Evidence map›Paper›PMID 31736210›Full record

ArticleAging cell2020

Amelioration of age-related brain function decline by Bruton's tyrosine kinase inhibition.

Akang E Ekpenyong-Akiba, Marta Poblocka, Mohammad Althubiti, Miran Rada, Diana Jurk, Sandra Germano, Gabriella Kocsis-Fodor, Yu Shi, Juan J Canales, Salvador Macip

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.7field-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

13 citing papers in PubMed, 42 citations in OpenAlex.

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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

10 authors at 3 institutions in 4 countries.

Akang E Ekpenyong-AkibaMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Marta PoblockaMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Mohammad AlthubitiMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Miran RadaMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Diana JurkAgeing Research Laboratories, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.
Sandra GermanoMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Gabriella Kocsis-FodorMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Yu ShiMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.
Juan J CanalesDivision of Psychology, School of Medicine, University of Tasmania, Hobart, TAS, Australia.
Salvador MacipMechanisms of Cancer and Aging Laboratory, Department of Molecular and Cell Biology, University of Leicester, Leicester, UK.ORCID 0000-0003-1963-8840
University of Leicester · GBMayo Clinic in Florida · USUniversity of Tasmania · AU

Funding

M.C. Andreu Memorial Fund
6 · The paper itself

Abstract

One of the hallmarks of aging is the progressive accumulation of senescent cells in organisms, which has been proposed to be a contributing factor to age-dependent organ dysfunction. We recently reported that Bruton's tyrosine kinase (BTK) is an upstream component of the p53 responses to DNA damage. BTK binds to and phosphorylates p53 and MDM2, which results in increased p53 activity. Consistent with this, blocking BTK impairs p53-induced senescence. This suggests that sustained BTK inhibition could have an effect on organismal aging by reducing the presence of senescent cells in tissues. Here, we show that ibrutinib, a clinically approved covalent inhibitor of BTK, prolonged the maximum lifespan of a Zmpste24

Indexed as

Agammaglobulinaemia Tyrosine KinaseAgingAnimalsBrainCognitive DysfunctionHumansMiceProtein Kinase InhibitorsAgammaglobulinaemia Tyrosine KinaseBTK protein, humanProtein Kinase InhibitorsBTKcellular senescencehealthspanp53progeria

Identifiers

PMID31736210
PMCPMC6974713
OpenAlexW2987149078

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.