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Recent insights into the actions of IGFBP-6
- Source :
- Journal of Cell Communication and Signaling. 9:189-200
- Publication Year :
- 2015
- Publisher :
- Springer Science and Business Media LLC, 2015.
-
Abstract
- IGFBP-6 is an O-linked glycoprotein that preferentially binds IGF-II over IGF-I. It is a relatively selective inhibitor of IGF-II actions including proliferation, survival and differentiation of a wide range of cells. IGFBP-6 has recently been shown to have a number of IGF-independent actions, including promotion of apoptosis in some cells and inhibition of angiogenesis. IGFBP-6 also induces migration of tumour cells including rhabdomyosarcomas by an IGF-independent mechanism. This chemotactic effect is mediated by MAP kinases. IGFBP-6 binds to prohibitin-2 on the cell surface and the latter is required for IGFBP-6-induced migration by a mechanism that is independent of MAP kinases. IGFBP-6 may enter the nucleus and modulate cell survival and differentiation. IGFBP-6 expression is decreased in a number of cancer cells and it has been postulated to act as a tumour suppressor. IGFBP-6 expression is increased in a smaller number of cancers, which may reflect a compensatory mechanism to control IGF-II actions or IGF-independent actions. The relative balance of IGF-dependent and IGF-independent actions of IGFBP-6 in vivo together with the related question regarding the roles of IGFBP-6 binding to IGF and non-IGF ligands are keys to understanding the physiological role of this protein.
- Subjects :
- Insulin-Like Growth Factor Binding Protein 6
Kinase
Angiogenesis
medicine.medical_treatment
Cell
Chemotaxis
Cell Biology
Biology
Bioinformatics
Biochemistry
law.invention
Cell biology
Insulin-like growth factor
medicine.anatomical_structure
law
Cancer cell
medicine
Suppressor
Molecular Biology
hormones, hormone substitutes, and hormone antagonists
Research Article
Subjects
Details
- ISSN :
- 1873961X and 18739601
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Journal of Cell Communication and Signaling
- Accession number :
- edsair.doi.dedup.....45f7fc370bc20f83f567789d077d92bd
- Full Text :
- https://doi.org/10.1007/s12079-015-0288-4