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dc.contributor.authorLejeune, M.*
dc.contributor.authorReverté, L.*
dc.contributor.authorGallardo, N.*
dc.contributor.authorSauras, E.*
dc.contributor.authorBosch, R.*
dc.contributor.authorMata, D.*
dc.contributor.authorRoso, A.*
dc.contributor.authorPetit, A.*
dc.contributor.authorPeg, V.*
dc.contributor.authorRiu, F.*
dc.contributor.authorGarcía-Fontgivell, J.*
dc.contributor.authorRelea, F.*
dc.contributor.authorVieites Pérez-Quintela, María Begoña *
dc.contributor.authorde la Cruz-Merino, L.*
dc.contributor.authorArenas, M.*
dc.contributor.authorRodriguez, V.*
dc.contributor.authorGalera, J.*
dc.contributor.authorKorzynska, A.*
dc.contributor.authorPlancoulaine, B.*
dc.contributor.authorÁlvaro, T.*
dc.contributor.authorLópez, C.*
dc.date.accessioned2025-09-10T08:43:31Z
dc.date.available2025-09-10T08:43:31Z
dc.date.issued2023
dc.identifier.citationLejeune M, Reverté L, Gallardo N, Sauras E, Bosch R, Mata D, et al. Matrix Metalloproteinase-9 Expression Is Associated with the Absence of Response to Neoadjuvant Chemotherapy in Triple-Negative Breast Cancer Patients. International Journal of Molecular Sciences. 2023;24(14).
dc.identifier.issn1422-0067
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/64e2a6504a4f093d56e74315
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21723
dc.description.abstractTriple-negative breast cancer (TNBC) is particularly challenging due to the weak or absent response to therapeutics and its poor prognosis. The effectiveness of neoadjuvant chemotherapy (NAC) response is strongly influenced by changes in elements of the tumor microenvironment (TME). This work aimed to characterize the residual TME composition in 96 TNBC patients using immunohistochemistry and in situ hybridization techniques and evaluate its prognostic implications for partial responders vs. non-responders. Compared with non-responders, partial responders containing higher levels of CD83+ mature dendritic cells, FOXP3+ regulatory T cells, and IL-15 expression but lower CD138+ cell concentration exhibited better OS and RFS. However, along with tumor diameter and positive nodal status at diagnosis, matrix metalloproteinase-9 (MMP-9) expression in the residual TME was identified as an independent factor associated with the impaired response to NAC. This study yields new insights into the key components of the residual tumor bed, such as MMP-9, which is strictly associated with the lack of a pathological response to NAC. This knowledge might help early identification of TNBC patients less likely to respond to NAC and allow the establishment of new therapeutic targets.
dc.description.sponsorshipThis research was supported by grants from the Instituto de Salud Carlos III (PI13/02501 and PI11/0488) co-financed by the European Regional Development Fund (ERDF). ML acknowledges support from the PATH-IMAGE project, which was funded by ERDF (agreement 2903/335-41).
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshHumans *
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols *
dc.subject.meshMatrix Metalloproteinase 9 *
dc.subject.meshNeoadjuvant Therapy *
dc.subject.meshNeoplasm, Residual*
dc.subject.meshTriple Negative Breast Neoplasms *
dc.subject.meshTumor Microenvironment *
dc.titleMatrix Metalloproteinase-9 Expression Is Associated with the Absence of Response to Neoadjuvant Chemotherapy in Triple-Negative Breast Cancer Patients
dc.typeArtigo
dc.authorsophosLejeune, M.; Reverté, L.; Gallardo, N.; Sauras, E.; Bosch, R.; Mata, D.; Roso, A.; Petit, A.; Peg, V.; Riu, F.; García-Fontgivell, J.; Relea, F.; Vieites, B.; de la Cruz-Merino, L.; Arenas, M.; Rodriguez, V.; Galera, J.; Korzynska, A.; Plancoulaine, B.; Álvaro, T.; López, C.
dc.identifier.doi10.3390/ijms241411297
dc.identifier.sophos64e2a6504a4f093d56e74315
dc.issue.number14
dc.journal.titleInternational Journal of Molecular Sciences*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Hospital Público de Monforte::Anatomía patolóxia
dc.relation.projectIDInstituto de Salud Carlos III [PI13/02501, PI11/0488]
dc.relation.projectIDEuropean Regional Development Fund (ERDF) [2903/335-41]
dc.relation.projectIDPATH-IMAGE
dc.relation.publisherversionhttps://doi.org/10.3390/ijms241411297
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Lugo
dc.subject.keywordHP Monforte
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number24


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)