Evidence map›Paper›PMID 27901498›Full record

ReviewOncotarget2017

Targeting the VEGF-C/VEGFR3 axis suppresses Slug-mediated cancer metastasis and stemness via inhibition of KRAS/YAP1 signaling.

Yu-Wen Yeh, Ching-Chia Cheng, Shu-Ting Yang, Chi-Feng Tseng, Ting-Yu Chang, Sin-Ying Tsai, Earl Fu, Chien-Ping Chiang, Li-Chuan Liao, Pei-Wen Tsai and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  9. Metastasis and MAPK Pathways.International journal of molecular sciences · 2022
    Review
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  11. Advances in 3D Vascularized Tumor-on-a-Chip Technology.Advances in experimental medicine and biology · 2022
    Article
  12. Review
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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

12 authors at 6 institutions in 1 country.

Yu-Wen YehDivision of Dermatology, Tri-Service General Hospital Songshan Branch, National Defense Medical Center, Taipei 10581, Taiwan.
Ching-Chia ChengGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 11490, Taiwan.
Shu-Ting YangNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Miaoli County 35053, Taiwan.
Chi-Feng TsengNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Miaoli County 35053, Taiwan.
Ting-Yu ChangNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Miaoli County 35053, Taiwan.
Sin-Ying TsaiDepartment of Biotechnology, Asia University, Taichung 41354, Taiwan.
Earl FuDepartment of Periodontology, Tri-Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan.
Chien-Ping ChiangDepartment of Dermatology, Tri-Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan.
Li-Chuan LiaoBioresource Collection and Research Center, Food Industry Research and Development Institute, Hsinchu 30062, Taiwan.
Pei-Wen TsaiInstitute of Molecular and Cellular Biology, National Tsing Hua University, Hsinchu 30013, Taiwan.
Yung-Luen YuDepartment of Biotechnology, Asia University, Taichung 41354, Taiwan.
Jen-Liang SuNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Miaoli County 35053, Taiwan.
National Health Research Institutes · TWAsia University · TWNational Defense Medical Center · TWTri-Service General Hospital · TWFood Industry Research and Development Institute · TWNational Tsing Hua University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular endothelial growth factor-C (VEGF-C) has been implicated in epithelial-mesenchymal transition (EMT) processes and various human cancers, including skin cancer. Skin cancer is an aggressive human malignancy with increasing incidence worldwide; however, the underlying mechanisms involved in VEGF-C-induced skin cancer stemness and metastasis remain unclear. Here, we report that VEGF-C enhances skin cancer migration, invasion and stemness through Slug up-regulation. Oncomine database analysis indicated that the KRAS/MAPK (mitogen-activated protein kinases) pathway and YAP1 (yes-associated protein 1) expression are positively correlated with metastatic skin cancer. We show that VEGF-C triggers the activation of KRAS/MAPK signaling to increase YAP1 and downstream Slug expression, which are suppressed by an anti-VEGFR3 (VEGF receptor 3) peptide, a specific peptide targeting VEGFR3. The VEGF-C-induced migration, invasion and stemness of skin cancer cells are also abrogated by the anti-VEGFR3 peptide. Based on these data, we reveal the role of the VEGF-C/VEGFR3-mediated KRAS/MAPK-YAP1/Slug pathway in skin cancer progression and propose that the VEGF-C/VEGFR3 axis is a promising target for the anti-VEGFR3 peptide.

Indexed as

Cell MovementHumansNeoplasm InvasivenessNeoplastic Stem CellsSignal TransductionSkin NeoplasmsSnail Family Transcription FactorsVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3FLT4 protein, humanSNAI1 protein, humanSnail Family Transcription FactorsVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3cancer stemnessmetastasisskin cancerVEGF-CYAP1

Identifiers

PMID27901498
PMCPMC5354933
OpenAlexW2555008614

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.