Evidence map›Paper›PMID 37286356›Full record

ArticleAging2023

Visfatin upregulates VEGF-C expression and lymphangiogenesis in esophageal cancer by activating MEK1/2-ERK and NF-κB signaling.

Chang-Lun Huang, David Achudhan, Po-I Liu, Yen-You Lin, Shan-Chi Liu, Jeng-Hung Guo, Chun-Lin Liu, Chih-Ying Wu, Shih-Wei Wang, Chih-Hsin Tang

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Genetic associations ofInternational journal of medical sciences · 2024
    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 6 institutions in 1 country.

Chang-Lun HuangGraduate Institute of Biomedical Science, College of Medicine, China Medical University, Taichung 40402, Taiwan.
David AchudhanGraduate Institute of Biomedical Science, College of Medicine, China Medical University, Taichung 40402, Taiwan.
Po-I LiuDepartment of General Thoracic Surgery, Asia University Hospital, Taichung 41354, Taiwan.
Yen-You LinDepartment of Pharmacology, School of Medicine, China Medical University, Taichung 40402, Taiwan.
Shan-Chi LiuDepartment of Medical Education and Research, China Medical University Beigang Hospital, Yunlin 65152, Taiwan.
Jeng-Hung GuoGraduate Institute of Biomedical Science, College of Medicine, China Medical University, Taichung 40402, Taiwan.
Chun-Lin LiuGraduate Institute of Biomedical Science, College of Medicine, China Medical University, Taichung 40402, Taiwan.
Chih-Ying WuDepartment of Neurosurgery, China Medical University Hospital, Taichung 404327, Taiwan.
Shih-Wei WangDepartment of Medicine, Mackay Medical College, New Taipei 252, Taiwan.
Chih-Hsin TangGraduate Institute of Biomedical Science, College of Medicine, China Medical University, Taichung 40402, Taiwan.
China Medical University · TWChina Medical University Hospital · TWAsia University · TWChanghua Christian Hospital · TWChina Medical University Beigang Hospital · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymph node metastasis is a recognized prognostic factor in esophageal cancer. Adipokines, including visfatin, and the molecule vascular endothelial growth factor (VEGF)-C, are implicated in lymphangiogenesis, but whether any association exists between esophageal cancer, adipokines and VEGF-C is unknown. We examined the relevance of adipokines and VEGF-C in esophageal squamous cell carcinoma (ESCC) in the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) databases. We found significantly higher levels of visfatin and VEGF-C expression in esophageal cancer tissue than in normal tissue. Immunohistochemistry (IHC) staining identified that higher levels of visfatin and VEGF-C expression were correlated with advanced stage ESCC. Visfatin treatment of ESCC cell lines upregulated VEGF-C expression and VEGF-C-dependent lymphangiogenesis in lymphatic endothelial cells. Visfatin induced increases in VEGF-C expression by activating the mitogen-activated protein kinase kinases1/2-extracellular signal-regulated kinase (MEK1/2-ERK) and Nuclear Factor Kappa B (NF-κB) signaling cascades. Transfecting ESCC cells with MEK1/2-ERK and NF-κB inhibitors (PD98059, FR180204, PDTC, and TPCK) and siRNAs inhibited visfatin-induced increases in VEGF-C expression. It appears that visfatin and VEGF-C are promising therapeutic targets in the inhibition of lymphangiogenesis in esophageal cancer.

Indexed as

Esophageal NeoplasmsEsophageal Squamous Cell CarcinomaAdipokinesEndothelial CellsHumansLymphangiogenesisNF-kappa BNicotinamide PhosphoribosyltransferaseVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CAdipokinesNF-kappa BNicotinamide PhosphoribosyltransferaseVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CcanceresophageallymphangiogenesisVEGF-Cvisfatin

Identifiers

PMID37286356
PMCPMC10292883
OpenAlexW4379744254

What Socratic 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 Socratic graph.