Evidence map›Paper›PMID 30473539›Full record

ArticleBioscience reports2019

TIMP-1 inhibits proliferation and osteogenic differentiation of hBMSCs through Wnt/β-catenin signaling.

Tangzhao Liang, Wenling Gao, Lei Zhu, Jianhua Ren, Hui Yao, Kun Wang, Dehai Shi

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. 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
1.0field-weighted citation impact, top 29% 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, 28 citations in OpenAlex.

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  7. Loss of Parathyroid Hormone Receptor Signaling in Osteoprogenitors Is Associated With Accumulation of Multiple Hematopoietic Lineages in the Bone Marrow.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
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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

7 authors at 1 institution in 1 country.

Tangzhao LiangDepartment of Orthopaedic Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China.
Wenling GaoDepartment of Orthodontics, Hospital of Stomatology, Sun Yat-sen University, No. 56, Lingyuan West Road, 510060 Guangzhou, China.
Lei ZhuDepartment of Plastic and Reconstructive Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China.
Jianhua RenDepartment of Orthopaedic Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China.
Hui YaoDepartment of Orthopaedic Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China.
Kun WangDepartment of Orthopaedic Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China.
Dehai ShiDepartment of Orthopaedic Surgery, the Third Affiliated Hospital of Sun Yat-sen University, No. 600, Tianhe Road, 510630 Guangzhou, China shidehai137@163.com.ORCID 0000-0001-7361-5450
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to evaluate the effect of tissue inhibitor of metalloproteinase-1 (TIMP-1) on the proliferation and osteogenic differentiation potential of human bone marrow-derived MSCs (hBMSCs). hBMSCs with stable TIMP-1 overexpression or TIMP-1 knockdown were generated. Osteogenic differentiation was assessed by Alizarin Red S staining, alkaline phosphatase (ALP) activity and expression of specific markers. Compared with the vehicle controls, TIMP-1 knockdown significantly promoted the growth of hBMSCs. TIMP-1 knockdown up-regulated β-catenin and cyclin D1 proteins. During osteogenic differentiation, TIMP-1 knockdown elevated the deposition of calcium nodules, ALP activity and the mRNA levels of the osteogenic markers sex determining region Y-box 9 (Sox9), CCAAT-enhancer-binding protein and peroxisome proliferator-activated receptor γ. During osteogenic differentiation, TIMP-1 knockdown significantly enhanced the up-regulation of osteocalcin proteins. Meanwhile, TIMP-1 overexpression attenuated the Wnt/activator Wnt3a-induced up-regulation cyclin D1 and Runt-related transcription factor 2 (RUNX-2) (during osteogenic differentiation) proteins, while TIMP-1 knockdown restored the inhibitor Dickkopf 1-induced inhibition effect on the expression of β-catenin, cyclin D1 and RUNX-2. TIMP-1 plays a negative regulatory role in the proliferation and osteogenesis of hBMSCs, at least partially, through Wnt/β-catenin signaling.

Indexed as

beta CateninBiomarkersBone MarrowCell DifferentiationCell ProliferationCore Binding Factor Alpha 1 SubunitHumansMesenchymal Stem CellsOsteocalcinOsteogenesisRNA, MessengerTissue Inhibitor of Metalloproteinase-1Up-RegulationWnt Signaling Pathwaybeta CateninBiomarkersCore Binding Factor Alpha 1 SubunitCTNNB1 protein, humanOsteocalcinRNA, MessengerTIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1Cell proliferationMesenchymal stem cellsOsteogenic differentiationTissue inhibitor of metalloproteinase-1Wnt/β-catenin signaling

Identifiers

PMID30473539
PMCPMC6328886
OpenAlexW2902324753

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.