Evidence map›Paper›PMID 22685266›Full record

ArticleEndocrine-related cancer2012

miR-200c is aberrantly expressed in leiomyomas in an ethnic-dependent manner and targets ZEBs, VEGFA, TIMP2, and FBLN5.

Tsai-Der Chuang, Harekrushna Panda, Xiaoping Luo, Nasser Chegini

Open access · bronzeAbstract read
In one paragraph

Article in Endocrine-related cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Transcriptomic and functional analysis of fibroid extracellular vesicles.Clinical science (London, England : 1979) · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Differential Expression of Small Non-Coding RNAs in Uterine Leiomyomas.International journal of molecular sciences · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
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  18. Article
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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 1 institution in 1 country.

Tsai-Der ChuangDepartment of Obstetrics and Gynecology, University of Florida, Gainesville, FL 32610-0294, USA. chuangtsaide@ufl.edu
Harekrushna Panda
Xiaoping Luo
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
Expression, hormonal regulation and function of microRNA in leiomyomaR01HD058664 · NICHD · UNIVERSITY OF FLORIDA · PI SCHULTZ, GREGORY SCOTT · 2009 to 2012
$1.4M
NICHD NIH HHS HD37432NICHD NIH HHS HD58664NICHD NIH HHS R01 HD037432NICHD NIH HHS R01 HD058664
6 · The paper itself

Abstract

MicroRNA-200c (miR-200c) through repression of specific target genes has been associated with cellular transition, tumorigenesis, and tissue fibrosis. We explored the expression and functional aspects of miR-200c in genesis of leiomyomas (LYO), benign uterine tumors with fibrotic characteristic. Using LYO and matched myometrium (MYO; n=76) from untreated and from patients exposed to hormonal therapies (GNRH agonist (GNRHa), Depo-Provera, and oral contraceptives), we found that miR-200c was expressed at significantly lower levels (P<0.05) in LYO as compared with MYO. These levels were lower in LYO from African Americans as compared with Caucasians, patients experiencing abnormal uterine bleeding and those exposed to GNRHa therapy. Gain-of-function of miR-200c in isolated leiomyoma smooth muscle cells (LSMCs), myometrial smooth muscle cells (MSMCs), and leiomyosarcoma cell line (SKLM-S1) repressed ZEB1/ZEB2 mRNAs and proteins, with concurrent increase in E-cadherin (CDH1) and reduction in vimentin expression, phenotypic alteration, and inhibition of MSMC and LSMC proliferations. We further validated TIMP2, FBLN5, and VEGFA as direct targets of miR-200c through interaction with their respective 3' UTRs, and other genes as determined by microarray analysis. At tissue levels, LYO expressed lower levels of TIMP2 and FBLN5 mRNAs but increased protein expressions, which to some extent altered due to hormonal exposure. Given the regulatory functions of ZEBs, VEGFA, FBLN5, and TIMP2 on cellular activities that promote cellular transition, angiogenesis, and matrix remodeling, we concluded that altered expression of miR-200c may have a significant impact on the outcome of LYO growth, maintenance of their mesenchymal and fibrotic characteristics, and possibly their associated symptoms.

Indexed as

AdultCase-Control StudiesEthnicityExtracellular Matrix ProteinsFemaleGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansLeiomyomaMicroRNAsMiddle AgedRepressor ProteinsTissue Inhibitor of Metalloproteinase-2Transcription FactorsUterine NeoplasmsVascular Endothelial Growth Factor AExtracellular Matrix ProteinsFBLN5 protein, humanHomeodomain ProteinsMicroRNAsMIRN200 microRNA, humanRepressor ProteinsTIMP2 protein, humanTissue Inhibitor of Metalloproteinase-2Transcription FactorsVascular Endothelial Growth Factor AVEGFA protein, humanZEB1 protein, humanZEB2 protein, humanZinc Finger E-box-Binding Homeobox 1Zinc Finger E-box Binding Homeobox 2

Identifiers

PMID22685266
PMCPMC3402184
OpenAlexW2116286448

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.