Evidence map›Paper›PMID 18199690›Full record

ReviewEndocrine reviews2008

The role of membrane glycoprotein plasma cell antigen 1/ectonucleotide pyrophosphatase phosphodiesterase 1 in the pathogenesis of insulin resistance and related abnormalities.

Ira D Goldfine, Betty A Maddux, Jack F Youngren, Gerald Reaven, Domenico Accili, Vincenzo Trischitta, Riccardo Vigneri, Lucia Frittitta

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Endocrine reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
5.8field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 137 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
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  11. Review
  12. The purinergic signalling and inflammation in the pathogenesis and progression of diabetes: key factors and therapeutic targets.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  13. Role of GALNT2 on Insulin Sensitivity, Lipid Metabolism and Fat Homeostasis.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. The hepatic ectonucleotide pyrophosphatase/phosphodiesterase 1 gene mRNA abundance is reduced by insulin and induced by dexamethasone.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2018
    Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Ira D GoldfineDepartment of Medicine and Diabetes Center, University of California San Francisco, San Francisco, California 94143, USA. ira.goldfine@ucsf.edu
Betty A Maddux
Jack F Youngren
Gerald Reaven
Domenico Accili
Vincenzo Trischitta
Riccardo Vigneri
Lucia Frittitta
University of California, San Francisco · USColumbia University · USOspedale Garibaldi · ITSapienza University of Rome · ITStanford University · USUniversity of Catania · IT

Funding

PC-1 Insulin Receptor SignalingR01DK056933 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOLDFINE, IRA D. · 2001 to 2009
$2.6M
NIDDK NIH HHS DK-56933NIDDK NIH HHS R01 DK056933
6 · The paper itself

Abstract

Insulin resistance is a major feature of most patients with type 2 diabetes mellitus (T2D). A number of laboratories have observed that PC-1 (membrane [corrected] glycoprotein plasma cell antigen 1; also termed [corrected] ectonucleotide pyrophosphatase phosphodiesterase 1 or ENPP1) [corrected] is either overexpressed or overactive in muscle, adipose tissue, fibroblasts, and other tissues of insulin-resistant individuals, both nondiabetic and diabetic. Moreover, PC-1 (ENPP1) overexpression [corrected] in cultured cells in vitro and in transgenic mice in vivo, [corrected] impairs insulin stimulation of insulin receptor (IR) activation and downstream signaling. PC-1 binds to the connecting domain of the IR alpha-subunit that is located in residues 485-599. The connecting domain transmits insulin binding in the alpha-subunit to activation of tyrosine kinase activation in the beta-subunit. When PC-1 is overexpressed, it inhibits insulin [corrected]induced IR beta-subunit tyrosine kinase activity. In addition, a polymorphism of PC-1 (K121Q) in various ethnic populations is closely associated with insulin resistance, T2D, and cardio [corrected] and nephrovascular diseases. The product of this polymorphism has a 2- to 3-fold increased binding affinity for the IR and is more potent than the wild-type PC-1 protein (K121K) in inhibiting the IR. These data suggest therefore that PC-1 is a candidate protein that may play a role in human insulin resistance and T2D by its overexpression, its overactivity, or both.

Indexed as

Insulin ResistanceAnimalsDiabetes ComplicationsDiabetes Mellitus, Type 2Disease Models, AnimalFemaleGene ExpressionGenetic VariationHumansObesityPhosphoric Diester HydrolasesPolycystic Ovary SyndromePolymorphism, GeneticProtein Structure, QuaternaryPyrophosphatasesReceptor, Insulinectonucleotide pyrophosphatase phosphodiesterase 1Phosphoric Diester HydrolasesPyrophosphatasesReceptor, Insulin

Identifiers

PMID18199690
PMCPMC2244935
OpenAlexW2149167166

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.