Evidence map›Paper›PMID 35777359›Full record

ArticleStem cell reports2022

The role of CDK8 in mesenchymal stem cells in controlling osteoclastogenesis and bone homeostasis.

Takanori Yamada, Kazuya Fukasawa, Tetsuhiro Horie, Takuya Kadota, Jiajun Lyu, Kazuya Tokumura, Shinsuke Ochiai, Sayuki Iwahashi, Akane Suzuki, Gyujin Park and 8 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. let-7c-5p promotes fracture healing by downregulating CDK8.Journal of orthopaedic surgery and research · 2026
    Article
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  16. Genetically Engineered Mice Unveil In Vivo Roles of the Mediator Complex.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Review
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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

18 authors at 3 institutions in 1 country.

Takanori YamadaDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Kazuya FukasawaDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Tetsuhiro HorieDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Takuya KadotaDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan; Drug Discovery Research Department, Kyoto Pharmaceutical Industries, Kyoto, Japan.
Jiajun LyuDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Kazuya TokumuraDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Shinsuke OchiaiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Sayuki IwahashiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Akane SuzukiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Gyujin ParkDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Rie UedaDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Megumi YamamotoDrug Discovery Research Department, Kyoto Pharmaceutical Industries, Kyoto, Japan.
Tatsuya KitaoDrug Discovery Research Department, Kyoto Pharmaceutical Industries, Kyoto, Japan.
Hiroaki ShirahaseDrug Discovery Research Department, Kyoto Pharmaceutical Industries, Kyoto, Japan.
Hiroki OchiDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8510, Japan.
Shingo SatoCenter for Innovative Cancer Treatment, Tokyo Medical and Dental University, Tokyo 113-8519, Japan.
Takashi IezakiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan.
Eiichi HinoiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu 501-1196, Japan; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, Gifu 501-1196, Japan. Electronic address: hinoi-e@gifu-pu.ac.jp.
Gifu Pharmaceutical University · JPKyoto Pharmaceutical Industries (Japan) · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone marrow mesenchymal stem cells (MSCs) are critical regulators of postnatal bone homeostasis. Osteoporosis is characterized by bone volume and strength deterioration, partly due to MSC dysfunction. Cyclin-dependent kinase 8 (CDK8) belongs to the transcription-related CDK family. Here, CDK8 in MSCs was identified as important for bone homeostasis. CDK8 level was increased in aged MSCs along with the association with aging-related signals. Mouse genetic studies revealed that CDK8 in MSCs plays a crucial role in bone resorption and homeostasis. Mechanistically, CDK8 in MSCs extrinsically controls osteoclastogenesis through the signal transducer and transcription 1 (STAT1)-receptor activator of the nuclear factor κ Β ligand (RANKL) axis. Moreover, aged MSCs have high osteoclastogenesis-supporting activity, partly through a CDK8-dependent manner. Finally, pharmacological inhibition of CDK8 effectively repressed MSC-dependent osteoclastogenesis and prevented ovariectomy-induced osteoclastic activation and bone loss. These findings highlight that the CDK8-STAT1-RANKL axis in MSCs could play a crucial role in bone resorption and homeostasis.

Indexed as

Bone ResorptionMesenchymal Stem CellsAnimalsCell DifferentiationCyclin-Dependent Kinase 8FemaleHomeostasisMiceNF-kappa BOsteoclastsOsteogenesisRANK LigandCdk8 protein, mouseCyclin-Dependent Kinase 8NF-kappa BRANK LigandCDK8mesenchymal stem cellsosteoporosisRANKL

Identifiers

PMID35777359
PMCPMC9287674
OpenAlexW4283716346

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.