Evidence map›Paper›PMID 35574058›Full record

ArticleBioactive materials2023

Reversing the imbalance in bone homeostasis via sustained release of SIRT-1 agonist to promote bone healing under osteoporotic condition.

Wei Zhang, Xingzhi Zhou, Weiduo Hou, Erman Chen, Chenyi Ye, Mo Chen, Qian Lu, Xiaohua Yu, Weixu Li

Open access · goldAbstract read
In one paragraph

Article in Bioactive materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 60 citations in OpenAlex.

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  19. Metformin and bone metabolism: unraveling their direct and indirect effects.Therapeutic advances in endocrinology and metabolism · 2025
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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

9 authors at 2 institutions in 1 country.

Wei ZhangDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Xingzhi ZhouDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Weiduo HouDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Erman ChenDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Chenyi YeDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Mo ChenDepartment of Rheumatology, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Qian LuResearch Institute of Orthopaedics, Zhejiang University, 310009, Hangzhou, China.
Xiaohua YuDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Weixu LiDepartment of Orthopedics, Second Affiliated Hospital, School of Medicine, Zhejiang University, 310009, Hangzhou, China.
Second Affiliated Hospital of Zhejiang University · CNHuzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The imbalance of bone homeostasis is the root cause of osteoporosis. However current therapeutic approaches mainly focus on either anabolic or catabolic pathways, which often fail to turn the imbalanced bone metabolism around. Herein we reported that a SIRT-1 agonist mediated molecular therapeutic strategy to reverse the imbalance in bone homeostasis by simultaneously regulating osteogenesis and osteoclastogenesis via locally sustained release of SRT2104 from mineral coated acellular matrix microparticles. Immobilization of SRT2104 on mineral coating (MAM/SRT) harnessing their electrostatic interactions resulted in sustained release of SIRT-1 agonist for over 30 days. MAM/SRT not only enhanced osteogenic differentiation and mineralization, but also attenuated the formation and function of excessive osteoclasts via integrating multiple vital upstream signals (β-catenin, FoxOs, Runx2, NFATc1, etc.)

Indexed as

ALP, Alkaline phosphataseBMM, Bone marrow-derived macrophageBMSCs, Bone marrow-derived mesenchymal stem cellsCCK-8, Cell Counting Kit-8FBS, Fetal bovine serumFTIR, Fourier transform infraredIF, Immunofluorescencemicro-CT, Microcomputed tomographyMineral coatingOPN, OsteopontinOsteoblastOsteoclastOsteoporosisOVX, OvariectomyP1NP, Pro-collagen type 1N-terminal peptideRT-qPCR, Quantitative real-time polymerase chain reactionSBF, Simulated body fluidSEM, Scanning electron microscopysiRNA, Small interfering RNASIRT1WB, Western blotXRD, X-ray diffraction

Identifiers

PMID35574058
PMCPMC9079176
OpenAlexW4225266671

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.