Evidence map›Paper›PMID 22090472›Full record

ReviewPharmacological reviews2012

Therapeutic implications for striatal-enriched protein tyrosine phosphatase (STEP) in neuropsychiatric disorders.

Susan M Goebel-Goody, Matthew Baum, Constantinos D Paspalas, Stephanie M Fernandez, Niki C Carty, Pradeep Kurup, Paul J Lombroso

Open access · bronzeAbstract readReview
In one paragraph

Review in Pharmacological reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

93 citing papers in PubMed, 158 citations in OpenAlex.

  1. Phosphatase Signaling as a Therapeutic Strategy in Schizophrenia.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Src dependency of the regulation of LTP by alternative splicing ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  6. SHP2 regulates GluA2 tyrosine phosphorylation required for AMPA receptor endocytosis and mGluR-LTD.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Regulation of Phosphorylated State of NMDA Receptor by STEPAntioxidants (Basel, Switzerland) · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Adenosine ATranslational psychiatry · 2021
    Article

33 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 2 countries.

Susan M Goebel-GoodyChild Study Center, Yale University School of Medicine, New Haven, Connecticut, USA.
Matthew Baum
Constantinos D Paspalas
Stephanie M Fernandez
Niki C Carty
Pradeep Kurup
Paul J Lombroso
Wellcome Centre for Ethics and Humanities · GBYale University · USDepartment of Public Health · USUniversity of Oxford · GB

Funding

MOLECULAR AND CELLULAR ANALYSIS OF BRAIN ENRICHED PTPSR01MH052711 · NIMH · YALE UNIVERSITY · PI LOMBROSO, PAUL J · 1999 to 2014
$5.0M
The Role of STEP in SchizophreniaR01MH091037 · NIMH · YALE UNIVERSITY · PI LOMBROSO, PAUL J · 2011 to 2015
$1.8M
MOLECULAR AND CELLULAR ANALYSES OF BRAIN ENRICHED PTPSR29MH052711 · NIMH · YALE UNIVERSITY · PI LOMBROSO, PAUL J · 1994 to 1998
–
NIMH NIH HHS MH052711NIMH NIH HHS MH091037NIMH NIH HHS R01 MH052711NIMH NIH HHS R01 MH091037
6 · The paper itself

Abstract

Striatal-enriched protein tyrosine phosphatase (STEP) is a brain-specific phosphatase that modulates key signaling molecules involved in synaptic plasticity and neuronal function. Targets include extracellular-regulated kinase 1 and 2 (ERK1/2), stress-activated protein kinase p38 (p38), the Src family tyrosine kinase Fyn, N-methyl-D-aspartate receptors (NMDARs), and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs). STEP-mediated dephosphorylation of ERK1/2, p38, and Fyn leads to inactivation of these enzymes, whereas STEP-mediated dephosphorylation of surface NMDARs and AMPARs promotes their endocytosis. Accordingly, the current model of STEP function posits that it opposes long-term potentiation and promotes long-term depression. Phosphorylation, cleavage, dimerization, ubiquitination, and local translation all converge to maintain an appropriate balance of STEP in the central nervous system. Accumulating evidence over the past decade indicates that STEP dysregulation contributes to the pathophysiology of several neuropsychiatric disorders, including Alzheimer's disease, schizophrenia, fragile X syndrome, epileptogenesis, alcohol-induced memory loss, Huntington's disease, drug abuse, stroke/ischemia, and inflammatory pain. This comprehensive review discusses STEP expression and regulation and highlights how disrupted STEP function contributes to the pathophysiology of diverse neuropsychiatric disorders.

Indexed as

Mental DisordersNervous System DiseasesProtein Tyrosine Phosphatases, Non-ReceptorBrainDimerizationHumansPhosphorylationProtein ConformationSubstrate SpecificityProtein Tyrosine Phosphatases, Non-ReceptorPTPN5 protein, human

Identifiers

PMID22090472
PMCPMC3250079
OpenAlexW2135321046

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.