefinTM family of anti-cancer drugs based on biodegradable and non-toxic polymalic acid (PMLA) was engineered for a multi-pronged attack on HER2/neu-positive breast cancer cells. An antibody-cytokine fusion protein consisting of the immunostimulatory cytokine interleukin-2 (IL-2) genetically fused to an antibody specific for human HER2/neu [anti-HER2/neu IgG3-(IL-2)] was covalently attached to the PMLA backbone to target HER2/neu expressing tumors and ensure the delivery of IL-2 to the tumor microenvironment. Antisense oligonucleotides (AON) were conjugated to the nanodrug to inhibit the expression of vascular tumor protein laminin-411 in order to block tumor angiogenesis. It is shown that the nanobioconjugate was capable of specifically binding human HER2/neu and retained the biological activity of IL-2. We also showed the uptake of the nanobioconjugate into HER2/neu-positive breast cancer cells and enhanced tumor targeting in vivo. The nanobioconjugate exhibited marked anti-tumor activity manifested by significantly longer animal survival and significantly increased anti-HER2/neu immune response in immunocompetent mice bearing D2F2/E2 murine mammary tumors that express human HER2/neu. The combination of laminin-411 AON and antibody-cytokine fusion protein on a single polymeric platform results in a new nanobioconjugate that can act against cancer cells through inhibition of tumor growth and angiogenesis and the orchestration of an immune response against the tumor. The present PolycefinTM variant may be a promising agent for treating HER2/neu expressing tumors and demonstrates the versatility of the PolycefinTM nanobioconjugate platform. Fil: Ding, Hui. Cedars Sinai Medical Center; Fil: Helguera, Gustavo Fernando. University of California at Los Angeles; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina Fil: Rodríguez, José A.. University of California at Los Angeles; Estados Unidos Fil: Markman, Janet. Cedars Sinai Medical Center; Fil: Luria Pérez, Rosendo. University of California at Los Angeles; Estados Unidos Fil: Gangalum, Pallavi. Cedars Sinai Medical Center; Fil: Portilla Arias, Jose. Cedars Sinai Medical Center; Fil: Inoue, Satoshi. Cedars Sinai Medical Center; . Saga University; Japón Fil: Daniels Wells, Tracy R.. University of California at Los Angeles; Estados Unidos Fil: Black, Keith. Cedars Sinai Medical Center; Fil: Holler, Eggehard. Cedars Sinai Medical Center; Fil: Penichet, Manuel L.. University of California at Los Angeles; Estados Unidos Fil: Ljubimova, Julia Y.. Cedars Sinai Medical Center; |
description |
Breast cancer remains the second leading cause of cancer death among women in the United States. Breast cancer prognosis is particularly poor in case of tumors overexpressing the oncoprotein HER2/neu. A new nanobioconjugate of the PolycefinTM family of anti-cancer drugs based on biodegradable and non-toxic polymalic acid (PMLA) was engineered for a multi-pronged attack on HER2/neu-positive breast cancer cells. An antibody-cytokine fusion protein consisting of the immunostimulatory cytokine interleukin-2 (IL-2) genetically fused to an antibody specific for human HER2/neu [anti-HER2/neu IgG3-(IL-2)] was covalently attached to the PMLA backbone to target HER2/neu expressing tumors and ensure the delivery of IL-2 to the tumor microenvironment. Antisense oligonucleotides (AON) were conjugated to the nanodrug to inhibit the expression of vascular tumor protein laminin-411 in order to block tumor angiogenesis. It is shown that the nanobioconjugate was capable of specifically binding human HER2/neu and retained the biological activity of IL-2. We also showed the uptake of the nanobioconjugate into HER2/neu-positive breast cancer cells and enhanced tumor targeting in vivo. The nanobioconjugate exhibited marked anti-tumor activity manifested by significantly longer animal survival and significantly increased anti-HER2/neu immune response in immunocompetent mice bearing D2F2/E2 murine mammary tumors that express human HER2/neu. The combination of laminin-411 AON and antibody-cytokine fusion protein on a single polymeric platform results in a new nanobioconjugate that can act against cancer cells through inhibition of tumor growth and angiogenesis and the orchestration of an immune response against the tumor. The present PolycefinTM variant may be a promising agent for treating HER2/neu expressing tumors and demonstrates the versatility of the PolycefinTM nanobioconjugate platform. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/26772 Ding, Hui; Helguera, Gustavo Fernando; Rodríguez, José A.; Markman, Janet; Luria Pérez, Rosendo; et al.; Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer; Elsevier Science; Journal of Controlled Release; 171; 3; 6-2013; 322-329 0168-3659 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/26772 |
identifier_str_mv |
Ding, Hui; Helguera, Gustavo Fernando; Rodríguez, José A.; Markman, Janet; Luria Pérez, Rosendo; et al.; Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer; Elsevier Science; Journal of Controlled Release; 171; 3; 6-2013; 322-329 0168-3659 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0168365913003350 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jconrel.2013.06.001 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Science |
publisher.none.fl_str_mv |
Elsevier Science |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1842270035276464128 |
score |
13.13397 |