Evidence map›Paper›PMID 35234166›Full record

ArticleJournal of musculoskeletal & neuronal interactions2022

Dok5 regulates proliferation and differentiation of osteoblast via canonical Wnt/β-catenin signaling.

Liang Xu, Junguo Wu, Yueming Yu, Haoran Li, Shiwei Sun, Tieqi Zhang, Minghai Wang

Open access · greenAbstract read
In one paragraph

Article in Journal of musculoskeletal & neuronal interactions, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
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.

Liang Xu *Department of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Junguo Wu *Department of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Yueming YuDepartment of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Haoran LiDepartment of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Shiwei SunDepartment of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Tieqi ZhangDepartment of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Minghai WangDepartment of Orthopedics, The Fifth People's Hospital of Shanghai, Fudan University, China.
Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn bone tissue engineering, the use of osteoblastic seed cells has been widely adopted to mediate the osteogenic differentiation so as to prompt bone regeneration and repair. It is hypothesized that Dok5 can regulate the proliferation and differentiation of osteoblasts. In this study, the role of Dok5 in osteoblast proliferation and differentiation was investigated.

methodsA lentiviral vector to silence Dok5 was transferred to C3H10, 293T and C2C12 cells. CCK-8 assay was used to detect the cell proliferation. Cells were stained by ALP and AR-S staining. Western blot and RT-PCR were used to detect the expression levels of related factors.

resultsDok5 expression level was gradually up-regulated during the osteoblast differentiation. Dok5 silencing down-regulated the expression levels of osteogenic biosignatures OPN, OCN, and Runx2 and suppressed the osteogenesis. Additionally, the osteoblast proliferation and canonical Wnt/β-catenin signaling were suppressed upon Dok5 knockdown, β-catenin expression level was significantly down-regulated in the knockdown group, while the expression levels of GSK3-β and Axin, negative regulators in the Wnt signaling pathway, were up-regulated. Furthermore, overexpression of Dok5 promoted the proliferation and osteogenesis and activated the canonical Wnt/β-catenin signaling pathway.

conclusionDok5 may regulate the osteogenic proliferation and differentiation via the canonical Wnt/β-catenin signaling pathway.

Indexed as

Adaptor Proteins, Signal TransducingOsteogenesisWnt Signaling PathwayAnimalsbeta CateninCell DifferentiationCell ProliferationCells, CulturedGlycogen Synthase Kinase 3HEK293 CellsHumansMiceOsteoblastsAdaptor Proteins, Signal Transducingbeta CateninDOK5 protein, humanDok5 protein, mouseGlycogen Synthase Kinase 3Dok5OsteogenesisProliferationWnt/β-catenin

Identifiers

PMID35234166
PMCPMC8919664
OpenAlexW4214953396

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.