Evidence map›Paper›PMID 25944222›Full record

ArticleExpert opinion on therapeutic targets2015

The potential of sestrins as therapeutic targets for diabetes.

Xiaocheng Charlie Dong

Abstract read
In one paragraph

Article in Expert opinion on therapeutic targets, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. The functions and roles of sestrins in regulating human diseases.Cellular & molecular biology letters · 2022
    Review
  8. Article
  9. Sestrin2 and Beclin1 levels in Polycystic Ovary Syndrome.Journal of clinical laboratory analysis · 2021
    Article
  10. Amino Acids in Autophagy: Regulation and Function.Advances in experimental medicine and biology · 2021
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. 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

1 author.

Xiaocheng Charlie DongIndiana University School of Medicine, Department of Biochemistry and Molecular Biology , IN 46202 , USA xcdong@iu.edu.

Funding

Regulation of hepatic lipid metabolism by a novel Foxo pathwayR01DK091592 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI DONG, X. CHARLIE · 2012 to 2016
$1.7M
NIDDK NIH HHS R01DK09159NIDDK NIH HHS R01 DK091592
6 · The paper itself

Abstract

Sestrins (Sesn1/2/3) belong to a small protein family that has versatile biological functions. In addition to initially characterized oxidoreductase activity, sestrins also have oxidoreductase-independent functions, including activation of AMP-activated protein kinase, inhibition of the mechanistic target of rapamycin complex 1 (mTORC1) and activation of mTORC2. As these kinases are important for metabolic regulation, sestrins have a favorable profile as potential therapeutic targets for metabolic diseases such as diabetes. Recent data are in line with such a notion. In this editorial, I have attempted to provide a brief update on the major findings in regard to sestrins in metabolism.

Indexed as

AnimalsDiabetes MellitusHeat-Shock ProteinsHumansMolecular Targeted TherapyNuclear ProteinsSestrinsHeat-Shock ProteinsNuclear ProteinsSESN1 protein, humanSESN2 protein, humanSESN3 protein, humanSestrinsmechanistic target of rapamycin complex 1mechanistic target of rapamycin complex 2sestrinv-akt murine thymoma viral oncogene homolog

Identifiers

PMID25944222
PMCPMC4504765

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.