Evidence map›Paper›PMID 32380258›Full record

ReviewBone2020

Wnt signaling in chondroprogenitors during long bone development and growth.

Takeshi Oichi, Satoru Otsuru, Yu Usami, Motomi Enomoto-Iwamoto, Masahiro Iwamoto

Open access · greenAbstract readReview
In one paragraph

Review in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Overexpression ofFrontiers in cell and developmental biology · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors at 2 institutions in 2 countries.

Takeshi OichiDepartment of Orthopaedics, School of Medicine, University of Maryland, Baltimore, MD, USA.
Satoru OtsuruDepartment of Orthopaedics, School of Medicine, University of Maryland, Baltimore, MD, USA.
Yu UsamiDepartment of Oral Pathology, Osaka University Graduate School of Dentistry, Osaka, Japan.
Motomi Enomoto-IwamotoDepartment of Orthopaedics, School of Medicine, University of Maryland, Baltimore, MD, USA.
Masahiro IwamotoDepartment of Orthopaedics, School of Medicine, University of Maryland, Baltimore, MD, USA. Electronic address: masahiro.iwamoto@som.umaryland.edu.
University of Maryland, Baltimore · USThe University of Osaka · JP

Funding

Mechanisms of Synovial Joint FormationR01AR062908 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI ENOMOTO-IWAMOTO, MOTOMI, PACIFICI, MAURIZIO · 2011 to 2020
$4.5M
Regulation of Skeletal Growth by Nuclear Retinoid ReceptorsR01AR056837 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI IWAMOTO, MASAHIRO, PACIFICI, MAURIZIO · 2009 to 2020
$3.4M
Local Control of endochondral ossification by retinoid-loaded nano-particlesR01AR072713 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHORNY, MICHAEL, IWAMOTO, MASAHIRO · 2018 to 2022
$1.8M
NIAMS NIH HHS R01 AR056837NIAMS NIH HHS R01 AR062908NIAMS NIH HHS R01 AR072713
6 · The paper itself

Abstract

Wnt signaling together with other signaling pathways governs cartilage development and the growth plate function during long bone formation and growth. β-catenin-dependent Wnt signaling is a specific lineage determinant of skeletal mesenchymal cells toward chondrogenic or osteogenic direction. Once cartilage forms and the growth plate organize, Wnt signaling continues to regulate proliferation and differentiation of the growth plate chondrocytes. Although chondrocytes in the growth plate have a high capacity to proliferate, new cells must be supplied to the growth plate from chondroprogenitor population. Advances in in vivo cell tracking techniques have demonstrated the importance of Wnt signaling in driving tissue renewal. The Wnt-responsive cells, genetically marked by the Wnt-reporter system, are found as stem cells in various tissues. Similarly, Wnt-responsive cells are found in the periphery of the growth plate and expanded to constitute entire column structure, indicating that Wnt signaling participates in the regulation of chondroprogenitors in the growth plate. This review will discuss advancements in research of progenitors in the growth plate, specifically focusing on Wnt/β-catenin signaling.

Indexed as

Bone DevelopmentChondrogenesisWnt Signaling PathwayAnimalsbeta CateninCell DifferentiationChondrocytesGrowth PlateHumansbeta CateninChondroprogenitorGrowth plateWnt signaling

Identifiers

PMID32380258
PMCPMC7354209
OpenAlexW3022736461

What OpenQuestion holds

Textmetadata
LicenceTDM
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.