Evidence map›Paper›PMID 37500648›Full record

ArticleCell death & disease2023

A transient increase of HIF-1α during the G1 phase (G1-HIF) ensures cell survival under nutritional stress.

Ratnal Belapurkar, Maximilian Pfisterer, Jan Dreute, Sebastian Werner, Sven Zukunft, Ingrid Fleming, Michael Kracht, M Lienhard Schmitz

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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  10. Computational analysis of treatment resistant cancer cells.Frontiers in cell and developmental biology · 2025
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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

8 authors at 3 institutions in 1 country.

Ratnal BelapurkarInstitute of Biochemistry, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany.ORCID 0000-0003-3238-5294
Maximilian PfistererInstitute of Biochemistry, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany.
Jan DreuteInstitute of Biochemistry, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany.
Sebastian WernerRudolf Buchheim Institute of Pharmacology, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany.
Sven ZukunftInstitute for Vascular Signalling, Goethe University, Frankfurt am Main, Germany.ORCID 0000-0002-1811-4562
Ingrid FlemingInstitute for Vascular Signalling, Goethe University, Frankfurt am Main, Germany.ORCID 0000-0003-1881-3635
Michael KrachtRudolf Buchheim Institute of Pharmacology, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany.ORCID 0000-0002-8501-043X
M Lienhard SchmitzInstitute of Biochemistry, Justus-Liebig-University, Member of the German Center for Lung Research, Giessen, Germany. lienhard.schmitz@biochemie.med.uni-giessen.de.ORCID 0000-0002-6984-7192
German Center for Lung Research · DEGoethe University Frankfurt · DEJustus-Liebig-Universität Gießen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The family of hypoxia-inducible transcription factors (HIF) is activated to adapt cells to low oxygen conditions, but is also known to regulate some biological processes under normoxic conditions. Here we show that HIF-1α protein levels transiently increase during the G1 phase of the cell cycle (designated as G1-HIF) in an AMP-activated protein kinase (AMPK)-dependent manner. The transient elimination of G1-HIF by a degron system revealed its contribution to cell survival under unfavorable metabolic conditions. Indeed, G1-HIF plays a key role in the cell cycle-dependent expression of genes encoding metabolic regulators and the maintenance of mTOR activity under conditions of nutrient deprivation. Accordingly, transient elimination of G1-HIF led to a significant reduction in the concentration of key proteinogenic amino acids and carbohydrates. These data indicate that G1-HIF acts as a cell cycle-dependent surveillance factor that prevents the onset of starvation-induced apoptosis.

Indexed as

ApoptosisHypoxia-Inducible Factor 1, alpha SubunitCell CycleCell HypoxiaCell SurvivalG1 PhaseHypoxia-Inducible Factor 1, alpha Subunit

Identifiers

PMID37500648
PMCPMC10374543
OpenAlexW4385297980

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.