Evidence map›Paper›PMID 41831318›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Integrative Approaches to Treating Cellular Senescence in Kidney Disease.

Tomoka Misawa, Amruta A, LaTonya J Hickson, Joy Wolfram

Abstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Tomoka MisawaSchool of Chemical Engineering, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0009-0009-9619-3188
Amruta ASchool of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore.ORCID https://orcid.org/0000-0001-6834-0608
LaTonya J HicksonDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, Florida, USA.ORCID https://orcid.org/0000-0002-7485-336X
Joy WolframSchool of Chemical Engineering, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0003-0579-9897

Funding

National Institutes of Health, United States under Award No. R01AG076537
6 · The paper itself

Abstract

Cellular senescence in the kidney plays a crucial role in the progression of acute kidney injury and chronic kidney disease. Therapeutic approaches targeting senescent cells, such as small molecule senolytic and senomorphic drugs, display efficacy in preclinical models. However, such drugs pose a risk of adverse effects and only partially mitigate disease progression, highlighting the need for new therapeutic approaches that more comprehensively and safely address disease pathways in aging kidney disease. This review discusses the potential of extracellular vesicles and longevity proteins, such as α-klotho and silencing information regulator 2-related enzyme 1 (SIRT1), in regulating cellular senescence and alleviating kidney fibrosis. Particularly, combination therapy that simultaneously targets inflammation, tissue damage, and senescence is promising for kidney disease, given the potential to synergistically overcome the limitations of current unimodular treatment modalities and pave the way for more effective management of kidney disease. This review highlights the mechanisms of cellular senescence in kidney disease, particularly in diabetic kidney disease, the latest knowledge on senotherapy, and the potential and challenges of new therapeutic strategies, including combining extracellular vesicles and longevity proteins.

Indexed as

Cellular SenescenceKidney DiseasesSenotherapeuticsAnimalsExtracellular VesiclesHumansSenotherapeuticscellular senescencecombination therapyextracellular vesiclekidney diseaselongevity proteinmesenchymal stem cell

Identifiers

PMID41831318
PMCPMC13073271

What OpenQuestion holds

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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.