<?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>2026-06-28T20:28:24Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/116227" metadataPrefix="qdc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/116227</identifier><datestamp>2025-03-18T14:51:02Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</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>Clinical relevance of MMP-9, MMP-2, TIMP-1 and TIMP-2 in colorectal cancer</dc:title>
   <dc:creator>Morán, Alberto</dc:creator>
   <dc:creator>García-Aranda, Carmen</dc:creator>
   <dc:creator>Díaz-López, Antonio</dc:creator>
   <dc:creator>Iniesta Serrano, María Pilar</dc:creator>
   <dc:creator>Juan Chocano, María Del Carmen De</dc:creator>
   <dc:creator>Sánchez Pernaute, Andrés</dc:creator>
   <dc:creator>Torres García, Antonio José</dc:creator>
   <dc:creator>Díaz-Rubio García, Eduardo</dc:creator>
   <dc:creator>Balibrea Cantero, José Luis</dc:creator>
   <dc:creator>Benito De Las Heras, Manuel R.</dc:creator>
   <dcterms:abstract>The main aim of this study was to evaluate the clinical relevance of Gelatinases in colorectal cancer (CRC). Ninety-five CRCs and their paired normal tissues were investigated to detect total levels of MMP-9, MMP-2, and the tissue inhibitors TIMP-1 and TIMP-2. Also, pro-MMP and MMP activity, and potential associations with clinical parameters were estimated. MMP-9, MMP-2 and TIMP-1 levels were greater in CRCs than in normal tissues, differences being significant for MMP-9 and TIMP-1. However, TIMP-2 showed significantly lower levels in tumour samples. Moreover, significant differences in the state of activation between gelatinases were found. TIMP-1 low levels were significantly associated with poor clinical outcome of patients. According to these data, different roles have to be attributed to MMP-2 and MMP-9 in CRC progression. Moreover, TIMP-1 level evaluation emerges as the main prognostic factor in relation to Gelatinases A and B activity in CRC.</dcterms:abstract>
   <dcterms:dateAccepted>2025-01-27T11:09:52Z</dcterms:dateAccepted>
   <dcterms:available>2025-01-27T11:09:52Z</dcterms:available>
   <dcterms:created>2025-01-27T11:09:52Z</dcterms:created>
   <dcterms:issued>2005</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/116227</dc:identifier>
   <dc:identifier>1021-335X</dc:identifier>
   <dc:identifier>10.3892/or.13.1.115</dc:identifier>
   <dc:identifier>1791-2431</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Morán A, Iniesta P, García-Aranda C, De Juan C, Díaz-López A, Sánchez- Pernaute A, Torres AJ, Díaz-Rubio E, Balibrea JL, Benito M. Clinical relevance of MMP-9, MMP-2, TIMP-1 and TIMP-2 in colorectal cancer. Oncol Rep. 2005 Jan;13(1):115-20. PMID: 15583811.</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>restricted access</dc:rights>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:publisher>SPANDIDOS PUBL LTD</dc:publisher>
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