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                  <mods:namePart>Morcillo, Miguel Ángel</mods:namePart>
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                  <mods:namePart>Martinez Torrecuadrada, Jorge Luis</mods:namePart>
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               <mods:name>
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                  <mods:dateAccessioned encoding="iso8601">2018-11-21T12:56:19Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Contrast Media Mol Imaging. 2018; 2018:8382148.</mods:identifier>
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               <mods:identifier type="e-issn">1555-4317</mods:identifier>
               <mods:identifier type="issn">1555-4309</mods:identifier>
               <mods:identifier type="journal">Contrast media &amp; molecular imaging</mods:identifier>
               <mods:identifier type="pubmedID">30224904</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/6658</mods:identifier>
               <mods:abstract>Pancreatic ductal adenocarcinoma (PDAC) continues to be one of the deadliest cancers for which optimal diagnostic tools are still greatly needed. Identification of PDAC-specific molecular markers would be extremely useful to improve disease diagnosis and follow-up. MT1-MMP has long been involved in pancreatic cancer, especially in tumour invasion and metastasis. In this study, we aim to ascertain the suitability of MT1-MMP as a biomarker for positron emission tomography (PET) imaging. Two probes were assessed and compared for this purpose, an MT1-MMP-specific binding peptide (MT1-AF7p) and a specific antibody (LEM2/15), labelled, respectively, with 68Ga and with 89Zr. PET imaging with both probes was conducted in patient-derived xenograft (PDX), subcutaneous and orthotopic, PDAC mouse models, and in a cancer cell line (CAPAN-2)-derived xenograft (CDX) model. Both radiolabelled tracers were successful in identifying, by means of PET imaging techniques, tumour tissues expressing MT1-MMP although they did so at different uptake levels. The 89Zr-DFO-LEM2/15 probe showed greater specific activity compared to the 68Ga-labelled peptide. The mean value of tumour uptake for the 89Zr-DFO-LEM2/15 probe (5.67 ± 1.11%ID/g, n=28) was 25-30 times higher than that of the 68Ga-DOTA-AF7p ones. Tumour/blood ratios (1.13 ± 0.51 and 1.44 ± 0.43 at 5 and 7 days of 89Zr-DFO-LEM2/15 after injection) were higher than those estimated for 68Ga-DOTA-AF7p probes (of approximately tumour/blood ratio = 0.5 at 90 min after injection). Our findings strongly point out that (i) the in vivo detection of MT1-MMP by PET imaging is a promising strategy for PDAC diagnosis and (ii) labelled LEM2/15 antibody is a better candidate than MT1-AF7p for PDAC detection.</mods:abstract>
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               <mods:subject>
                  <mods:topic>P-ISOTHIOCYANATOBENZYL-DESFERRIOXAMINE</mods:topic>
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               <mods:subject>
                  <mods:topic>TYPE-1 MATRIX-METALLOPROTEINASE</mods:topic>
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               <mods:subject>
                  <mods:topic>IN-VIVO</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>MONOCLONAL-ANTIBODIES</mods:topic>
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               <mods:subject>
                  <mods:topic>BIFUNCTIONAL CHELATE</mods:topic>
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                  <mods:topic>TUMOR-GROWTH</mods:topic>
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               <mods:titleInfo>
                  <mods:title>MT1-MMP as a PET Imaging Biomarker for Pancreas Cancer Management</mods:title>
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