Evidence map›Paper›PMID 30416855›Full record

ArticleAmerican journal of cancer research2018

VEGF-C/Flt-4 axis in tumor cells contributes to the progression of oral squamous cell carcinoma via upregulating VEGF-C itself and contactin-1 in an autocrine manner.

Seiji Shigetomi, Yorihisa Imanishi, Katsushi Shibata, Nobuya Sakai, Koji Sakamoto, Ryoichi Fujii, Noboru Habu, Kuninori Otsuka, Yoichiro Sato, Yoshihiro Watanabe and 5 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Thrombosis Risk Associated with Head and Neck Cancer: A Review.International journal of molecular sciences · 2019
    Review
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

15 authors at 2 institutions in 1 country.

Seiji ShigetomiDepartment of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Keio University Tokyo, Japan.
Yorihisa ImanishiDepartment of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Keio University Tokyo, Japan.
Katsushi ShibataDepartment of Functional Genomics, Faculty of Pharmaceutical Sciences, Himeji Dokkyo University Himeji, Japan.
Nobuya SakaiDepartment of Functional Genomics, Faculty of Pharmaceutical Sciences, Himeji Dokkyo University Himeji, Japan.
Koji SakamotoDepartment of Otorhinolaryngology-Head and Neck Surgery, Saiseikai Utsunomiya Hospital Utsunomiya, Japan.
Ryoichi FujiiDepartment of Otorhinolaryngology, Saiseikai Yokohamashi Tobu Hospital Yokohama, Japan.
Noboru HabuDepartment of Otorhinolaryngology, Kyosai Tachikawa Hospital Tokyo, Japan.
Kuninori OtsukaDepartment of Otorhinolaryngology, Shin-Yurigaoka General Hospital Kawasaki, Japan.
Yoichiro SatoDepartment of Otorhinolaryngology-Head and Neck Surgery, Kawasaki Municipal Kawasaki Hospital Kawasaki, Japan.
Yoshihiro WatanabeDepartment of Otorhinolaryngology, Tokyo Saiseikai Central Hospital Tokyo, Japan.
Masayuki ShimodaDepartment of Pathology, School of Medicine, Keio University Tokyo, Japan.
Kaori KameyamaDepartment of Pathology, School of Medicine, Keio University Tokyo, Japan.
Hiroyuki OzawaDepartment of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Keio University Tokyo, Japan.
Toshiki TomitaDepartment of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Keio University Tokyo, Japan.
Kaoru OgawaDepartment of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Keio University Tokyo, Japan.
Keio University · JPHimeji Dokkyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor cell-derived vascular endothelial growth factor (VEGF)-C has been primarily implicated in promoting lymphangiogenesis by activating Flt-4 (VEGFR-3) expressed on lymphatic endothelial cells via a paracrine mechanism. Flt4 has also been shown to be expressed selectively in subsets of cancer cells. However, little is known about the functional role of VEGF-C/Flt4 signaling via an autocrine mechanism, as well as the clinicopathological implication of the VEGF-C/Flt4 axis and its downstream effector molecules, in head and neck squamous cell carcinoma (HNSCC), including oral squamous cell carcinoma (OSCC). In the present study, we detected Flt-4 expression selectively in several HNSCC cell lines by quantitative PCR, and its internalization reflecting receptor activation was confirmed by immunocytochemistry in SAS and HO1U1 cells. Flt-4 stimulation upregulated the expression of contactin-1 (CNTN-1, a neural cell adhesion molecule) and VEGF-C itself in SAS cells, while Flt-4 inhibition downregulated the expression of CNTN-1 in both SAS and HO1U1 cells and that of VEGF-C itself in SAS cells.

Indexed as

autocrine mannercontactin-1Flt-4metastasismigrationoral squamous cell carcinomaproliferationtumor cellVEGF-C

Identifiers

PMID30416855
PMCPMC6220132
OpenAlexW2969721714

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.