Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer

Autores
Marchesini, Abril; Gómez Bergna, Santiago Manuel; Amorós Morales, Leslie Cinthya; López, María Florencia; Vásquez, Larisa; Tongiani, Silvana E.; González Morán, Florencia; Romanowski, Víctor; Gottardo, María Florencia; Pidre, Matías Luis
Año de publicación
2025
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
BIRC6, a member of the inhibitor of apoptosis protein family (IAP), regulates apoptosis, autophagy and cytokinesis. IAPs are often overexpressed in tumors, contributing to oncogenesis, therapy resistance and worse prognosis. In particular, BIRC6 overexpression has been found in several tumor tissues. The aim of this study was to evaluate the effect of BIRC6 silencing on the apoptotic response of breast and lung tumor cells. We used RNA interference based on short hairpin RNA (shRNA) to knock down gene expression encoded by a recombinant baculovirus (BV), an insect-specific virus unable to replicate in mammalian hosts, to carry out preclinical validation tests in experimental models both in vitro and in vivo. Our results indicate that BIRC6 plays an antiapoptotic role in both breast and lung tumor cells. In vivo, treatment with BV-shBRIC6 reduced breast and lung tumor progression and increased overall survival. After histological analysis, BV-shBRIC6 was able to increase tumor necrosis. In addition, we demonstrated that BIRC6 expression correlates with antiapoptotic and tumor progression-relevant markers in lung and breast cancer patients. BV-based silencing of BIRC6 may have therapeutic value for the treatment of lung and breast tumors. Further translational studies of BV-shBIRC6 in lung and breast cancer are warranted.
Instituto de Biotecnología y Biología Molecular
Materia
Biología
BIRC6
baculovirus
shRNA
lung cancer
breast cancer
apoptosis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/189345

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network_name_str SEDICI (UNLP)
spelling Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast CancerMarchesini, AbrilGómez Bergna, Santiago ManuelAmorós Morales, Leslie CinthyaLópez, María FlorenciaVásquez, LarisaTongiani, Silvana E.González Morán, FlorenciaRomanowski, VíctorGottardo, María FlorenciaPidre, Matías LuisBiologíaBIRC6baculovirusshRNAlung cancerbreast cancerapoptosisBIRC6, a member of the inhibitor of apoptosis protein family (IAP), regulates apoptosis, autophagy and cytokinesis. IAPs are often overexpressed in tumors, contributing to oncogenesis, therapy resistance and worse prognosis. In particular, BIRC6 overexpression has been found in several tumor tissues. The aim of this study was to evaluate the effect of BIRC6 silencing on the apoptotic response of breast and lung tumor cells. We used RNA interference based on short hairpin RNA (shRNA) to knock down gene expression encoded by a recombinant baculovirus (BV), an insect-specific virus unable to replicate in mammalian hosts, to carry out preclinical validation tests in experimental models both in vitro and in vivo. Our results indicate that BIRC6 plays an antiapoptotic role in both breast and lung tumor cells. In vivo, treatment with BV-shBRIC6 reduced breast and lung tumor progression and increased overall survival. After histological analysis, BV-shBRIC6 was able to increase tumor necrosis. In addition, we demonstrated that BIRC6 expression correlates with antiapoptotic and tumor progression-relevant markers in lung and breast cancer patients. BV-based silencing of BIRC6 may have therapeutic value for the treatment of lung and breast tumors. Further translational studies of BV-shBIRC6 in lung and breast cancer are warranted.Instituto de Biotecnología y Biología Molecular2025-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/189345enginfo:eu-repo/semantics/altIdentifier/issn/1999-4915info:eu-repo/semantics/altIdentifier/doi/10.3390/v17111458info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2026-01-07T13:36:23Zoai:sedici.unlp.edu.ar:10915/189345Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292026-01-07 13:36:24.302SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
title Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
spellingShingle Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
Marchesini, Abril
Biología
BIRC6
baculovirus
shRNA
lung cancer
breast cancer
apoptosis
title_short Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
title_full Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
title_fullStr Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
title_full_unstemmed Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
title_sort Baculovirus-Mediated Gene Therapy: Targeting BIRC6 for Lung and Breast Cancer
dc.creator.none.fl_str_mv Marchesini, Abril
Gómez Bergna, Santiago Manuel
Amorós Morales, Leslie Cinthya
López, María Florencia
Vásquez, Larisa
Tongiani, Silvana E.
