Evidence map›Paper›PMID 17051438›Full record

ReviewReviews in endocrine & metabolic disorders2006

Networks and hubs for the transcriptional control of osteoblastogenesis.

Jane B Lian, Gary S Stein, Amjad Javed, Andre J van Wijnen, Janet L Stein, Martin Montecino, Mohammad Q Hassan, Tripti Gaur, Christopher J Lengner, Daniel W Young

Abstract 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. Cited by 212 papers.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

212 citing papers in PubMed, 470 citations in OpenAlex.

  1. Trial
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  3. Article
  4. Review
  5. Review
  6. Air Pollution and Osteoporosis.Current osteoporosis reports · 2024
    Review
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  14. Article
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  17. Review
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152 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

10 authors at 3 institutions in 2 countries.

Jane B LianDepartment of Cell Biology and Cancer Center, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA. jane.lian@umassmed.edu
Gary S Stein
Amjad Javed
Andre J van Wijnen
Janet L Stein
Martin Montecino
Mohammad Q Hassan
Tripti Gaur
Christopher J Lengner
Daniel W Young
University of Massachusetts Chan Medical School · USUniversity of Alabama at Birmingham · USUniversity of Concepción · CL

Funding

Subnuclear Integration of Regulatory Signals Controlling Bone Cell FunctionP01AR048818 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, JANET L · 2002 to 2011
$14.0M
CONTROL OF OSTEOBLAST PROLIFERATION AND DIFFERENTIATIONR01AR039588 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B., STEIN, GARY S. · 1990 to 2019
$8.0M
Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Synthesis of Osteocalcin in BoneR37DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B. · 2008 to 2017
$5.0M
SYNTHESIS OF OSTEOCALCIN IN BONER01DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B · 1997 to 2006
$2.6M
NIAMS NIH HHS AR39588NIAMS NIH HHS P01 AR48818NIAMS NIH HHS R01 AR049069NIDCR NIH HHS DE12528
6 · The paper itself

Abstract

We present an overview of the concepts of tissue-specific transcriptional control mechanisms essential for development of the bone cell phenotype. BMP2 induced transcription factors constitute a network of activities and molecular switches for bone development and osteoblast differentiation. Among these regulators are Runx2 (Cbfa1/AML3), the principal osteogenic master gene for bone formation, as well as homeodomain proteins and osterix. Runx2 has multiple regulatory activities, including activation or repression of gene expression, and integration of biological signals from developmental cues, such as BMP/TGFbeta, Wnt and Src signaling pathways. Runx2 provides a new paradigm for transcriptional control by functioning as a principal scaffolding protein in nuclear microenvironments to control gene expression in response to physiologic signals (growth factors, cytokines and hormones). The protein serves as a hub for the coordination of activities essential for the expansion and differentiation of osteogenic lineage cells through the formation of co-regulatory protein complexes organized in subnuclear domains. Mechanisms by which Runx2 supports commitment to osteogenesis and determines cell fate involve its retention on mitotic chromosomes. Disruption of a unique protein module, the subnuclear targeting signal of Runx2, has profound effects on osteoblast differentiation and metastasis of cancer cells in the bone microenvironment. Runx2 target genes include regulators of cell growth control, components of the bone extracellular matrix, angiogenesis, and signaling proteins for development of the osteoblast phenotype and bone turnover. The specificity of Runx2 regulatory activities provides a basis for novel therapeutic strategies to correct bone disorders.

Indexed as

Gene Regulatory NetworksAnimalsBone Morphogenetic ProteinsBone NeoplasmsCarcinomaCell DifferentiationCore Binding Factor Alpha 1 SubunitGene Expression Regulation, DevelopmentalHumansModels, BiologicalNeoplasm MetastasisOsteoblastsOsteogenesisSignal TransductionSmad ProteinsWnt ProteinsBone Morphogenetic ProteinsCore Binding Factor Alpha 1 SubunitSmad ProteinsWnt Proteins

Identifiers

PMID17051438
OpenAlexW2068627477

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.