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PMID: 15313400 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

The role of Raf kinase inhibitor protein (RKIP) in health and disease.

Biochemical pharmacology ·Vol. 68 ·No. 6 ·2004-09-15 ·Pages 1049-53

Keller ET, Fu Z, Brennan M

Abstract

Raf kinase inhibitor protein (RKIP) is a member of the phosphatidylethanolamine-binding protein (PEBP) family. RKIP plays a pivotal modulatory role in several protein kinase signaling cascades. RKIP binds inhibits Raf-1-mediated phosphorylation of MEK through binding to Raf-1. Protein kinase C (PKC) phosphorylates RKIP, resulting in release of Raf-1 and activation of MEK and ERK. The phosphorylated RKIP binds to and inhibits G-protein-coupled receptor kinase, resulting in sustained G-protein signaling. The regulatory role that RKIP has in cell signaling is reflected in its role in physiology and pathophysiology. RKIP is involved in neural development, cardiac function and spermatogenesis and appears to have serine protease activity. In addition to its roles in physiology, dysregulated RKIP expression has the potential to contribute to pathophysiological processes including Alzheimer's disease and diabetic nephropathy. RKIP has been shown to fit the criteria of being a metastasis suppressor gene, including having decreased expression in prostate cancer metastases and restoring RKIP expression in a prostate cancer cell line diminishes metastasis in a murine model. Clearly, RKIP has multiple molecular and cellular functions. In this review, RKIP's molecular roles in intracellular signaling, its physiological functions and its role in disease are described.

MeSH Terms
Androgen-Binding Protein Carrier Proteins/physiology Humans Neoplasms/metabolism Phosphatidylethanolamine Binding Protein Proto-Oncogene Proteins c-raf/metabolism Signal Transduction/physiology
Chemicals
Androgen-Binding Protein Carrier Proteins PEBP1 protein, human Phosphatidylethanolamine Binding Protein Proto-Oncogene Proteins c-raf
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Keller Evan T
Department of Urology, University of Michigan, Ann Arbor 48109, USA. [email protected]
Fu Zheng
Brennan Meghan
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
2004-09-15
Pages
1049-53
Language
English
Region
England
NLM ID
0101032
Subset
IM
Grants
NCI NIH HHS · R01-CA098513 · United States
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