Evidence map›Paper›PMID 16951988›Full record

ReviewReviews in endocrine & metabolic disorders2006

Molecular regulation of osteoclast activity.

Angela Bruzzaniti, Roland Baron

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Reviews in endocrine & metabolic disorders, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02972138 (Vitamin D Supplementation and Anti-resorptive Therapy), which is not on this map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 6% 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.

NCT02972138 completednot on this mapstarted 2010, after this paper: background citation

Vitamin D Supplementation and Anti-resorptive Therapy (Bisphosphonates) Treatment of Young Adult Patients With Sickle Cell Disease

TypeobservationalSponsorSocietà Italiana Talassemie ed EmoglobinopatieRan2010 to 2017Enrolled80ConditionsSickle Cells Disease
3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 172 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Chordoma cells possess bone-dissolving activity at the bone invasion front.Cellular oncology (Dordrecht, Netherlands) · 2024
    Article
  9. Article
  10. Review
  11. Open Thy Lattice Osteoclast, Resorb me!The Journal of cell biology · 2023
    Article
  12. Review
  13. Article
  14. Pharmaceutics · 2022
    Article
  15. Article
  16. Review
  17. Role of OSCAR Signaling in Osteoclastogenesis and Bone Disease.Frontiers in cell and developmental biology · 2021
    Review
  18. Article
  19. Quantification of Osteoclasts in Culture, Powered by Machine Learning.Frontiers in cell and developmental biology · 2021
    Article
  20. Article

10 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

2 authors at 1 institution in 1 country.

Angela BruzzanitiDepartment of Orthopaedics, Yale University School of Medicine, New Haven, CT 06510, USA. angela.bruzzaniti@yale.edu
Roland Baron
Yale University · US

Funding

ROLE OF THE C-SRC PROTO-ONCOGENE IN OSTEOCLASTSR01AR042927 · NIAMS · YALE UNIVERSITY · PI BARON, ROLAND E · 1994 to 2009
$3.7M
Regulation of Osteoclastic Bone Resorption:Role of Cb1bR01DE004724 · NIDCR · YALE UNIVERSITY · PI BARON, ROLAND E · 1985 to 2008
$2.0M
REGULATION OF OSTEOCLASTIC BONE RESORPTIONR37DE004724 · NIDCR · YALE UNIVERSITY · PI BARON, ROLAND E · 1993 to 2002
$998k
NIAMS NIH HHS AR42927NIDCR NIH HHS DE04724
6 · The paper itself

Abstract

Osteoclasts are multinucleated cells derived from hematopoietic precursors that are primarily responsible for the degradation of mineralized bone during bone development, homeostasis and repair. In various skeletal disorders such as osteoporosis, hypercalcemia of malignancy, tumor metastases and Paget's disease, bone resorption by osteoclasts exceeds bone formation by osteoblasts leading to decreased bone mass, skeletal fragility and bone fracture. The overall rate of osteoclastic bone resorption is regulated either at the level of differentiation of osteoclasts from their monocytic/macrophage precursor pool or through the regulation of key functional proteins whose specific activities in the mature osteoclast control its attachment, migration and resorption. Thus, reducing osteoclast numbers and/or decreasing the bone resorbing activity of osteoclasts are two common therapeutic approaches for the treatment of hyper-resorptive skeletal diseases. In this review, several of the key functional players involved in the regulation of osteoclast activity will be discussed.

Indexed as

AnimalsBone ResorptionCell AdhesionHumansModels, BiologicalOsteoclastsReceptor Activator of Nuclear Factor-kappa BReceptor, Macrophage Colony-Stimulating FactorReceptors, CalcitoninSignal TransductionReceptor Activator of Nuclear Factor-kappa BReceptor, Macrophage Colony-Stimulating FactorReceptors, Calcitonin

Identifiers

PMID16951988
OpenAlexW2068176262

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.