Evidence map›Paper›PMID 35091552›Full record

ReviewBone research2022

Protein tyrosine phosphatases in skeletal development and diseases.

Huiliang Yang, Lijun Wang, Christian Shigley, Wentian Yang

Open access · goldAbstract readReview
In one paragraph

Review in Bone research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. SHP2 ablation mitigates osteoarthritic cartilage degeneration by promoting chondrocyte anabolism through SOX9.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. From Stem to Sternum: The Role of Shp2 in the Skeleton.Calcified tissue international · 2023
    Review
  17. Article
  18. Review
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

4 authors at 2 institutions in 2 countries.

Huiliang Yang *Department of Orthopaedic Surgery and Orthopaedic Research Institute, West China Hospital of Sichuan University, Chengdu, 610041, Sichuan, China.
Lijun Wang *Department of Orthopaedic Surgery, Rhode Island Hospital and Brown University Alpert Medical School, Providence, RI, 02903, USA.
Christian ShigleyDepartment of Orthopaedic Surgery, Rhode Island Hospital and Brown University Alpert Medical School, Providence, RI, 02903, USA.
Wentian YangDepartment of Orthopaedic Surgery, Rhode Island Hospital and Brown University Alpert Medical School, Providence, RI, 02903, USA. wentian_yang@brown.edu.ORCID http://orcid.org/0000-0002-2127-6239
Brown University · USSichuan University · CN

Funding

Stem Cells and AgingP20GM119943 · NIGMS · RHODE ISLAND HOSPITAL · PI WEBB, ASHLEY E · 2017 to 2021
$10.6M
Role of PTPN11 in Cartilage Stem Cells and TumorigenesisR01AR066746 · NIAMS · RHODE ISLAND HOSPITAL · PI YANG, WENTIAN · 2015 to 2019
$1.8M
Role of GI OSTERIX in Gut and Bone BiologyR21AR079195 · NIAMS · RHODE ISLAND HOSPITAL · PI YANG, WENTIAN · 2021 to 2021
$394k
Shp2 in Osteoclastogenesis and Bone RemodelingR21AR057156 · NIAMS · RHODE ISLAND HOSPITAL · PI YANG, WENTIAN · 2009 to 2010
$378k
NIAMS NIH HHS R01 AR066746NIAMS NIH HHS R21 AR057156NIAMS NIH HHS R21 AR079195NIGMS NIH HHS P20 GM119943U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R21AR57156U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) RO1AR066746U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) 1P20 GM119943
6 · The paper itself

Abstract

Skeletal development and homeostasis in mammals are modulated by finely coordinated processes of migration, proliferation, differentiation, and death of skeletogenic cells originating from the mesoderm and neural crest. Numerous molecular mechanisms are involved in these regulatory processes, one of which is protein posttranslational modifications, particularly protein tyrosine phosphorylation (PYP). PYP occurs mainly through the action of protein tyrosine kinases (PTKs), modifying protein enzymatic activity, changing its cellular localization, and aiding in the assembly or disassembly of protein signaling complexes. Under physiological conditions, PYP is balanced by the coordinated action of PTKs and protein tyrosine phosphatases (PTPs). Dysregulation of PYP can cause genetic, metabolic, developmental, and oncogenic skeletal diseases. Although PYP is a reversible biochemical process, in contrast to PTKs, little is known about how this equilibrium is modulated by PTPs in the skeletal system. Whole-genome sequencing has revealed a large and diverse superfamily of PTP genes (over 100 members) in humans, which can be further divided into cysteine (Cys)-, aspartic acid (Asp)-, and histidine (His)-based PTPs. Here, we review current knowledge about the functions and regulatory mechanisms of 28 PTPs involved in skeletal development and diseases; 27 of them belong to class I and II Cys-based PTPs, and the other is an Asp-based PTP. Recent progress in analyzing animal models that harbor various mutations in these PTPs and future research directions are also discussed. Our literature review indicates that PTPs are as crucial as PTKs in supporting skeletal development and homeostasis.

Identifiers

PMID35091552
PMCPMC8799702
OpenAlexW4210564509

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.