摘要:
The present invention describes the method for determining the risk of future major adverse cardiovascular events, which comprises detection proteolytic fragments of IGFBP-4 or IGFBP-5 (insulin-like growth factor binding protein 4 or insulin-like growth factor binding protein 5) in patients' blood. The present invention provides antibodies and immunoas-says, suitable for specific measurement of proteolytic fragments of IGFBPs. In current invention the IGFBP fragments are suggested to be utilized as blood biomarkers for the risk prediction of major adverse cardiovascular events (MACE).
摘要:
Compositions comprising IGFBP-3 receptor agonists and methods for the treatment of metabolic syndrome, obstructive respiratory disorders, obstructive or inflammatory respiratory disease, cancers and related diseases with IGFBP-3 receptor agonists are presented. A method for interfering with the activity of nuclear factor-kappaB (NF-KB) in a cell, comprising: providing to a cell an effective amount of a composition comprising an IGFBP-3 receptor agonist; and interfering with the activity of NF-KB in the cell is included.
摘要:
It is an object of the present invention to provide methods and compositions for protection of subjects from acute kidney injury by treating the subject with compounds that modulate the cell cycle. Modulating the cell cycle can comprise inducing G 0 /G 1 cell cycle arrest, and/or inducing cell cycle progression. As demonstrated below, even a single administration of a compound which induces G 0 /G 1 cell cycle arrest can protect subjects from AKI, and may be used prophylactically in advance of, or as a treatment following, various treatments or conditions that are known to be injurious to the kidney, followed optionally by release of the arrest. Once AKI is established, cell cycle progression can be induced to increase replacement of lost and damaged cells.
摘要:
The invention concerns the use of a protein characterized in that it comprises or consists of the NOV protein, represented by the sequence SEQ ID NO: 2, or a fragment of said protein, provided that said fragment exhibits an angiogenesis inhibiting activity, or any sequence derived from the sequence SEQ ID NO: 2 or a fragment as defined above, provided that said derived sequence exhibits an angiogenesis inhibiting activity, or any sequence homologous of the sequence SEQ ID NO: 2 or a fragment as defined above, provided that said homologous sequence exhibits an angiogenesis inhibiting activity, for preparing a medicine for treating pathologies requiring inhibition of endothelial proliferation or pathologies requiring inhibition of endothelial activation.
摘要:
The invention provides a therapeutic composition for epithelial wound repair that is a combination of PDGF and KGF. Further, the invention provides a composition for epithelial wound repair that is a therapeutic combination of PDGF, KGF and IGF. Additionally, the invention provides a therapeutic composition of PDGF, KGF, IGF and IGFBP for epithelial wound repair.
摘要:
This invention relates to a pharmaceutical preparation comprising a combination of one or several receptor/binding proteins (binding growth factors or hormones) and hyaluronic acid (or its derivatives) or a biodegradable polymer, optionally in combination with its/their ligands (growth factors and hormones).
摘要:
The invention provides a therapeutic composition for epithelial wound repair that is a combination of PDGF and KGF. Further, the invention provides a composition for epithelial wound repair that is a therapeutic combination of PDGF, KGF and IGF. Additionally, the invention provides a therapeutic composition of PDGF, KGF, IGF and IGFBP for epithelial wound repair.