Evidence map›Paper›PMID 18535099›Full record

ArticleEndocrinology2008

Skeletal overexpression of connective tissue growth factor impairs bone formation and causes osteopenia.

Anna Smerdel-Ramoya, Stefano Zanotti, Lisa Stadmeyer, Deena Durant, Ernesto Canalis

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  12. E-selectin ligand 1 regulates bone remodeling by limiting bioactive TGF-β in the bone microenvironment.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
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  16. Review
  17. CCN family 2/connective tissue growth factor (CCN2/CTGF) promotes osteoclastogenesis via induction of and interaction with dendritic cell-specific transmembrane protein (DC-STAMP).Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  18. Article
  19. WISP-1/CCN4 regulates osteogenesis by enhancing BMP-2 activity.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  20. The role of connective tissue growth factor (CTGF/CCN2) in skeletogenesis.Critical reviews in eukaryotic gene expression · 2011
    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

5 authors at 2 institutions in 1 country.

Anna Smerdel-RamoyaDepartment of Research, Saint Francis Hospital and Medical Center, 114 Woodland Street, Hartford, Connecticut 06105-1299, USA.
Stefano Zanotti
Lisa Stadmeyer
Deena Durant
Ernesto Canalis
Saint Francis Hospital & Medical Center · USSaint Francis University · US

Funding

Mechanisms of Notch Action in BoneR01DK045227 · NIDDK · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CANALIS, ERNESTO · 1991 to 2018
$4.7M
Growth Factors; Effect on Aspects of Bone FormationR01AR021707 · NIAMS · ST. FRANCIS HOSPITAL AND MEDICAL CENTER · PI CANALIS, ERNESTO · 1986 to 2012
$2.5M
SOMATOMEDIN-AUTOLOGOUS REGULATOR OF BONE FORMATIONR01DK042424 · NIDDK · ST. FRANCIS HOSPITAL AND MEDICAL CENTER · PI CANALIS, ERNESTO · 1989 to 2008
$1.5M
GROWTH FACTORS EFFECT ON ASPECTS OF BONE FORMATIONR37AR021707 · NIAMS · ST. FRANCIS HOSPITAL AND MEDICAL CENTER · PI CANALIS, ERNESTO · 1992 to 2001
$624k
NIAMS NIH HHS AR021707NIAMS NIH HHS R01 AR021707NIAMS NIH HHS R37 AR021707NIDDK NIH HHS DK042424NIDDK NIH HHS DK045227NIDDK NIH HHS R01 DK042424NIDDK NIH HHS R01 DK045227
6 · The paper itself

Abstract

Connective tissue growth factor (CTGF), a member of the CCN family of proteins, is expressed in skeletal cells, and the ctgf null mutation leads to neonatal lethality due to defects in skeletal development. To define the function of CTGF in the postnatal skeleton, we created transgenic mice overexpressing CTGF under the control of the human osteocalcin promoter. CTGF transgenic female and male mice exhibited a significant decrease in bone mineral density, compared with wild-type littermate controls. Bone histomorphometry revealed that CTGF overexpression caused decreased trabecular bone volume due to impaired osteoblastic activity because mineral apposition and bone formation rates were decreased. Osteoblast and osteoclast number and bone resorption were not altered. Calvarial osteoblasts and stromal cells from CTGF transgenics displayed decreased alkaline phosphatase and osteocalcin mRNA levels and reduced bone morphogenetic protein (BMP) signaling mothers against decapentaplegic, Wnt/beta-catenin, and IGF-I/Akt signaling. In conclusion, CTGF overexpression in vivo causes osteopenia, secondary to decreased bone formation, possibly by antagonizing BMP, Wnt, and IGF-I signaling and activity.

Indexed as

AnimalsBone and BonesBone Diseases, MetabolicBone Morphogenetic ProteinsCells, CulturedConnective Tissue Growth FactorEmbryo, MammalianFemaleGene Expression Regulation, DevelopmentalImmediate-Early ProteinsInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsMiceMice, TransgenicOsteoblastsOsteocalcinBone Morphogenetic ProteinsCCN2 protein, humanCCN2 protein, mouseConnective Tissue Growth FactorImmediate-Early ProteinsInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsOsteocalcinWnt Proteins

Identifiers

PMID18535099
PMCPMC2553373
OpenAlexW2170184391

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.