| Literature DB >> 25562641 |
Marcus Franz1, Christian Jung, Alexander Lauten, Hans R Figulla, Alexander Berndt.
Abstract
Fetal variants of tenascin-C are not expressed in healthy adult myocardium. But, there is a relevant re-occurrence during pathologic cardiac tissue and vascular remodeling. Thus, these molecules, in particular B and C domain containing tenascin-C, might qualify as promising novel biomarkers for diagnosis and prognosis estimation. Since a stable extracellular deposition of fetal tenascin-C variants is present in diseased cardiac tissue, the molecules are excellent target structures for antibody-based delivery of diagnostic (e.g., radionuclides) or therapeutic (bioactive payloads) agents directly to the site of disease. Against the background that fetal tenascin-C variants are functionally involved in cardiovascular tissue remodeling, therapeutic functional blocking strategies could be experimentally tested in the future.Entities:
Keywords: cardiovascular diseases; diagnosis; prognosis; tenascin-C; therapy
Mesh:
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Year: 2015 PMID: 25562641 PMCID: PMC4422793 DOI: 10.1080/19336918.2014.1000075
Source DB: PubMed Journal: Cell Adh Migr ISSN: 1933-6918 Impact factor: 3.405