Evidence map›Paper›PMID 35727484›Full record

ReviewJournal of physiology and biochemistry2022

Role of MST1 in the regulation of autophagy and mitophagy: implications for aging-related diseases.

Huayu Shang, Trisha A VanDusseldorp, Ranggui Ma, Yan Zhao, Jason Cholewa, Nelo Eidy Zanchi, Zhi Xia

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of physiology and biochemistry, 2022. 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
2.2field-weighted citation impact, top 12% 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, 14 citations in OpenAlex.

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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

7 authors at 5 institutions in 3 countries.

Huayu Shang *School of Sports Medicine and Health, Chengdu Sport University, Chengdu, China.
Trisha A VanDusseldorp *Department of Exercise Science and Sport Management, Kennesaw State University, Kennesaw, GA, USA.
Ranggui Ma *School of Sports Medicine and Health, Chengdu Sport University, Chengdu, China.
Yan Zhao *Exercise Physiology and Biochemistry Laboratory, College of Physical Education and Health, Wenzhou University, Wenzhou, China.
Jason CholewaDepartment of Exercise Physiology, University of Lynchburg, Lynchburg, VA, USA.
Nelo Eidy ZanchiDepartment of Physical Education, Federal University of Maranhão (UFMA), Sao Luis, MA, Brazil.
Zhi XiaExercise Physiology and Biochemistry Laboratory, College of Physical Education and Health, Wenzhou University, Wenzhou, China. zhixia.ep@hotmail.com.ORCID http://orcid.org/0000-0002-5596-8137
Chengdu Sport University · CNWenzhou University · CNKennesaw State University · USUniversity of Lynchburg · USVale (Brazil) · BR

Funding

Innovative Project of Institute of Sports Medicine and Health of Chengdu Sport University CX21A01Jiangxi Provincial Natural Science Foundation 20192BAB205081Jiangxi Provincial Science Fund for Distinguished Young Scholars 20202ACBL216004National Natural Science Foundation of China 31900842National Natural Science Foundation of China 31960192
6 · The paper itself

Abstract

As a key mechanism to maintain cellular homeostasis under stress conditions, autophagy/mitophagy is related to the occurrence of metabolic disorders, neurodegenerative diseases, cancer, and other aging-related diseases, but the relevant signal pathways regulating autophagy have not been clarified. Mammalian sterile 20-like kinase 1 (MST1) is a central regulatory protein of many metabolic pathways involved in the pathophysiological processes of aging and aging-related diseases and has become a critical integrator affecting autophagic signaling. Recent studies show that MST1 not only suppresses autophagy through directly phosphorylating Beclin-1 and/or inhibiting the protein expression of silent information regulator 1 (SIRT1) in the cytoplasm, but also inhibits BCL2/adenovirus E1B protein-interacting protein 3 (BNIP3)-, FUN14 domain containing 1 (FUNDC1)-, and Parkin (Parkinson protein 2)-mediated mitophagy by interacting with factors such as Ras association domain family 1A (RASSF1A). Indeed, a common pharmacological strategy for anti-aging is to induce autophagy/mitophagy through MST1 inhibition. This article reviews the role and mechanism of MST1 in regulating autophagy during aging, to provide evidence for the development of drugs targeting MST1.

Indexed as

MitochondriaMitophagyAnimalsAutophagyBeclin-1MammalsBeclin-1AgingAging-related diseasesAutophagyMammalian sterile 20-like kinase 1Mitophagy

Identifiers

PMID35727484
OpenAlexW4283267983

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.