Evidence map›Paper›PMID 20703218›Full record

ReviewNature reviews. Rheumatology2010

Novel functions for NFκB: inhibition of bone formation.

Susan A Krum, Jia Chang, Gustavo Miranda-Carboni, Cun-Yu Wang

Abstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

84 citing papers in PubMed, 153 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
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  9. Article
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  11. Article
  12. Review
  13. Article
  14. Review
  15. Herpesvirus-Entry Mediator Inhibits the NF-Journal of tissue engineering and regenerative medicine · 2024
    Article
  16. Article
  17. Aging under endocrine hormone regulation.Frontiers in endocrinology · 2023
    Review
  18. Article
  19. Article
  20. Review

24 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

4 authors at 2 institutions in 1 country.

Susan A KrumUCLA Orthopaedic Hospital, Department of Orthopaedic Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Jia Chang
Gustavo Miranda-Carboni
Cun-Yu Wang
University of California, Los Angeles · USUCLA Jonsson Comprehensive Cancer Center

Funding

Molecular Regulation of Human Dental Stem Cell PropertyR01DE016513 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, CUN-YU · 2005 to 2019
$6.0M
Wnt-4 inhibits peridontitis by attenuating NF-kBR01DE019412 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2008 to 2021
$5.7M
Building Interdisciplinary Research Careers in Women's Health (BIRCWH) CenterK12HD001400 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHAUDHURI, GAUTAM · 2000 to 2009
$4.2M
PS-341-induced Apoptosis in Squamous Cell CarcinomaR37DE013848 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, CUN-YU · 2006 to 2015
$3.5M
Inhibition of Bone Formation by TNF/NF-kappa B SignalingR01DE017684 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2008 to 2011
$1.4M
TNF-ALPHA-MEDIATED APOPTOSIS IN SQUAMOUS CELL CARCINOMAR01DE013848 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, CUN-YU · 2000 to 2004
$1.4M
Regulation of Oncogenesis and Apoptosis by WntR01CA100849 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, CUN-YU · 2004 to 2007
$1.1M
Wnt10b's Functional Role on Mammary Stem CellsK22CA137168 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MIRANDA-CARBONI, GUSTAVO ADOLFO · 2009 to 2011
$564k
NCI NIH HHS CA100849NCI NIH HHS K22 CA137168NCI NIH HHS R01 CA100849NICHD NIH HHS K12 HD001400NICHD NIH HHS K12 HD001400‑08NIDCR NIH HHS DE016513NIDCR NIH HHS DE019412NIDCR NIH HHS DE13848NIDCR NIH HHS DE17684NIDCR NIH HHS R01 DE013848NIDCR NIH HHS R01 DE016513NIDCR NIH HHS R01 DE017684NIDCR NIH HHS R01 DE019412NIDCR NIH HHS R37 DE013848
6 · The paper itself

Abstract

NFκB is a family of transcription factors involved in immunity and the normal functioning of many tissues. It has been well studied in osteoclasts, and new data indicate an important role for NFκB in the negative regulation of bone formation. In this article, we discuss how NFκB activation affects osteoblast function and bone formation. In particular, we describe how reduced NFκB activity in osteoblasts results in an increase in bone formation via enhanced c-Jun N-terminal kinase (JNK) activity, which regulates FOSL1 (also known as Fra1) expression. Furthermore, we discuss how estrogen and NFκB crosstalk in osteoblasts acts to oppositely regulate bone formation. Future NFκB-targeting treatments for osteoporosis, rheumatoid arthritis and other inflammatory bone diseases could lead to increased bone formation concurrent with decreased bone resorption.

Indexed as

AnimalsCell DifferentiationCell LineEstradiolFos-Related Antigen 1Gene ExpressionHumansJNK Mitogen-Activated Protein KinasesMiceMice, KnockoutNF-kappa BOsteoblastsOsteoclastsOsteogenesisOvariectomyProto-Oncogene Proteins c-fosEstradiolFos-Related Antigen 1JNK Mitogen-Activated Protein KinasesNF-kappa BProto-Oncogene Proteins c-fosTumor Necrosis Factor-alpha

Identifiers

PMID20703218
PMCPMC3078572
OpenAlexW2004316687

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.