Evidence map›Paper›PMID 22223649›Full record

ArticleThe Journal of biological chemistry2012

Cell division cycle 7 is a novel regulator of transforming growth factor-β-induced smooth muscle cell differentiation.

Ning Shi, Wei-Bing Xie, Shi-You Chen

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. TRPC6-Mediated ZnBiomolecules · 2025
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  4. TRPC6 regulates phenotypic switching of vascular smooth muscle cells through plasma membrane potential-dependent coupling with PTEN.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  5. Article
  6. Lack of Association of rs1192415 inFrontiers in genetics · 2018
    Article
  7. Article
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  9. Article
  10. CYLD-mediated signaling and diseases.Current drug targets · 2015
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
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

3 authors at 1 institution in 1 country.

Ning ShiDepartment of Physiology & Pharmacology, University of Georgia, Athens, Georgia 30602, USA.
Wei-Bing Xie
Shi-You Chen
University of Georgia · US

Funding

Smad2 and Smooth Muscle Differentiation from Neural Crest Stem CellsR01HL093429 · NHLBI · UNIVERSITY OF GEORGIA · PI CHEN, SHIYOU · 2008 to 2013
$2.0M
Smooth Muscle Differentiation and MaturationR01HL107526 · NHLBI · UNIVERSITY OF GEORGIA · PI CHEN, SHIYOU · 2011 to 2014
$1.5M
NHLBI NIH HHS HL107526NHLBI NIH HHS R01 HL093429NHLBI NIH HHS R01 HL107526
6 · The paper itself

Abstract

Smooth muscle cell (SMC) differentiation and proliferation occur simultaneously during embryonic development. The underlying mechanisms especially common factors regulating both processes, however, remain largely unknown. The present study has identified cell division cycle 7 (Cdc7) as one of the factors mediating both the proliferation and SMC differentiation. TGF-β induces Cdc7 expression and phosphorylation in the initial phase of SMC differentiation of pluripotent mesenchymal C3H10T1/2 cells. Cdc7 specific inhibitor or shRNA knockdown suppresses TGF-β-induced expression of SMC early markers including α-SMA, SM22α, and calponin. Cdc7 overexpression, on the other hand, enhances SMC marker expression. Cdc7 function in inducing SMC differentiation is independent of Dumbbell former 4 or Dbf4, the catalytic subunit of Cdc7 critical for cell proliferation, suggesting that Cdc7 mediates SMC differentiation through a mechanism distinct from cell proliferation. Cdc7 regulates SMC differentiation via activating SMC marker gene transcription. Knockdown of Cdc7 by shRNA inhibits SMC marker gene promoter activities. Mechanistically, Cdc7 interacts with Smad3 to induce SMC differentiation. Smad3 is required for Cdc7 function in inducing SMC promoter activities and marker gene expression. Likewise, Cdc7 enhances Smad3 binding to SMC marker promoter via supporting Smad3 nuclear retention and physically interacting with Smad3. Taken together, our studies have demonstrated a novel role of Cdc7 in SMC differentiation.

Indexed as

AnimalsBiomarkersCell Cycle ProteinsCell DifferentiationCell DivisionCell LineFibroblastsGene Expression Regulation, DevelopmentalMiceMyocytes, Smooth MusclePluripotent Stem CellsPromoter Regions, GeneticProtein Serine-Threonine KinasesRNA, Small InterferingSignal TransductionSmad3 ProteinBiomarkersCdc7 protein, mouseCell Cycle ProteinsDBF4 protein, mouseProtein Serine-Threonine KinasesRNA, Small InterferingSmad3 ProteinSmad3 protein, mouseTgfb1 protein, mouseTransforming Growth Factor beta1

Identifiers

PMID22223649
PMCPMC3307322
OpenAlexW2070317129

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.