Evidence map›Paper›PMID 17706925›Full record

ReviewCellular signalling2008

Signaling crossroads: the function of Raf kinase inhibitory protein in cancer, the central nervous system and reproduction.

Jan Klysik, Steven J Theroux, John M Sedivy, Jeffrey S Moffit, Kim Boekelheide

Open access · greenAbstract readReview
In one paragraph

Review in Cellular signalling, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
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  10. Observational
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  15. Expression of RKIP in chronic myelogenous leukemia K562 cell and inhibits cell proliferation by regulating the ERK/MAPK pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  16. Article
  17. Low RKIP expression associates with poor prognosis in bladder cancer patients.Virchows Archiv : an international journal of pathology · 2013
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jan KlysikDepartment of Molecular Biology Cell Biology and Biochemistry, Brown University, Providence, RI 02912, United States. Jan_Klysik@Brown.edu
Steven J Theroux
John M Sedivy
Jeffrey S Moffit
Kim Boekelheide
Brown University · USAssumption College · US

Funding

Vapor Pressures and Thermodynamic Properties of Complex Organic MixturesP42ES013660 · NIEHS · BROWN UNIVERSITY · PI BOEKELHEIDE, KIM, HURT, ROBERT H. · 2005 to 2020
$37.7M
WNT SIGNALING IN HEPATOCELLULAR CARCINOMAP20RR015578 · NCRR · BROWN UNIVERSITY · PI SCHORL, CHRISTOPH · 2000 to 2009
$22.8M
NCRR NIH HHS 5P20RR015578-07NCRR NIH HHS P20 RR015578NIEHS NIH HHS 5P42ES013660-02NIEHS NIH HHS P42 ES013660
6 · The paper itself

Abstract

The Raf kinase inhibitory protein 1 (RKIP-1) and its orthologs are conserved throughout evolution and widely expressed in eukaryotic organisms. In its non-phosphorylated form RKIP-1 negatively regulates the Raf/MEK/ERK pathway by interfering with the activity of Raf-1. In its phosphorylated state, RKIP-1 dissociates from Raf-1 and inhibits GRK-2, a negative regulator of G-protein coupled receptors (GPCRs). Available data indicate that the phosphorylation of RKIP-1 by PKC can stimulate both the Raf/MEK/ERK and GPCR pathways. RKIP-1 has also been implicated as a negative regulator of the NF-kappaB pathway. Recent studies have shown that phosphorylated RKIP-1 binds to the centrosomal and kinetochore regions of metaphase chromosomes, where it may be involved in regulating the partitioning of chromosomes and the progression through mitosis. The collective evidence indicates that RKIP-1 regulates the activity and mediates the crosstalk between several important cellular signaling pathways. A variety of ablative interventions suggest that reduced RKIP-1 function may influence metastasis, angiogenesis, resistance to apoptosis, and genome integrity. Attenuation of RKIP-1 may also affect cardiac and neurological functions, spermatogenesis, sperm decapacitation, and reproductive behavior. In this review, the role of RKIP-1 in cellular signaling, and especially its functions revealed using a mouse knockout model, are discussed.

Indexed as

Alzheimer DiseaseAnimalsCentral Nervous SystemMiceMice, KnockoutNeoplasmsPhosphatidylethanolamine Binding ProteinReproductionSignal TransductionSpermatogenesisPhosphatidylethanolamine Binding Protein

Identifiers

PMID17706925
PMCPMC2231335
OpenAlexW2069350121

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.