Evidence map›Paper›PMID 31345466›Full record

ReviewThe American journal of pathology2019

Notch Signaling in Osteogenesis, Osteoclastogenesis, and Angiogenesis.

Zhengliang Luo, Xifu Shang, Hao Zhang, Guangxi Wang, Patrick A Massey, Shane R Barton, Christopher G Kevil, Yufeng Dong

Open access · bronzeAbstract readReview
In one paragraph

Review in The American journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 156 citations in OpenAlex.

  1. Pooled it
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  13. Brain-Bone Axis in Physiological and Pathological Conditions.International journal of molecular sciences · 2025
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35 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 2 countries.

Zhengliang LuoDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana; Department of Orthopedic Surgery, the First Affiliated Hospital of University of Science and Technology of China, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Xifu ShangDepartment of Orthopedic Surgery, the First Affiliated Hospital of University of Science and Technology of China, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China. Electronic address: shangxifu@163.com.
Hao ZhangDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana.
Guangxi WangDepartment of Orthopedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Patrick A MasseyDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana.
Shane R BartonDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana.
Christopher G KevilDepartment of Pathology, Louisiana State University Health Sciences Center, Shreveport, Louisiana.
Yufeng DongDepartment of Orthopedic Surgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana. Electronic address: ydong@lsuhsc.edu.
Louisiana State University Health Sciences Center Shreveport · USUniversity of Science and Technology of China · CNHarbin Medical University · CN

Funding

Stress Exacerbates Myocardial Ischemic Injury by Blocking Estrogen's Antidoxidant Protection in the Female HeartP20GM121307 · NIGMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI Christopher G Kevil · 2018 to 2026
$23.6M
Notch-enriched Mesenchymal Stromal Cells for Bone Allograft RepairR01AR073277 · NIAMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI DONG, YUFENG · 2019 to 2024
$1.6M
NIAMS NIH HHS R01 AR073277NIGMS NIH HHS P20 GM121307
6 · The paper itself

Abstract

Skeletal tissue development and regeneration in mammals are intricate, multistep, and highly regulated processes. Various signaling pathways have been implicated in the regulation of these processes, including Notch. Notch signaling is a highly conserved, intercellular signaling pathway that regulates cell proliferation and differentiation, determines cell fate decision, and participates in cellular process in embryonic and adult tissue. Here, we review recent data showing the regulation of Notch signaling in osteogenesis, osteoclastogenesis, and angiogenesis. These processes are cell-context-dependent via direct or indirect mechanisms. Furthermore, Notch signaling may be highly beneficial for efficient coupling of osteogenesis and angiogenesis for tissue engineering and skeletal repair, which is critical to develop clinically therapeutic options.

Indexed as

AnimalsCell DifferentiationCell ProliferationHumansNeovascularization, PhysiologicOsteogenesisReceptors, NotchSignal TransductionReceptors, Notch

Identifiers

PMID31345466
PMCPMC6699068
OpenAlexW2962786907

What OpenQuestion holds

Textmetadata
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.