Evidence map›Paper›PMID 31005954›Full record

ArticleAging2019

Cooperative impact of thiazolidinedione and fatty acid synthase on human osteogenesis.

Ching-Yun Chen, Kuo-Yun Tseng, Zhe-Hong Wong, Ya-Ping Chen, Ting-Yu Chen, Hsuan-Ying Chen, Zih-Ying Chen, Feng-Huei Lin, Hung-Ming Wu, Shankung Lin

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

10 authors at 5 institutions in 1 country.

Ching-Yun Chen *Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, Taiwan, Republic of China.
Kuo-Yun Tseng *Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Taiwan, Republic of China.
Zhe-Hong WongDepartment of Orthopedics, National Taiwan University Hospital, Hsin-chu Branch, Taiwan, Republic of China.
Ya-Ping ChenInflammation Research and Drug Development Center, Taiwan, Republic of China.
Ting-Yu ChenInflammation Research and Drug Development Center, Taiwan, Republic of China.
Hsuan-Ying ChenInflammation Research and Drug Development Center, Taiwan, Republic of China.
Zih-Ying ChenInflammation Research and Drug Development Center, Taiwan, Republic of China.
Feng-Huei LinInstitute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, Taiwan, Republic of China.
Hung-Ming WuInflammation Research and Drug Development Center, Taiwan, Republic of China.
Shankung LinInflammation Research and Drug Development Center, Taiwan, Republic of China.
Development Center for Biotechnology · TWNational Health Research Institutes · TWChanghua Christian Hospital · TWChina Medical University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous, we found that the small molecules capable of inhibiting the expression and the pro-adipogenic activity of ZNF521 might improve the osteogenic performance of aging human bone marrow MSCs (bmMSCs), and that fatty acid synthase (FASN) was a critical effector of ZNF521's pro-adipogenic activity. Here, by characterizing the netoglitazone (MCC-555), one of the thiazolidinediones known as adipogenic enhancers, as an inhibitor of ZNF521 expression, we found that MCC-555 indeed also harbored pro-osteoblastic effect. Investigation revealed that MCC-555 might function as a GSK3β inhibitor to promote osteoblastogenesis and bone formation. Importantly, combination of MCC-555 with FASN knockdown, but not with GW9662 (a PPARγ2 antagonist), blocked the pro-adipogenic but retained the pro-osteoblastic effect of MCC-555. Using a 3-dimentional culture system, we showed that MCC-555 facilitated the FASN-knockdown of aging human bmMSCs to form cell clusters in scaffolds, and to promote osteoblastic differentiation and biomineralization in cell clusters. These data indicated that MCC-555 promoted bmMSCs to produce bone-like tissues. Our data narrate a thiazolidinedione-based novel strategy to improve the osteogenic performance of aging bmMSCs to support the application of autologous aging bmMSCs in cell therapy and in producing bone-like tissues for repairing bone injury in the elderly.

Indexed as

AdipocytesAdipogenesisBone Marrow CellsCell LineDNA-Binding ProteinsFatty Acid SynthasesGene Knockdown TechniquesHumansMaleMesenchymal Stem CellsMiddle AgedOsteoblastsOsteogenesisThiazolidinedionesDNA-Binding ProteinsFatty Acid SynthasesnetoglitazoneThiazolidinedioneszinc finger protein 521, human3-dimentional cultureautologous cell therapybioreactorbone-like tissuesthiazolidinedione

Identifiers

PMID31005954
PMCPMC6519991
OpenAlexW2936157489

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.