Evidence map›Paper›PMID 36875869›Full record

ArticleJournal of osteoporosis2023

The Senolytic Drug Fisetin Attenuates Bone Degeneration in the

William S Hambright, Xiaodong Mu, Xueqin Gao, Ping Guo, Yohei Kawakami, John Mitchell, Michael Mullen, Anna-Laura Nelson, Chelsea Bahney, Haruki Nishimura and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of osteoporosis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  5. Murine Progeria Model Exhibits Delayed Fracture Healing With Senescent Phenotype and Dysregulated Immune Response.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
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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

13 authors at 5 institutions in 2 countries.

William S HambrightSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.ORCID https://orcid.org/0000-0003-4009-8041
Xiaodong MuSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Xueqin GaoSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Ping GuoSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Yohei KawakamiDepartment of Orthopaedic Surgery, Kobe University Graduate School of Medicine, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, JP, Japan.
John MitchellSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Michael MullenSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Anna-Laura NelsonSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Chelsea BahneySteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Haruki NishimuraSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.
Justin HellwinkelDepartment of Orthopedic Surgery, Columbia University, Irving Medical Center, New York Presbyterian Hospital, 622 W 168 St, New York, NY, USA.
Andrew EckDepartment of Orthopaedic Surgery, McGovern Medical School, University of Texas Health Science Center at Houston, 7000 Fannin St, Houston, TX 77030, USA.
Johnny HuardSteadman Philippon Research Institute, Center for Regenerative Sports Medicine, 181 W. Meadow Dr, Vail, CO, USA.ORCID https://orcid.org/0000-0002-2926-569X
Steadman Philippon Research Institute · USKobe University · JPNewYork–Presbyterian Hospital · USThe University of Texas Health Science Center at Houston · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging leads to several geriatric conditions including osteoporosis (OP) and associated frailty syndrome. Treatments for these conditions are limited and none target fundamental drivers of pathology, and thus identifying strategies to delay progressive loss of tissue homeostasis and functional reserve will significantly improve quality of life in elderly individuals. A fundamental property of aging is the accumulation of senescent cells. Senescence is a cell state defined by loss of proliferative capacity, resistance to apoptosis, and the release of a proinflammatory and anti-regenerative senescence-associated secretory phenotype (SASP). The accumulation of senescent cells and SASP factors is thought to significantly contribute to systemic aging. Senolytics-compounds which selectively target and kill senescent cells-have been characterized to target and inhibit anti-apoptotic pathways that are upregulated during senescence, which can elicit apoptosis in senescent cells and relieve SASP production. Senescent cells have been linked to several age-related pathologies including bone density loss and osteoarthritis in mice. Previous studies in murine models of OP have demonstrated that targeting senescent cells pharmacologically with senolytic drugs can reduce symptomology of the disease. Here, we demonstrate the efficacy of senolytic drugs (dasatinib, quercetin, and fisetin) to improve age-associated degeneration in bone using the Zmpste24

Identifiers

PMID36875869
PMCPMC9977556
OpenAlexW4321502148

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.