Evidence map›Paper›PMID 32888126›Full record

ReviewMolecular biology reports2020

Sestrins: Darkhorse in the regulation of mitochondrial health and metabolism.

Ashish Kumar, Deepshikha Dhiman, Chandrima Shaha

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Sestrin2 in diabetes and diabetic complications.Frontiers in endocrinology · 2023
    Review
  8. The functions and roles of sestrins in regulating human diseases.Cellular & molecular biology letters · 2022
    Review
  9. Review
  10. Article
  11. Review
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

3 authors at 3 institutions in 2 countries.

Ashish KumarDepartment of Biotechnology, University of Helsinki, Helsinki, Finland. mito.ashu1@gmail.com.ORCID http://orcid.org/0000-0002-8018-0237
Deepshikha DhimanDr. Yashwant Singh Parmar Govt. Medical College, Nahan, Himachal Pradesh, India.
Chandrima ShahaCell Death and Differentiation Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, India.
Government Medical College · INNational Institute of Immunology · INUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Every disease is an outcome of one or more stress signals which get convened at the interface of the mitochondria. Mitochondria and metabolism are inextricably anchored to each other and a disruption in either can result in the generation of stressors, which can lead to detrimental health consequences. Stowing everything in one frame reflects that the proteins involved in the sensing of stressors are fundamental for the initiation of various pathologies and their detailed study is necessary for proper understanding of disease mechanisms. Sestrins, a class of evolutionarily conserved, stress inducible genes are activated by a wide range of stressors such as oxidative, genotoxic, and metabolic and play a role in cellular homeostasis. In addition, recent reports have highlighted their importance in governing the mitochondrial dynamics and metabolism. However, their spectrum of involvement in various pathologies has not been dissected out very well. This review will focus and discuss the role of Sestrins mainly Sestrin2 and associated nexus in the context of mitochondria, metabolism, and health.

Indexed as

DNA DamageOxidative StressHumansMitochondriaNuclear ProteinsSestrinsNuclear ProteinsSESN2 protein, humanSestrinsHealthMetabolismMitochondriaSestrin2

Identifiers

PMID32888126
OpenAlexW3083716904

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.