Evidence map›Paper›PMID 31636264›Full record

ArticleNature communications2019

Identification and characterization of Cardiac Glycosides as senolytic compounds.

Francisco Triana-Martínez, Pilar Picallos-Rabina, Sabela Da Silva-Álvarez, Federico Pietrocola, Susana Llanos, Verónica Rodilla, Enrica Soprano, Pablo Pedrosa, Alba Ferreirós, Marta Barradas and 17 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 227 papers.

0numbers the graph read from it
0cells of the map it votes in
227citing papers in PubMed
14.1field-weighted citation impact, top 1% 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

227 citing papers in PubMed, 365 citations in OpenAlex.

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  8. Hallmarks of the ageing lung: 10 years later.The European respiratory journal · 2026
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167 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 8 institutions in 1 country.

Francisco Triana-MartínezLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.
Pilar Picallos-RabinaLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0001-5673-5952
Sabela Da Silva-ÁlvarezLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.
Federico PietrocolaInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), 08028, Barcelona, Spain.
Susana LlanosDNA Replication Group, Spanish National Cancer Research Centre (CNIO), 28029, Madrid, Spain.ORCID http://orcid.org/0000-0002-8555-9326
Verónica RodillaPreclinical Research Program, Vall d´Hebron Institute of Oncology (VHIO) and CIBERONC, Barcelona, Spain.ORCID http://orcid.org/0000-0003-0512-4179
Enrica SopranoCentro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS) and Departamento de Física de Partículas, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0001-6786-9729
Pablo PedrosaLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.
Alba FerreirósLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-7003-8683
Marta BarradasMetabolic Syndrome Group, Madrid Institute for Advanced Studies (IMDEA) in Food, CEI UAM+CSIC, Madrid, E28049, Spain.ORCID http://orcid.org/0000-0001-7122-7251
Fernanda Hernández-GonzálezInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), 08028, Barcelona, Spain.
Marta LalindePreclinical Research Program, Vall d´Hebron Institute of Oncology (VHIO) and CIBERONC, Barcelona, Spain.
Neus PratsInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), 08028, Barcelona, Spain.
Cristina BernadóPreclinical Research Program, Vall d´Hebron Institute of Oncology (VHIO) and CIBERONC, Barcelona, Spain.
Patricia GonzálezHistopathology Unit, Spanish National Cancer Research Centre (CNIO), 28029, Madrid, Spain.
María GómezHistopathology Unit, Spanish National Cancer Research Centre (CNIO), 28029, Madrid, Spain.
Maria P IkonomopoulouTranslational Venomics Group, Madrid Institute for Advanced Studies (IMDEA) in Food, CEI UAM+CSIC, Madrid, E28049, Spain.ORCID http://orcid.org/0000-0001-7739-080X
Pablo J Fernández-MarcosMetabolic Syndrome Group, Madrid Institute for Advanced Studies (IMDEA) in Food, CEI UAM+CSIC, Madrid, E28049, Spain.ORCID http://orcid.org/0000-0003-3515-4125
Tomás García-CaballeroDepartamento de Ciencias Morfológicas, Facultad de Medicina. USC. Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.
Pablo Del PinoCentro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS) and Departamento de Física de Partículas, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0003-1318-6839
Joaquín ArribasPreclinical Research Program, Vall d´Hebron Institute of Oncology (VHIO) and CIBERONC, Barcelona, Spain.
Anxo VidalCiCLOn, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CIMUS), Universidade de Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), E15782, Santiago de Compostela, Spain.
Miguel González-BarciaServicio de Farmacia, Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain.
Manuel SerranoInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), 08028, Barcelona, Spain.ORCID http://orcid.org/0000-0001-7177-9312
María I LozaBioFarma, Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), Universidade de Santiago de Compostela, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Eduardo DomínguezBioFarma, Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), Universidade de Santiago de Compostela, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain. eduardo.dominguez@usc.es.ORCID http://orcid.org/0000-0003-3359-5867
Manuel ColladoLaboratory of Stem Cells in Cancer and Aging, Health Research Institute of Santiago de Compostela (IDIS), Xerencia de Xestión Integrada de Santiago (XXIS/SERGAS), E15706, Santiago de Compostela, Spain. manuel.collado.rodriguez@sergas.es.ORCID http://orcid.org/0000-0002-0330-0880
Universidade de Santiago de Compostela · ESInstituto de Investigación Sanitaria de Santiago · ESInstitute for Research in Biomedicine · ESMadrid Institute for Advanced Studies · ESSpanish National Cancer Research Centre · ESVall d'Hebron Institut de Recerca · ESFundación Pública Galega de Medicina Xenómica · ESInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compounds with specific cytotoxic activity in senescent cells, or senolytics, support the causal involvement of senescence in aging and offer therapeutic interventions. Here we report the identification of Cardiac Glycosides (CGs) as a family of compounds with senolytic activity. CGs, by targeting the Na+/K+ATPase pump, cause a disbalanced electrochemical gradient within the cell causing depolarization and acidification. Senescent cells present a slightly depolarized plasma membrane and higher concentrations of H+, making them more susceptible to the action of CGs. These vulnerabilities can be exploited for therapeutic purposes as evidenced by the in vivo eradication of tumors xenografted in mice after treatment with the combination of a senogenic and a senolytic drug. The senolytic effect of CGs is also effective in the elimination of senescence-induced lung fibrosis. This experimental approach allows the identification of compounds with senolytic activity that could potentially be used to develop effective treatments against age-related diseases.

Indexed as

A549 CellsAnimalsAntibiotics, AntineoplasticApoptosisBleomycinBreast NeoplasmsCardiac GlycosidesCell Line, TumorCell MembraneCellular SenescenceChondrocytesDigoxinFemaleFibroblastsHumansHydrogen-Ion ConcentrationAntibiotics, AntineoplasticBleomycinCardiac GlycosidesDigoxinOuabainProscillaridin

Identifiers

PMID31636264
PMCPMC6803708
OpenAlexW2981220896

What OpenQuestion holds

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Registered trials

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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.