Evidence map›Paper›PMID 25263014›Full record

ReviewSeminars in cell & developmental biology2015

Protein-tyrosine phosphatase 1B substrates and metabolic regulation.

Jesse Bakke, Fawaz G Haj

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. A Systematic Review ofMolecules (Basel, Switzerland) · 2022
    Pooled it
  2. Flavonoids fromJournal of enzyme inhibition and medicinal chemistry · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. medRxiv : the preprint server for health sciences · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Protein tyrosine phosphatase 1B is a regulator of alpha-actinin4 in the glomerular podocyte.Biochimica et biophysica acta. Molecular cell research · 2024
    Article
  19. The importance of including the C-terminal domain of PTP1BJournal of enzyme inhibition and medicinal chemistry · 2023
    Article
  20. Review

2 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

2 authors at 1 institution in 1 country.

Jesse BakkeDepartment of Nutrition, University of California Davis, One Shields Ave, Davis, CA 95616, United States.
Fawaz G HajDepartment of Nutrition, University of California Davis, One Shields Ave, Davis, CA 95616, United States; Division of Endocrinology, Diabetes and Metabolism, Department of Internal Medicine, University of California Davis, Sacramento, CA 95817, United States; Comprehensive Cancer Center, University of California Davis, Sacramento, CA 95817, United States. Electronic address: fghaj@ucdavis.edu.
University of California, Davis · US

Funding

Role of adipose protein-tyrosine phosphatase 1B in glucose homeostasis and body mR01DK090492 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAJ, FAWAZ GEORGE · 2011 to 2015
$1.7M
Role of T cell protein-tyrosine phosphatase in pancreatic islet functionR01DK095359 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAJ, FAWAZ GEORGE · 2014 to 2017
$1.4M
Role of Protein-Tyrosine Phosphatase 1B in Pancreatic Islet FunctionR56DK084317 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAJ, FAWAZ GEORGE · 2010 to 2010
$230k
Metabolic functions of adipose pyruvate kinase M2K99DK100736 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BETTAIEB, AHMED · 2013 to 2014
$180k
NIDDK NIH HHS K99 DK100736NIDDK NIH HHS R01 DK090492NIDDK NIH HHS R01 DK095359NIDDK NIH HHS R56 DK084317
6 · The paper itself

Abstract

Metabolic homeostasis requires integration of complex signaling networks which, when deregulated, contribute to metabolic syndrome and related disorders. Protein-tyrosine phosphatase 1B (PTP1B) has emerged as a key regulator of signaling networks that are implicated in metabolic diseases such as obesity and type 2 diabetes. In this review, we examine mechanisms that regulate PTP1B-substrate interaction, enzymatic activity and experimental approaches to identify PTP1B substrates. We then highlight findings that implicate PTP1B in metabolic regulation. In particular, insulin and leptin signaling are discussed as well as recently identified PTP1B substrates that are involved in endoplasmic reticulum stress response, cell-cell communication, energy balance and vesicle trafficking. In summary, PTP1B exhibits exquisite substrate specificity and is an outstanding pharmaceutical target for obesity and type 2 diabetes.

Indexed as

Signal TransductionAnimalsDiabetes Mellitus, Type 2Endoplasmic Reticulum StressHumansLeptinObesityProtein Tyrosine Phosphatase, Non-Receptor Type 1ThermodynamicsLeptinProtein Tyrosine Phosphatase, Non-Receptor Type 1DiabetesER stressObesityPTP1BPyruvate kinaseSubstrate

Identifiers

PMID25263014
PMCPMC4339617
OpenAlexW1975914587

What OpenQuestion holds

Textmetadata
LicenceTDM
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.