Evidence map›Paper›PMID 38483756›Full record

ArticleMolecular biology reports2024

ILK inhibition reduces osteophyte formation through suppression of osteogenesis in BMSCs via Akt/GSK-3β/β-catenin pathway.

Zhixiang Huang, Lixin Huang, Jiali Ding, Yukai Huang, Xuechan Huang, Tianwang Li

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 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

6 authors at 3 institutions in 1 country.

Zhixiang Huang *The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0003-0282-8859
Lixin Huang *The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0009-0006-3298-4253
Jiali DingDepartment of Rheumatology and Immunology, Guangdong Second Provincial General Hospital, No. 466, Xingangzhong Road, Guangzhou, 510317, China.ORCID http://orcid.org/0009-0005-2659-0154
Yukai HuangThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0001-8200-8951
Xuechan HuangThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0003-4961-6407
Tianwang LiThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, China. litian-wang@163.com.ORCID http://orcid.org/0000-0001-6438-2691
Guangdong Provincial People's Hospital · CNGuangdong Medical College · CNFujian Medical University · CN

Funding

3D printing Research Project of Guangdong Second Provincial General Hospital 3D-A2021002Basic and Applied Basic Research Foundation of Guangdong Province 2021A1515110993Science and Technology Projects in Guangzhou 202201010772Science and Technology Projects in Guangzhou 2023A03J0259Science and Technology Projects in Guangzhou 2023A03J0260Science Foundation of Guangdong Second Provincial General Hospital TJGC-2021009
6 · The paper itself

Abstract

backgroundOsteophyte development is a common characteristic of inflammatory skeletal diseases. Elevated osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) participates in pathological osteogenesis. Integrin-linked kinase (ILK) positively regulates the osteoblastic differentiation of osteoprogenitors, but whether the ILK blockage prevents osteophytes and its potential mechanism is still unknown. Furthermore, the low-dose tumor necrosis factor-α (TNF-α) promotes osteogenic differentiation, but a lack of study reports on the relationship between this cytokine and ILK. OSU-T315 is a small ILK inhibitor, which was used to determine the effect of ILK inhibition on osteogenesis and osteophyte formation. METHODS AND

resultsThe osteogenesis of BMSCs was evaluated using Alizarin red S staining, alkaline phosphatase, collagen type I alpha 2 chain, and bone gamma-carboxyglutamate protein. The expression and phosphorylation of protein were assessed through western blot. Immunofluorescence was employed to display the distribution of β-catenin. microCT, hematoxylin-eosin, and safranin O/fast green staining were utilized to observe the osteophyte formation in collagen antibody-induced arthritis mice. We found that ILK blockage significantly declined calcium deposition and osteoblastic markers in a dose- and time-dependent manner. Furthermore, it lowered osteogenesis in the TNF-α-induced inflammatory microenvironment by diminishing the effect of ILK and inactivating the Akt/ GSK-3β/ β-catenin pathway. Nuclear β-catenin was descended by OSU-T315 as well. Finally, the ILK suppression restrained osteophyte formation but not inflammation in vivo.

conclusionsILK inhibition lowered osteogenesis in TNF-α-related inflammatory conditions by deactivating the Akt/ GSK-3β/ β-catenin pathway. This may be a potential strategy to alleviate osteophyte development in addition to anti-inflammatory treatment.

Indexed as

Mesenchymal Stem CellsOsteophyteProtein Serine-Threonine KinasesAnimalsbeta CateninCell DifferentiationCells, CulturedGlycogen Synthase Kinase 3 betaMiceOsteogenesisProto-Oncogene Proteins c-aktScaffold Protein ILKTumor Necrosis Factor-alphaWnt Signaling Pathwaybeta CateninGlycogen Synthase Kinase 3 betaProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktScaffold Protein ILKTumor Necrosis Factor-alphaBone marrow mesenchymal stem cellsCollagen antibody-induced arthritisIntegrin-linked kinaseOsteophyteTumor necrosis factor-α

Identifiers

PMID38483756
OpenAlexW4392818282

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Registered trials

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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.