Evidence map›Paper›PMID 25534583›Full record

ArticleScientific reports2014

Comprehensive profiling analysis of actively resorbing osteoclasts identifies critical signaling pathways regulated by bone substrate.

P Edward Purdue, Tania N Crotti, Zhenxin Shen, Jennifer Swantek, Jun Li, Jonathan Hill, Adedayo Hanidu, Janice Dimock, Gerald Nabozny, Steven R Goldring and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The Role of Sphingolipid Metabolism in Bone Remodeling.Frontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Epigenetic regulation of bone cells.Connective tissue research · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. 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

11 authors at 5 institutions in 3 countries.

P Edward PurdueHospital for Special Surgery, New York, NY 10021.
Tania N Crotti1] School of Medical Sciences, The University of Adelaide, Adelaide 5005, Australia [2] Beth Israel Deaconess Medical Center, Boston, MA 02215.
Zhenxin ShenBeth Israel Deaconess Medical Center, Boston, MA 02215.
Jennifer SwantekBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Jun LiBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Jonathan HillBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Adedayo HaniduBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Janice DimockBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Gerald NaboznyBoehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, 06877.
Steven R GoldringHospital for Special Surgery, New York, NY 10021.
Kevin P McHughUniversity of Florida College of Dentistry, Gainesville, FL, 32610.
Boehringer Ingelheim (United States) · USHospital for Special Surgery · USBeth Israel Deaconess Medical Center · USFlorida College · USHadassah Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the only cells capable of efficiently resorbing bone, osteoclasts are central mediators of both normal bone remodeling and pathologies associates with excessive bone resorption. However, despite the clear evidence of interplay between osteoclasts and the bone surface in vivo, the role of the bone substrate in regulating osteoclast differentiation and activation at a molecular level has not been fully defined. Here, we present the first comprehensive expression profiles of osteoclasts differentiated on authentic resorbable bone substrates. This analysis has identified numerous critical pathways coordinately regulated by osteoclastogenic cytokines and bone substrate, including the transition from proliferation to differentiation, and sphingosine-1-phosphate signaling. Whilst, as expected, much of this program is dependent upon integrin beta 3, the pre-eminent mediator of osteoclast-bone interaction, a surprisingly significant portion of the bone substrate regulated expression signature is independent of this receptor. Together, these findings identify an important hitherto underappreciated role for bone substrate in osteoclastogenesis.

Indexed as

AnimalsBone ResorptionCell DifferentiationCell ProliferationGene Expression ProfilingGene Expression RegulationMiceOsteoclasts

Identifiers

PMID25534583
PMCPMC4274512
OpenAlexW1996216014

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.