Evidence map›Paper›PMID 38196311›Full record

ArticleAging cell2024

Rapid and synchronous chemical induction of replicative-like senescence via a small molecule inhibitor.

Spiros Palikyras, Konstantinos Sofiadis, Athanasia Stavropoulou, Adi Danieli-Mackay, Vassiliki Varamogianni-Mamatsi, David Hörl, Simona Nasiscionyte, Yajie Zhu, Ioanna Papadionysiou, Antonis Papadakis and 13 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  5. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
    Review
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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

23 authors at 8 institutions in 3 countries.

Spiros PalikyrasInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Konstantinos SofiadisInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Athanasia StavropoulouInstitute for Bioinnovation, Biomedical Sciences Research Center "Alexander Fleming", Vari, Greece.
Adi Danieli-MackayInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Vassiliki Varamogianni-MamatsiInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
David HörlFaculty of Biology, Ludwig Maximilians University Munich, Munich, Germany.
Simona NasiscionyteFaculty of Biology, Ludwig Maximilians University Munich, Munich, Germany.
Yajie ZhuInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Ioanna PapadionysiouInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Antonis PapadakisCluster of Excellence on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.
Natasa JosipovicInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
Anne ZirkelCenter for Molecular Medicine Cologne, University and University Hospital of Cologne, Cologne, Germany.
Aoife O'ConnellEIRNA Bio (formerly Ribomaps), Cork, Ireland.
Gary LoughranEIRNA Bio (formerly Ribomaps), Cork, Ireland.
James KeaneEIRNA Bio (formerly Ribomaps), Cork, Ireland.
Audrey MichelEIRNA Bio (formerly Ribomaps), Cork, Ireland.
Wolfgang WagnerHelmholtz-Institute for Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.ORCID https://orcid.org/0000-0002-1971-3217
Andreas BeyerCluster of Excellence on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-3891-2123
Hartmann HarzFaculty of Biology, Ludwig Maximilians University Munich, Munich, Germany.
Heinrich LeonhardtFaculty of Biology, Ludwig Maximilians University Munich, Munich, Germany.
Grazvydas LukinaviciusDepartment of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Christoforos NikolaouInstitute for Bioinnovation, Biomedical Sciences Research Center "Alexander Fleming", Vari, Greece.
Argyris PapantonisInstitute of Pathology, University Medical Center Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0001-7551-1073
Universitätsmedizin Göttingen · DECentral Statistics Office · IELudwig-Maximilians-Universität München · DEAlexander Fleming Biomedical Sciences Research Center · GRUniversity of Cologne · DEMax Planck Institute for Multidisciplinary SciencesRWTH Aachen University · DEUniversity Hospital Cologne · DE

Funding

Erasmus+German Research Foundation 109546710German Research Foundation 422389065German Research Foundation 422857584German Research Foundation 426671079German Research Foundation 469281184International Max Planck Research School for Genome ScienceInternational Max Planck Research School for Molecular Biology
6 · The paper itself

Abstract

Cellular senescence is acknowledged as a key contributor to organismal ageing and late-life disease. Though popular, the study of senescence in vitro can be complicated by the prolonged and asynchronous timing of cells committing to it and by its paracrine effects. To address these issues, we repurposed a small molecule inhibitor, inflachromene (ICM), to induce senescence to human primary cells. Within 6 days of treatment with ICM, senescence hallmarks, including the nuclear eviction of HMGB1 and -B2, are uniformly induced across IMR90 cell populations. By generating and comparing various high throughput datasets from ICM-induced and replicative senescence, we uncovered a high similarity of the two states. Notably though, ICM suppresses the pro-inflammatory secretome associated with senescence, thus alleviating most paracrine effects. In summary, ICM rapidly and synchronously induces a senescent-like phenotype thereby allowing the study of its core regulatory program without confounding heterogeneity.

Indexed as

AgingCellular SenescenceHumans3D genome organizationcellular ageingchromatinSASPsenescencesingle cell genomics

Identifiers

PMID38196311
PMCPMC11019153
OpenAlexW4390697805

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.