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                  <mods:namePart>González-Santamaría, José</mods:namePart>
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                  <mods:namePart>Comunidad de Madrid (España)</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Unión Europea. Comisión Europea</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2019-07-29T14:48:47Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Cardiovasc Res. 2016; 109(1):67-78</mods:identifier>
               <mods:identifier type="doi">10.1093/cvr/cvv214</mods:identifier>
               <mods:identifier type="e-issn">1755-3245</mods:identifier>
               <mods:identifier type="issn">0008-6363</mods:identifier>
               <mods:identifier type="journal">Cardiovascular research</mods:identifier>
               <mods:identifier type="pubmedID">26260798</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/7985</mods:identifier>
               <mods:abstract>AIMS: After myocardial infarction (MI), extensive remodelling of the extracellular matrix contributes to scar formation. While aiming to preserve tissue integrity, this fibrotic response is also associated with adverse events, including a markedly increased risk of heart failure, ventricular arrhythmias, and sudden cardiac death. Cardiac fibrosis is characterized by extensive deposition of collagen and also by increased stiffness as a consequence of enhanced collagen cross-linking. Members of the lysyl oxidase (LOX) family of enzymes are responsible for the formation of collagen cross-links. This study investigates the contribution of LOX family members to the heart response to MI. METHODS AND RESULTS: Experimental MI was induced in C57BL/6 mice by permanent ligation of the left anterior descending coronary artery. The expression of LOX isoforms (LOX and LOXL1-4) was strongly increased upon MI, and this response was accompanied by a significant accumulation of mature collagen fibres in the infarcted area. LOX expression was observed in areas of extensive remodelling, partially overlapping with α-smooth muscle actin-expressing myofibroblasts. Tumour growth factor-β as well as hypoxia-activated pathways contributed to the induction of LOX expression in cardiac fibroblasts. Finally, in vivo post-infarction treatment with the broadband LOX inhibitor β-aminopropionitrile or, selectively, with a neutralizing antibody against the canonical LOX isoform attenuated collagen accumulation and maturation and also resulted in reduced ventricular dilatation and improved cardiac function. CONCLUSION: LOX family members contribute significantly to the detrimental effects of cardiac remodelling, highlighting LOX inhibition as a potential therapeutic strategy for post-infarction recovery.</mods:abstract>
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                  <mods:topic>Cardiac fibrosis</mods:topic>
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                  <mods:topic>Collagen</mods:topic>
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               <mods:subject>
                  <mods:topic>Lysyl oxidases</mods:topic>
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               <mods:subject>
                  <mods:topic>Myocardial infarction</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Myofibroblast</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Matrix cross-linking lysyl oxidases are induced in response to myocardial infarction and promote cardiac dysfunction</mods:title>
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