Evidence map›Paper›PMID 25548487›Full record

ArticleWorld journal of gastroenterology2014

HIF-1α induces VE-cadherin expression and modulates vasculogenic mimicry in esophageal carcinoma cells.

Na-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

47 citing papers in PubMed, 56 citations in OpenAlex.

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  19. The role of microenvironment in tumor angiogenesis.Journal of experimental & clinical cancer research : CR · 2020
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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

10 authors at 2 institutions in 1 country.

Na-Na TangNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Hong ZhuNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Hong-Jie ZhangNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Wei-Feng ZhangNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Hai-Lin JinNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Lu WangNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Pin WangNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Gui-Jun HeNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Bo HaoNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Rui-Hua ShiNa-Na Tang, Hong Zhu, Hong-Jie Zhang, Wei-Feng Zhang, Hai-Lin Jin, Lu Wang, Pin Wang, Gui-Jun He, Bo Hao, Rui-Hua Shi, Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Nanjing Medical University · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate whether hypoxia inducible factor (HIF)-1α modulates vasculogenic mimicry (VM) by upregulating VE-cadherin expression in esophageal squamous cell carcinoma (ESCC).

methodsEsophageal squamous cancer cell lines Eca109 and TE13 were transfected with plasmids harboring small interfering RNAs targeting HIF-1α or VE-cadherin. The proliferation and invasion of esophageal carcinoma cells were detected by MTT and Transwell migration assays. The formation of tubular networks of cells was analyzed by 3D culture in vitro. BALB/c nude mice were used to observe xenograft tumor formation. The relationship between the expression of HIF-1α and VE-cadherin, ephrinA2 (EphA2) and laminin5γ2 (LN5γ2) was measured by Western blot and real-time polymerase chain reaction.

resultsKnockdown of HIF-1α inhibited cell proliferation (32.3% ± 6.1% for Eca109 cells and 38.6% ± 6.8% for TE13 cells, P < 0.05). Both Eca109 and TE13 cells formed typical tubular networks. The number of tubular networks markedly decreased when HIF-1α or VE-cadherin was knocked down. Expression of VE-cadherin, EphA2 and LN5γ2 was dramatically inhibited, but the expression of matrix metalloproteinase 2 had no obvious change in HIF-1α-silenced cells. Knockdown of VE-cadherin significantly decreased expression of both EphA2 and LN5γ2 (P < 0.05), while HIF-1α expression was unchanged. The time for xenograft tumor formation was 6 ± 1.2 d for Eca109 cells and Eca109 cells transfected with HIF-1α Neo control short hairpin RNA (shRNA) vector, and 8.4 ± 2.1 d for Eca109 cells transfected with an shRNA against HIF-1α. Knockdown of HIF-1α inhibited vasculogenic mimicry (VM) and tumorigenicity in vivo.

conclusionHIF-1α may modulate VM in ESCC by regulating VE-cadherin expression, which affects VM formation through EphA2 and LN5γ2.

Indexed as

Molecular MimicryNeovascularization, PathologicAnimalsAntigens, CDApoptosisCadherin 5CadherinsCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGene Expression Regulation, NeoplasticHumansAntigens, CDCadherin 5CadherinsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitLAMC2 protein, humanLamininReceptor, EphA2Esophageal squamous cell carcinomaHypoxia-inducible factor-1αRNA interferenceVasculogenic mimicryVE-cadherin

Identifiers

PMID25548487
PMCPMC4273139
OpenAlexW2309417538

What OpenQuestion holds

Textmetadata
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Registered trials

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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.