Evidence map›Paper›PMID 16571622›Full record

ArticleMolecular human reproduction2006

CCNs, fibulin-1C and S100A4 expression in leiomyoma and myometrium: inverse association with TGF-beta and regulation by TGF-beta in leiomyoma and myometrial smooth muscle cells.

Xiaoping Luo, Li Ding, Nasser Chegini

RetractedAbstract readRetracted Publication
PubMed Publisher
In one paragraph

Article in Molecular human reproduction, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. The role of the CCN family of proteins in female reproduction.Cellular and molecular life sciences : CMLS · 2014
    Review
  3. Article
  4. Transforming growth factor β signaling in uterine development and function.Journal of animal science and biotechnology · 2014
    Review
  5. A novel role of CCN3 in regulating endothelial inflammation.Journal of cell communication and signaling · 2010
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Xiaoping LuoDepartment of Obstetrics and Gynecology, University of Florida, Gainesville, 32610, USA.
Li Ding
Nasser Chegini
University of Florida · US

Funding

MOLECULAR MECHANISM OF LEIOMYOMA GROWTH AND REGRESSIONR01HD037432 · NICHD · UNIVERSITY OF FLORIDA · PI SCHULTZ, GREGORY SCOTT · 2001 to 2011
$2.7M
NICHD NIH HHS HD37432
6 · The paper itself

Abstract

Connective tissue growth factor (CTGF; CCN2) is considered to serve as downstream midiator of TGF-beta action in tissue fibrosis. We tested this hypothesis in paired leiomyoma and myometrium by evaluating the expression of TGF-beta1/TGF-beta3 and CCN2, the other members of the CCN family, CCN3 and CCN4, as well as fibulin-1C and S100A4, calcium-binding proteins that interact with CCNs. The regulatory function of TGF-beta1 on the expression of these genes was further evaluated using leiomyoma (L) and myometrial (M) smooth muscle cells (SMC). Real-time PCR, Western blotting and immunohistochemistry revealed that leiomyomas and myometrium express CCNs, fibulin-1C and S100A4, whose levels of expression with the exception of fibulin-1C were lower in leiomyomas and inversely correlated with the expression of TGF-beta1 and TGF-beta3 (P<0.05). The expression of these genes was menstrual cycle-independent and GnRHa therapy increased the expression of CCN2 in leiomyomas, while inhibiting CCN3, CCN4 and S100A4 in myometrium (P<0.05). TGF-beta (2.5 ng/ml) in a time- and cell-dependent manner, and through MAPK and Smad pathways, differentially regulated the expression of these genes in LSMC and MSMC. We concluded that CCNs, fibulin-1C and S100A4 are expressed in leiomyomas/myometrium with relative expression levels inversely correlating with TGF-betas and influenced by GnRHa and TGF-beta regulatory actions. The results suggest that unlike other fibrotic disorders, CCN2 (CTGF), at least at tissue level, may not serve as a downstream mediator of TGF-beta action in leiomyomas.

Indexed as

Blotting, WesternCalcium-Binding ProteinsCells, CulturedConnective Tissue Growth FactorFemaleGene ExpressionGonadotropin-Releasing HormoneHumansImmediate-Early ProteinsImmunohistochemistryIntercellular Signaling Peptides and ProteinsLeiomyomaMyocytes, Smooth MuscleMyometriumNephroblastoma Overexpressed ProteinRNA, MessengerCalcium-Binding ProteinsCCN2 protein, humanCCN3 protein, humanConnective Tissue Growth FactorfibulinGonadotropin-Releasing HormoneImmediate-Early ProteinsIntercellular Signaling Peptides and ProteinsNephroblastoma Overexpressed ProteinRNA, MessengerRNA, Small InterferingS100A4 protein, humanS100 Calcium-Binding Protein A4S100 ProteinsSmad3 ProteinTGFB1 protein, humanTransforming Growth Factor betaTransforming Growth Factor beta1Transforming Growth Factor beta3

Identifiers

PMID16571622
OpenAlexW2131250419

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.