Evidence map›Paper›PMID 26312549›Full record

ArticleAutophagy2016

AUTEN-67, an autophagy-enhancing drug candidate with potent antiaging and neuroprotective effects.

Diána Papp, Tibor Kovács, Viktor Billes, Máté Varga, Anna Tarnóci, László Hackler, László G Puskás, Hanna Liliom, Krisztián Tárnok, Katalin Schlett and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
4.1field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. Autophagy: A Double-Edged Sword in the Aging ofInternational journal of molecular sciences · 2026
    Review
  4. Article
  5. Autophagy: Regulator of cell death.Cell death & disease · 2023
    Review
  6. Toxics · 2023
    Review
  7. Novel therapeutic approaches to target neurodegeneration.British journal of pharmacology · 2023
    Review
  8. Article
  9. Review
  10. The Small-Molecule Enhancers of Autophagy AUTEN-67 and -99 Delay Ageing inInternational journal of molecular sciences · 2023
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

19 authors at 4 institutions in 4 countries.

Diána Pappa Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Tibor Kovácsa Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Viktor Billesa Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Máté Vargab Department of Genetics , Eötvös Loránd University , Budapest , Hungary.
Anna Tarnócia Velgene Biotechnology Research Ltd. , Szeged , Hungary.
László Hacklerc Avidin Ltd. , Szeged , Hungary.
László G Puskásc Avidin Ltd. , Szeged , Hungary.
Hanna Liliome Department of Physiology and Neurobiology , Eötvös Loránd University , Budapest , Hungary.
Krisztián Tárnoke Department of Physiology and Neurobiology , Eötvös Loránd University , Budapest , Hungary.
Katalin Schlette Department of Physiology and Neurobiology , Eötvös Loránd University , Budapest , Hungary.
Adrienn Borsyg Institute of Enzymology, Research Center for Natural Sciences , Budapest , Hungary.
Zsolt Pádára Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Attila L Kovácsh Department of Anatomy , Cell and Developmental Biology, Eötvös Loránd University , Budapest , Hungary.
Krisztina Hegedűsh Department of Anatomy , Cell and Developmental Biology, Eötvös Loránd University , Budapest , Hungary.
Gábor Juhászh Department of Anatomy , Cell and Developmental Biology, Eötvös Loránd University , Budapest , Hungary.
Marcell Komlósa Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Attila Erdősa Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Balázs Gulyási Karolinska Institute , Department of Clinical Neuroscience , Stockholm , Sweden.
Tibor Vellaia Velgene Biotechnology Research Ltd. , Szeged , Hungary.
Eötvös Loránd University · HUInstitute of Genetics · HUInstitute of Molecular Life Sciences · HUNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a major molecular mechanism that eliminates cellular damage in eukaryotic organisms. Basal levels of autophagy are required for maintaining cellular homeostasis and functioning. Defects in the autophagic process are implicated in the development of various age-dependent pathologies including cancer and neurodegenerative diseases, as well as in accelerated aging. Genetic activation of autophagy has been shown to retard the accumulation of damaged cytoplasmic constituents, delay the incidence of age-dependent diseases, and extend life span in genetic models. This implies that autophagy serves as a therapeutic target in treating such pathologies. Although several autophagy-inducing chemical agents have been identified, the majority of them operate upstream of the core autophagic process, thereby exerting undesired side effects. Here, we screened a small-molecule library for specific inhibitors of MTMR14, a myotubularin-related phosphatase antagonizing the formation of autophagic membrane structures, and isolated AUTEN-67 (autophagy enhancer-67) that significantly increases autophagic flux in cell lines and in vivo models. AUTEN-67 promotes longevity and protects neurons from undergoing stress-induced cell death. It also restores nesting behavior in a murine model of Alzheimer disease, without apparent side effects. Thus, AUTEN-67 is a potent drug candidate for treating autophagy-related diseases.

Indexed as

AgingAmyloid beta-Protein PrecursorAnimalsAutophagyBenzenesulfonamidesDrosophila melanogasterFat BodyFemaleHeLa CellsHumansLongevityMaleMiceNaphthoquinonesNesting BehaviorNeuroprotectionAmyloid beta-Protein PrecursorBenzenesulfonamidesMTMR14 protein, humanN-(3-(benzimidazol-1-yl)-1,4-dioxonaphthalen-2-yl)-4-nitrobenzenesulfonamideNaphthoquinonesNeuroprotective AgentsPhosphoric Monoester HydrolasesSulfonamidesage-dependent diseasesagingAUTEN-67autophagy inductiondrug candidateEDTPHeLa cellsLC3B-IImodel organismMTMR14/JumpyneuroprotectionSQSTM1/p62

Identifiers

PMID26312549
PMCPMC4835959
OpenAlexW2249259354

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.