Evidence map›Paper›PMID 27777301›Full record

ArticleThe Journal of biological chemistry2016

Forkhead Transcription Factor 3a (FOXO3a) Modulates Hypoxia Signaling via Up-regulation of the von Hippel-Lindau Gene (VHL).

Xing Liu, Xiaolian Cai, Bo Hu, Zhichao Mei, Dawei Zhang, Gang Ouyang, Jing Wang, Wei Zhang, Wuhan Xiao

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Deletion of theInternational journal of molecular sciences · 2023
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  14. Hypoxia induces the dormant state in oocytes through expression ofProceedings of the National Academy of Sciences of the United States of America · 2019
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  15. Review
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  17. Article
  18. Deletion of theThe Journal of biological chemistry · 2018
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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

9 authors at 1 institution in 1 country.

Xing LiuFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Xiaolian CaiFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Bo HuFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Zhichao MeiFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Dawei ZhangFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Gang OuyangFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Jing WangFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Wei ZhangFrom the Key Laboratory of Aquatic Biodiversity and Conservation and.
Wuhan XiaoFrom the Key Laboratory of Aquatic Biodiversity and Conservation and w-xiao@ihb.ac.cn.
Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FOXO3a, a member of the forkhead homeobox type O (FOXO) family of transcriptional factors, regulates cell survival in response to DNA damage, caloric restriction, and oxidative stress. The von Hippel-Lindau (VHL) tumor suppressor gene encodes a component of the E3 ubiquitin ligase complex that mediates hypoxia-inducible factor α degradation under aerobic conditions, thus acting as one of the key regulators of hypoxia signaling. However, whether FOXO3a impacts cellular hypoxia stress remains unknown. Here we show that FOXO3a directly binds to the VHL promoter and up-regulates VHL expression. Using a zebrafish model, we confirmed the up-regulation of vhl by foxo3b, an ortholog of mammalian FOXO3a Furthermore, by employing the clustered regularly interspaced short palindromic repeats (CRISPR)-associated RNA-guided endonuclease Cas9 (CRISPR/Cas9) technology, we deleted foxo3b in zebrafish and determined that expression of hypoxia-inducible genes was affected under hypoxia. Moreover, foxo3b-null zebrafish exhibited impaired acute hypoxic tolerance, resulting in death. In conclusion, our findings suggest that, by modulating hypoxia-inducible factor activity via up-regulation of VHL, FOXO3a (foxo3b) plays an important role in survival in response to hypoxic stress.

Indexed as

Response ElementsSignal TransductionUp-RegulationAnimalsCell HypoxiaForkhead Box Protein O3HEK293 CellsHumansTumor Suppressor ProteinsVon Hippel-Lindau Tumor Suppressor ProteinZebrafishZebrafish ProteinsForkhead Box Protein O3FOXO3 protein, humanTumor Suppressor ProteinsVHL protein, humanVhl protein, zebrafishVon Hippel-Lindau Tumor Suppressor ProteinZebrafish ProteinsFOXOhypoxiahypoxia-inducible factor (HIF)pVHLstresstranscription regulationzebrafish

Identifiers

PMID27777301
PMCPMC5207265
OpenAlexW2538350682

What OpenQuestion holds

Textmetadata
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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.