Myocardial matrix remodeling and the matrix metalloproteinases: influence on cardiac form and function.
By Francis G. Spinale. Physiological Reviews, 2007
1,136 citations recorded by the source corpus.
Subfields: Cancer Research, Cardiology and Cardiovascular Medicine, Oncology
View Paper: https://www.semanticscholar.org/paper/e45cfd17dc13d8bca143d456a84a293c552f5d19
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In Cancer Research
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Citations in the corpus
- Doxorubicin-induced cardiomyopathy: from molecular mechanisms to therapeutic strategies. (2012, background): “Significant alterations in the structure and composition of the extracellular matrix contribute to the development of heart failure [100].”
- Cellular Mechanotransduction: From Tension to Function (2018, background): “Following a cardiovascular event (ischemic insult, long term exposure to pressure or volume overload), cardiac matrix is degraded and substituted by a scar, having a different nanostructure and compliance (Spinale, 2007).”
- Cardiac fibrosis. (2020, background): “Resident cardiac fibroblasts may serve to maintain the structural integrity of the matrix network,(16) regulating collagen turnover, a process that requires ongoing synthesis and degradation of ECM proteins.(17,18) Fibroblast-specific baseline activation of Smad3 signal-”
- Pathological Ventricular Remodeling: Mechanisms: Part 1 of 2 (2013, background): “This surplus extracellular matrix, which constitutes scar or fibrosis, promotes both contractile dysfunction and rhythm disturbances.(84) As a result, cardiac fibrosis contributes to morbidity and mortality in many forms of heart disease.”
- The Pathogenesis of Cardiac Fibrosis (2013, neutral): “Homeostatic control of the cardiac extracellular matrix involves ongoing synthesis and degradation of matrix proteins [17, 18].”
- Upregulation of ADAMTS-7 and downregulation of COMP are associated with aortic aneurysm (2017, positive): “A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS), belonging to the metalloproteinase family, is important in bone formation and arterial/cardiac remodeling (2-4).”
- Cardiac fibroblasts, fibrosis and extracellular matrix remodeling in heart disease (2012, background): “Among the 26 MMPs cloned and characterized in vertebrates, the MMPs so far identified to be involved in myocardial remodeling are as follows: MMP1, MMP3, MMP8, MMP13, MMP2, MMP9, MMP12, MMP28 and the membrane-type MMPs (MT1-MMP/MMP14) [65-69], although the role of higher MMPs in the cardiovascular s”