Evidence map›Paper›PMID 40022244›Full record

ArticleMicrobiome2025

Microbiota-derived urolithin A in monoclonal gammopathies and multiple myeloma therapy.

Alba Rodríguez-García, Raquel Ancos-Pintado, Roberto García-Vicente, Alejandra Ortiz-Ruiz, Andrés Arroyo, Miguel Ángel Navarro, María Luz Morales, Patricia Guevara-Ramirez, Pablo Justo, Nieves López-Muñoz and 9 more

Abstract read
In one paragraph

Article in Microbiome, 2025. 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
–field-weighted citation impact
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.

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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

19 authors.

Alba Rodríguez-GarcíaHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain. albarodriguezgarcia@hotmail.com.
Raquel Ancos-Pintado *Hematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Roberto García-Vicente *Hematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Alejandra Ortiz-RuizHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Andrés ArroyoHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Miguel Ángel NavarroHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
María Luz MoralesHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Patricia Guevara-RamirezHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Pablo JustoHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Nieves López-MuñozHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
José Sánchez-PinaHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Rafael AlonsoHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
María Victoria SelmaLaboratory of Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Murcia, Spain.
María Dolores Frutos-LisónLaboratory of Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Murcia, Spain.
Rocío García-VillalbaLaboratory of Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Murcia, Spain.
Francisco A Tomás-BarberánLaboratory of Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Murcia, Spain.
Rosa AyalaHematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
Joaquín Martínez-López *Hematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain.
María Linares *Hematological Malignancies Clinical Research CRIS Unit H120-CNIO, Department of Hematology, Hospital Universitario 12 de Octubre, imas12, Universidad Complutense de Madrid, Madrid, Spain. mlinares@ucm.es.

Funding

Fundación Científica Asociación Española Contra el Cáncer Accelerator AwardFundación Científica Asociación Española Contra el Cáncer IDEAS20014LINAISCIII/CDTI PMPTA22/00088MCIN/AEI/10.13039/501100011033 PID2021-123056OA-I00Ministry of Science, Innovation and Universities of Spain FPU19/04933
6 · The paper itself

Abstract

backgroundGut microbiota-derived urolithins may influence multiple myeloma (MM) disease progression and treatment. We analyzed urolithins and their associated microbiota in a retrospective cohort of 45 patients with active MM or premalignant disease using mass spectrometry and 16S rRNA gene sequencing.

resultsPatients with detectable levels of urolithin in serum and stool and a higher abundance of urolithin-related microbiota had a better outcome. Analysis of the effects of urolithin A (UroA) treatment ex vivo, in vitro, and in vivo revealed that UroA is cytotoxic against MM cell lines and modulates the cell cycle and mitochondrial activity. Notably, UroA inhibits the proliferation of primary MM cells in vitro and in a xenograft mouse model, improving overall survival. Finally, combination therapy with UroA and bortezomib has a synergistic effect in vitro, even in the presence of bortezomib resistance, and modulates signaling pathways involved in MM development.

conclusionsUroA might be a potential therapeutic agent to halt MM disease progression or to overcome resistance when used in combination. Video Abstract.

Indexed as

CoumarinsGastrointestinal MicrobiomeMultiple MyelomaAgedAnimalsBortezomibCell Line, TumorCell ProliferationFecesFemaleHumansMaleMiceMiddle AgedRetrospective StudiesRNA, Ribosomal, 16S3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-oneBortezomibCoumarinsRNA, Ribosomal, 16SGut microbiotaMetabolitesMultiple myelomaUrolithin

Identifiers

PMID40022244
PMCPMC11869585

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LicenceCC BY-NC-ND
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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.