González Morán, Florencia
Romanowski, Víctor
Gottardo, María Florencia
Pidre, Matías Luis
author Marchesini, Abril
author_facet Marchesini, Abril
Gómez Bergna, Santiago Manuel
Amorós Morales, Leslie Cinthya
López, María Florencia
Vásquez, Larisa
Tongiani, Silvana E.
González Morán, Florencia
Romanowski, Víctor
Gottardo, María Florencia
Pidre, Matías Luis
author_role author
author2 Gómez Bergna, Santiago Manuel
Amorós Morales, Leslie Cinthya
López, María Florencia
Vásquez, Larisa
Tongiani, Silvana E.
González Morán, Florencia
Romanowski, Víctor
Gottardo, María Florencia
Pidre, Matías Luis
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Biología
BIRC6
baculovirus
shRNA
lung cancer
breast cancer
apoptosis
topic Biología
BIRC6
baculovirus
shRNA
lung cancer
breast cancer
apoptosis
dc.description.none.fl_txt_mv BIRC6, a member of the inhibitor of apoptosis protein family (IAP), regulates apoptosis, autophagy and cytokinesis. IAPs are often overexpressed in tumors, contributing to oncogenesis, therapy resistance and worse prognosis. In particular, BIRC6 overexpression has been found in several tumor tissues. The aim of this study was to evaluate the effect of BIRC6 silencing on the apoptotic response of breast and lung tumor cells. We used RNA interference based on short hairpin RNA (shRNA) to knock down gene expression encoded by a recombinant baculovirus (BV), an insect-specific virus unable to replicate in mammalian hosts, to carry out preclinical validation tests in experimental models both in vitro and in vivo. Our results indicate that BIRC6 plays an antiapoptotic role in both breast and lung tumor cells. In vivo, treatment with BV-shBRIC6 reduced breast and lung tumor progression and increased overall survival. After histological analysis, BV-shBRIC6 was able to increase tumor necrosis. In addition, we demonstrated that BIRC6 expression correlates with antiapoptotic and tumor progression-relevant markers in lung and breast cancer patients. BV-based silencing of BIRC6 may have therapeutic value for the treatment of lung and breast tumors. Further translational studies of BV-shBIRC6 in lung and breast cancer are warranted.
Instituto de Biotecnología y Biología Molecular
description BIRC6, a member of the inhibitor of apoptosis protein family (IAP), regulates apoptosis, autophagy and cytokinesis. IAPs are often overexpressed in tumors, contributing to oncogenesis, therapy resistance and worse prognosis. In particular, BIRC6 overexpression has been found in several tumor tissues. The aim of this study was to evaluate the effect of BIRC6 silencing on the apoptotic response of breast and lung tumor cells. We used RNA interference based on short hairpin RNA (shRNA) to knock down gene expression encoded by a recombinant baculovirus (BV), an insect-specific virus unable to replicate in mammalian hosts, to carry out preclinical validation tests in experimental models both in vitro and in vivo. Our results indicate that BIRC6 plays an antiapoptotic role in both breast and lung tumor cells. In vivo, treatment with BV-shBRIC6 reduced breast and lung tumor progression and increased overall survival. After histological analysis, BV-shBRIC6 was able to increase tumor necrosis. In addition, we demonstrated that BIRC6 expression correlates with antiapoptotic and tumor progression-relevant markers in lung and breast cancer patients. BV-based silencing of BIRC6 may have therapeutic value for the treatment of lung and breast tumors. Further translational studies of BV-shBIRC6 in lung and breast cancer are warranted.
publishDate 2025
dc.date.none.fl_str_mv 2025-10
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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http://purl.org/coar/resource_type/c_6501
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status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/189345
url http://sedici.unlp.edu.ar/handle/10915/189345
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1999-4915
info:eu-repo/semantics/altIdentifier/doi/10.3390/v17111458
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
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reponame_str SEDICI (UNLP)
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instname_str Universidad Nacional de La Plata
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repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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