<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T06:46:17Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/10120" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/10120</identifier><datestamp>2025-10-24T10:44:02Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Matrix Metalloproteinase-9 Expression Is Associated with the Absence of Response to Neoadjuvant Chemotherapy in Triple-Negative Breast Cancer Patients</dc:title>
   <dc:creator>Lejeune, Marylène</dc:creator>
   <dc:creator>Reverté Calvet, Laia</dc:creator>
   <dc:creator>Gallardo Borràs, Noèlia</dc:creator>
   <dc:creator>Sauras-Colón, Esther</dc:creator>
   <dc:creator>Bosch Príncep, Ramon</dc:creator>
   <dc:creator>Mata Cano, Daniel</dc:creator>
   <dc:creator>Peg, Vicente</dc:creator>
   <dc:subject>Mama - Càncer - Tractament</dc:subject>
   <dc:subject>Medicaments antineoplàstics - Ús terapèutic</dc:subject>
   <dc:subject>DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms::Triple Negative Breast Neoplasms</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Combined Modality Therapy::Neoadjuvant Therapy</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama::neoplasias de mama triple negativos</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::tratamiento combinado::tratamiento neoadyuvante</dc:subject>
   <dcterms:abstract>Biomarkers; Neoadjuvant chemotherapy; Triple-negative breast cancer</dcterms:abstract>
   <dcterms:abstract>Biomarcadores; Quimioterapia neoadyuvante; Cáncer de mama triple negativo</dcterms:abstract>
   <dcterms:abstract>Biomarcadors; Quimioteràpia neoadjuvant; Càncer de mama triple negatiu</dcterms:abstract>
   <dcterms:abstract>Triple-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.</dcterms:abstract>
   <dcterms:abstract>This 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).</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:44:02Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:44:02Z</dcterms:available>
   <dcterms:created>2025-10-24T10:44:02Z</dcterms:created>
   <dcterms:issued>2023-08-22T12:53:04Z</dcterms:issued>
   <dcterms:issued>2023-08-22T12:53:04Z</dcterms:issued>
   <dcterms:issued>2023-07-11</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/10120</dc:identifier>
   <dc:relation>International Journal of Molecular Sciences;24(14)</dc:relation>
   <dc:relation>https://doi.org/10.3390/ijms241411297</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>MDPI</dc:publisher>
   <dc:source>Scientia</dc:source>
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