Evidence map›Paper›PMID 26651592›Full record

ReviewTrends in endocrinology and metabolism: TEM2016

Targeting Insulin-Degrading Enzyme to Treat Type 2 Diabetes Mellitus.

Wei-Jen Tang

Open access · greenAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
6.0field-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

65 citing papers in PubMed, 123 citations in OpenAlex.

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  13. Highly toxic Aβ begets more Aβ.Neural regeneration research · 2024
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5 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

1 author at 1 institution in 1 country.

Wei-Jen TangBen-May Department for Cancer Research, the University of Chicago, Chicago, IL, USA. Electronic address: wtang@uchicago.edu.
University of Chicago · US

Funding

Regulation and Catalysis of Human Insulin Degrading EnzymeR01GM081539 · NIGMS · UNIVERSITY OF CHICAGO · PI TANG, WEI-JEN · 2007 to 2015
$2.6M
Image based phenotypic profiling of single-cell responses to perturbationsR01GM081549 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI WU, LANI F · 2007 to 2011
$1.7M
NIGMS NIH HHS R01 GM081539NIGMS NIH HHS R01 GM081549NIGMS NIH HHS R01 GM81549
6 · The paper itself

Abstract

Insulin-degrading enzyme (IDE) selectively degrades peptides, such as insulin, amylin, and amyloid β (Aβ) that form toxic aggregates, to maintain proteostasis. IDE defects are linked to the development of type 2 diabetes mellitus (T2DM) and Alzheimer's disease (AD). Structural and biochemical analyses revealed the molecular basis for IDE-mediated destruction of amyloidogenic peptides and this information has been exploited to develop promising inhibitors of IDE to improve glucose homeostasis. However, the inhibition of IDE can also lead to glucose intolerance. In this review, I focus on recent advances regarding our understanding of the structure and function of IDE and the discovery of IDE inhibitors, as well as challenges in developing IDE-based therapy for human diseases, particularly T2DM.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsDiabetes Mellitus, Type 2Glucose IntoleranceHumansInsulinInsulysinIslet Amyloid PolypeptideAmyloid beta-PeptidesInsulinInsulysinIslet Amyloid PolypeptideAlzheimer's diseaseinsulin degrading enzymesmall molecule inhibitorstype 2 diabetes mellitus

Identifiers

PMID26651592
PMCPMC4698235
OpenAlexW2186890399

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.