Evidence map›Paper›PMID 31114793›Full record

ArticleMicrobial cell (Graz, Austria)2019

Targeting GATA transcription factors - a novel strategy for anti-aging interventions?

Andreas Zimmermann, Katharina Kainz, Sebastian J Hofer, Maria A Bauer, Sabrina Schroeder, Jörn Dengjel, Federico Pietrocola, Oliver Kepp, Christoph Ruckenstuhl, Tobias Eisenberg and 4 more

Open access · goldAbstract readComment
In one paragraph

Article in Microbial cell (Graz, Austria), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 7 countries.

Andreas ZimmermannInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Katharina KainzInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Sebastian J HoferInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Maria A BauerInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Sabrina SchroederInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Jörn DengjelDepartment of Biology, Université de Fribourg, Switzerland.
Federico PietrocolaInstitute for Research in Biomedicine; Barcelona, Spain.
Oliver KeppEquipe 11 labellisée Ligue contre le Cancer, Centre de Recherche des Cordeliers, INSERM U 1138, Paris, France.
Christoph RuckenstuhlInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Tobias EisenbergInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Stephan J SigristInstitute for Biology/Genetics, Freie Universität Berlin, Berlin, Germany.
Frank MadeoInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
Guido KroemerEquipe 11 labellisée Ligue contre le Cancer, Centre de Recherche des Cordeliers, INSERM U 1138, Paris, France.
Didac Carmona-GutierrezInstitute of Molecular Biosciences, NAWI Graz, University of Graz, Graz, Austria.
University of Graz · ATFreie Universität Berlin · DEInserm · FRInstitute for Research in Biomedicine · ESKarolinska University Hospital · SEUniversity of Fribourg · CH

Funding

Austrian Science Fund FWF W 1226
6 · The paper itself

Abstract

GATA transcription factors (TFs) are a conserved family of zinc-finger TFs that fulfill diverse functions across eukaryotes. Accumulating evidence suggests that GATA TFs also play a role in lifespan regulation. In a recent study, we have identified a natural compound, 4,4' dimethoxychalcone (DMC) that extends lifespan depending on reduced activity of distinct GATA TFs. Prolonged lifespan by DMC treatment depends on autophagy, a protective cellular self-cleaning mechanism. In yeast, DMC reduces the activity of the GATA TF Gln3 and, at the same time, deletion of GLN3 increases autophagy levels during cellular aging per se. Here, we examine current data on the involvement of GATA TFs in the regulation of both autophagy and lifespan in different organisms and explore, if GATA TFs are suitable targets for anti-aging interventions.

Identifiers

PMID31114793
PMCPMC6506692
OpenAlexW2942689714

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.