Evidence map›Paper›PMID 35250566›Full record

ArticleFrontiers in pharmacology2022

The Mitochondrial Deubiquitinase USP30 Regulates AKT/mTOR Signaling.

Ruohan Zhang, Serra Ozgen, Hongke Luo, Judith Krigman, Yutong Zhao, Gang Xin, Nuo Sun

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Liproxstatin-1 Protects SH-SY5Y Cells by Inhibiting HInternational journal of molecular sciences · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. The roles of ubiquitination in AML.Annals of hematology · 2024
    Review
  8. Astaxanthin Inhibits HMarine drugs · 2024
    Article
  9. A review of deubiquitinases and thier roles in tumorigenesis and development.Frontiers in bioengineering and biotechnology · 2023
    Review
  10. 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

7 authors at 2 institutions in 1 country.

Ruohan ZhangDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Serra OzgenDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Hongke LuoDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Judith KrigmanDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Yutong ZhaoDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Gang XinPelotonia Institute for Immuno-Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, United States.
Nuo SunDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
The Ohio State University Wexner Medical Center · USThe Ohio State University · US

Funding

Interplay between mitophagy and substrate utilization in heart failure progressionR01HL160581 · NHLBI · OHIO STATE UNIVERSITY · PI Nuo Sun · 2022 to 2026
$2.6M
NHLBI NIH HHS R01 HL160581
6 · The paper itself

Abstract

Mitophagy is an intracellular mechanism to maintain mitochondrial health by removing dysfunctional mitochondria. The E3 ligase Parkin ubiquitinates the membrane proteins on targeted mitochondria to initiate mitophagy, whereas USP30 antagonizes Parkin-dependent mitophagy by removing ubiquitin from Parkin substrates. The AKT/mTOR signaling is a master regulator of cell proliferation, differentiation, apoptosis, and autophagy. Although mounting evidence suggests that perturbations in the AKT/mTOR signaling pathway may contribute to mitophagy regulation, the specific mechanisms between Parkin/USP30 and AKT/mTOR signaling have not been elucidated. In this study, we employ a set of genetic reagents to investigate the role of Parkin and USP30 in regulating the AKT/mTOR signaling during mitophagy. We demonstrated that, in the setting of mitochondrial stress, the AKT/mTOR signaling is regulated, at least in part, by the activity of Parkin and USP30. Parkin inhibits AKT/mTOR signaling following an

Indexed as

aktcancerleukemiamitophagymTORparkinUSP30

Identifiers

PMID35250566
PMCPMC8891576
OpenAlexW4225529211

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.