Evidence map›Paper›PMID 35997849›Full record

ArticleIn vitro cellular & developmental biology. Animal2022

VEGF-A promotes the motility of human melanoma cells through the VEGFR1-PI3K/Akt signaling pathway.

Koichi Koizumi, Tomoaki Shintani, Yasutaka Hayashido, Atsuko Hamada, Mirai Higaki, Yukio Yoshioka, Akihiko Sakamoto, Souichi Yanamoto, Tetsuji Okamoto

Open access · hybridAbstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. VEGFR1 as a Target for Cardiovascular Gene Therapy.Journal of cardiovascular translational research · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Regulation of VEGF-A expression and VEGF-A-targeted therapy in malignant tumors.Journal of cancer research and clinical oncology · 2024
    Review
  10. Review
  11. Molecular Imaging of Melanoma VEGF-expressing Tumors through [Anti-cancer agents in medicinal chemistry · 2024
    Article
  12. Article
  13. 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

9 authors at 2 institutions in 1 country.

Koichi Koizumi *Department of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.
Tomoaki Shintani *Center of Oral Clinical Examination, Hiroshima University Hospital, Hiroshima, 734-8551, Japan.
Yasutaka HayashidoOral Maxillofacial Surgery, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan. hayashiy@hiroshima-u.ac.jp.
Atsuko HamadaOral Maxillofacial Surgery, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.
Mirai HigakiOral Maxillofacial Surgery, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.
Yukio YoshiokaDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.
Akihiko SakamotoOral Maxillofacial Surgery, Hiroshima University Hospital, Hiroshima, 734-8551, Japan.
Souichi YanamotoDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.
Tetsuji OkamotoDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.
Hiroshima University Hospital · JPHiroshima University · JP

Funding

Grants-in-Aid for Scientific Research (B) from the Japanese Ministry of Education, Culture, Sports, Science and Technology 18H03000Grants-in-Aid for Scientific Research (C) from the Japanese Ministry of Education, Culture, Sports, Science and Technology 24593033
6 · The paper itself

Abstract

Vascular endothelial growth factor A (VEGF-A) and its receptors (VEGFR1 and R2) play important roles in the progression of malignant melanoma through tumor angiogenesis. However, it is not clear whether the VEGF-A/VEGFR1 signaling pathway is involved in the proliferation and migration of melanoma cells. Thus, the effect of VEGF-A on cell migration was investigated in human melanoma cell lines. Of several splicing variants of VEGF-A, VEGF

Indexed as

MelanomaVascular Endothelial Growth Factor AAnimalsAntibodies, NeutralizingCell MovementHumansOligonucleotides, AntisensePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPhosphatidylinositolsProto-Oncogene Proteins c-aktSignal TransductionWortmanninAntibodies, NeutralizingOligonucleotides, AntisensePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPhosphatidylinositolsProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor AWortmanninCell motilityMelanomaPI3K/Akt signaling pathwayVEGF-AVEGFR1

Identifiers

PMID35997849
PMCPMC9550759
OpenAlexW4292756245

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.