Evidence map›Paper›PMID 30012580›Full record

ArticleEMBO molecular medicine2018

A versatile drug delivery system targeting senescent cells.

Daniel Muñoz-Espín, Miguel Rovira, Irene Galiana, Cristina Giménez, Beatriz Lozano-Torres, Marta Paez-Ribes, Susana Llanos, Selim Chaib, Maribel Muñoz-Martín, Alvaro C Ucero and 9 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
15.2field-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

177 citing papers in PubMed, 308 citations in OpenAlex.

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  19. Decoding Vascular Senescence: Cellular Insights and Therapeutic Strategies.International journal of biological sciences · 2026
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117 more citing papers are in PubMed but not listed here.

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 5 institutions in 3 countries.

Daniel Muñoz-EspínTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain dm742@cam.ac.uk manuel.serrano@irbbarcelona.org.ORCID 0000-0002-0550-9514
Miguel RoviraTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID 0000-0002-1391-8465
Irene GalianaInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
Cristina GiménezInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
Beatriz Lozano-TorresInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
Marta Paez-RibesCRUK Cambridge Centre Early Detection Programme, Department of Oncology, Hutchison/MRC Research Centre, University of Cambridge, Cambridge, UK.
Susana LlanosTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Selim ChaibTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Maribel Muñoz-MartínTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Alvaro C UceroGenes, Development and Disease Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Guillermo GarauletMolecular Imaging Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Francisca MuleroMolecular Imaging Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Stephen G DannOncology R&D Group, Pfizer Worldwide Research & Development, Pfizer Inc., La Jolla, CA, USA.
Todd VanArsdaleOncology R&D Group, Pfizer Worldwide Research & Development, Pfizer Inc., La Jolla, CA, USA.
David J ShieldsOncology R&D Group, Pfizer Worldwide Research & Development, Pfizer Inc., La Jolla, CA, USA.
Andrea BernardosInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
José Ramón MurguíaInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
Ramón Martínez-MáñezInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Valencia, Spain.
Manuel SerranoTumor Suppression Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain dm742@cam.ac.uk manuel.serrano@irbbarcelona.org.ORCID 0000-0001-7177-9312
Spanish National Cancer Research Centre · ESUniversitat de València · ESPfizer (United States) · USUniversity of Cambridge · GBInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

Cancer Research UK C9685/A25177Cancer Research UK RG86786Medical Research Council MR/R000530/1
6 · The paper itself

Abstract

Senescent cells accumulate in multiple aging-associated diseases, and eliminating these cells has recently emerged as a promising therapeutic approach. Here, we take advantage of the high lysosomal β-galactosidase activity of senescent cells to design a drug delivery system based on the encapsulation of drugs with galacto-oligosaccharides. We show that gal-encapsulated fluorophores are preferentially released within senescent cells in mice. In a model of chemotherapy-induced senescence, gal-encapsulated cytotoxic drugs target senescent tumor cells and improve tumor xenograft regression in combination with palbociclib. Moreover, in a model of pulmonary fibrosis in mice, gal-encapsulated cytotoxics target senescent cells, reducing collagen deposition and restoring pulmonary function. Finally, gal-encapsulation reduces the toxic side effects of the cytotoxic drugs. Drug delivery into senescent cells opens new diagnostic and therapeutic applications for senescence-associated disorders.

Indexed as

Drug Delivery SystemsAnimalsbeta-GalactosidaseCell SurvivalCellular SenescenceCytotoxinsDisease Models, AnimalDrug CompoundingFluorescent DyesGalactoseHeterograftsLysosomesMiceNeoplasmsNeoplasm TransplantationOligosaccharidesbeta-GalactosidaseCytotoxinsFluorescent DyesGalactoseOligosaccharidespalbociclibPiperazinesPyridineschemotherapyfibrosisnanomedicinepalbociclibsenescence

Identifiers

PMID30012580
PMCPMC6127887
OpenAlexW2884253843

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.