Evidence map›Paper›PMID 33706682›Full record

ArticleAutophagy2021

TP53/p53-FBXO22-TFEB controls basal autophagy to govern hormesis.

Narumi Suzuki, Yoshikazu Johmura, Teh-Wei Wang, Toshiro Migita, Wenwen Wu, Rei Noguchi, Kiyoshi Yamaguchi, Yoichi Furukawa, Shuhei Nakamura, Ichiro Miyoshi and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Targeting glutathione metabolism for tumor radiosensitization (Review).International journal of molecular medicine · 2026
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  12. LncRNA XXYLT1-AS2 promotes tumor progression via autophagy inhibition through ubiquitinated degradation of TFEB in hepatocellular carcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  13. Review
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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

13 authors at 4 institutions in 1 country.

Narumi SuzukiDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Yoshikazu JohmuraDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Teh-Wei WangDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Toshiro MigitaDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Wenwen WuDepartment of Translational Oncology, St. Marianna University Graduate School of Medicine, Kawasaki, Japan.
Rei NoguchiDivision of Clinical Genome Research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Kiyoshi YamaguchiDivision of Clinical Genome Research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Yoichi FurukawaDivision of Clinical Genome Research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Shuhei NakamuraDepartment of Genetics, Graduate School of Medicine, Osaka University, Osaka, Japan.
Ichiro MiyoshiDepartment of Laboratory Animal Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tamotsu YoshimoriDepartment of Genetics, Graduate School of Medicine, Osaka University, Osaka, Japan.
Tomohiko OhtaDepartment of Translational Oncology, St. Marianna University Graduate School of Medicine, Kawasaki, Japan.
Makoto NakanishiDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.ORCID 0000-0002-6707-3584
Tokyo University of Science · JPSt. Marianna University School of Medicine · JPThe University of Osaka · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preconditioning with a mild stressor such as fasting is a promising way to reduce severe side effects from subsequent chemo- or radiotherapy. However, the underlying mechanisms have been largely unexplored. Here, we demonstrate that the TP53/p53-FBXO22-TFEB (transcription factor EB) axis plays an essential role in this process through upregulating basal macroautophagy/autophagy. Mild stress-activated TP53 transcriptionally induced FBXO22, which in turn ubiquitinated KDM4B (lysine-specific demethylase 4B) complexed with MYC-NCOR1 suppressors for degradation, leading to transcriptional induction of TFEB. Upregulation of autophagy-related genes by increased TFEB dramatically enhanced autophagic activity and cell survival upon following a severe stressor. Mitogen-induced AKT1 activation counteracted this process through the phosphorylation of KDM4B, which inhibited FBXO22-mediated ubiquitination. Additionally,

Indexed as

AutophagyHormesisAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCells, CulturedF-Box ProteinsFemaleFibroblastsHumansMaleMiceMice, Inbred C57BLMice, KnockoutReceptors, Cytoplasmic and NuclearTumor Suppressor Protein p53UbiquitinationBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsF-Box ProteinsFBXO22 protein, humanReceptors, Cytoplasmic and NuclearTFEB protein, humanTP53 protein, humanTumor Suppressor Protein p53AKT1autophagyFBXO22hormesisKDM4BMYCTP53ubiquitination

Identifiers

PMID33706682
PMCPMC8632335
OpenAlexW3135168286

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.