Evidence map›Paper›PMID 25486362›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Autophagy functions on EMT in gastrulation of avian embryo.

Wen-Hui Lu, Guang Wang, Yan Li, Shuai Li, Xiao-Yu Song, Xiao-Yu Wang, Manli Chuai, Kenneth Ka Ho Lee, Liu Cao, Xuesong Yang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  10. Autophagy-related 7 modulates tumor progression in triple-negative breast cancer.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
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  13. Review
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  19. Snail promotes epithelial-mesenchymal transition and invasiveness in human ovarian cancer cells.International journal of clinical and experimental medicine · 2015
    Article
  20. 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

10 authors at 2 institutions in 2 countries.

Wen-Hui Lua Key Laboratory for Regenerative Medicine of the Ministry of Education; Division of Histology and Embryology; Medical College ; Jinan University ; Guangzhou , China.
Guang Wang
Yan Li
Shuai Li
Xiao-Yu Song
Xiao-Yu Wang
Manli Chuai
Kenneth Ka Ho Lee
Liu Cao
Xuesong Yang
Chinese University of Hong Kong · CNUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is important for cell renewing for its contribution to the degradation of bulk cytoplasm, long-lived proteins, and entire organelles and its role in embryonic development is largely unknown. In our study, we investigated the function of autophagy in gastrulation of the chick embryo using both in vivo and in vitro approaches, especially in the EMT process, and we found that autophagy gene Atg7 was expressed on the apical side of the ectoderm and endoderm. Over-expression of Atg7 could enhance the expression of Atg8 and the E-cadherin, the latter of which is a crucial marker of the EMT process. We also found that the disturbance of autophagy could retard the development of chick embryos in HH4 with shorter primitive steak than that in the control group, which is a newly formed structure during EMT process. So we assumed that autophagy could affect EMT process by adhesion molecule expression. Moreover, more molecules, such as slug, chordin, shh et., which were all involved in EMT process, were detected to address the mechanism of this phenomena. We established that the inhibition of autophagy could cause developmental delay by affecting EMT process in gastrulation of chick embryos.

Indexed as

AutophagyEpithelial-Mesenchymal TransitionGastrulationAdenineAnimalsCadherinsCell Adhesion MoleculesChick EmbryoGastrulaGene Expression Regulation, DevelopmentalGerm LayersHCT116 CellsHumansMicrotubule-Associated ProteinsModels, BiologicalSirolimus3-methyladenineAdenineCadherinsCell Adhesion MoleculesMicrotubule-Associated ProteinsSirolimus3-MA, 3-MethyladenineAtg7autophagyBF, bright-fieldDAPI, 49-6-Diamidino-2-phenylindoleEB, embryoid bodiesE-Cad, E-cadherinEMT and chick embryoEMTs, epithelial-mesenchymal transitionsgastrulationGFP, green fluorescent proteinHN, Hensen's nodeMAPILC3(LC3), microtubule-associated protein 1 light chain 3mTOR, mammalian target of rapamycinN-Cad, N-cadherinNT, neural tubePBS, phosphate-buffered salinePCD, Programmed cell deathPD, idiopathic Parkinson's DiseasePI3K, phosphoinositide-3-kinasePPIA, peptidylprolyl isomerase APS, primitive streakRAPA, RapamycinRT-PCR, reverse transcription PCRshh, sonic hedgehog

Identifiers

PMID25486362
PMCPMC4615036
OpenAlexW2034771046

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.