Evidence map›Paper›PMID 33466636›Full record

ArticleInternational journal of molecular sciences2021

Effects of 6,8-Diprenylgenistein on VEGF-A-Induced Lymphangiogenesis and Lymph Node Metastasis in an Oral Cancer Sentinel Lymph Node Animal Model.

Mun Gyeong Bae, Jeon Hwang-Bo, Dae Young Lee, Youn-Hyung Lee, In Sik Chung

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. EGR1 Enhances Lymphangiogenesis via SOX18-Mediated Activation of JAK2/STAT3 Pathway.Computational and mathematical methods in medicine · 2022
    Article
  7. Effects ofMolecules (Basel, Switzerland) · 2021
    Article
  8. Article
  9. 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

5 authors at 1 institution in 1 country.

Mun Gyeong BaeDepartment of Genetic Engineering and Graduate School of Biotechnology, Kyung Hee University, Yongin 446-701, Korea.
Jeon Hwang-BoDepartment of Genetic Engineering and Graduate School of Biotechnology, Kyung Hee University, Yongin 446-701, Korea.
Dae Young LeeDepartment of Herbal Crop Research, National Institute of Horticulture and Herbal Science, RDA, Eumseong 27709, Korea.ORCID 0000-0003-4302-3096
Youn-Hyung LeeDepartment of Horticultural Biotechnology, Kyung Hee University, Yongin 17104, Korea.ORCID 0000-0002-9501-9008
In Sik ChungDepartment of Genetic Engineering and Graduate School of Biotechnology, Kyung Hee University, Yongin 446-701, Korea.ORCID 0000-0002-3727-1467
Kyung Hee University · KR

Funding

National Research Foundation of Korea NRF-2016R1A6A3A11933134
6 · The paper itself

Abstract

backgroundThe major determining factor of prognosis of oral squamous cell carcinoma is cervical lymph node metastasis. 6,8-Diprenylgenistein (6,8-DG), an isoflavonoid isolated from

methodsTo investigate the in vitro inhibitory effects of 6,8-DG on VEGF-A-induced lymphangiogenesis, we performed the proliferation, tube formation, and migration assay using human lymphatic microvascular endothelial cells (HLMECs). RT-PCR, Western blot, immunoprecipitation, ELISA and co-immunoprecipitation assays were used to investigate the expression levels of proteins, and mechanism of 6,8-DG. The in vivo inhibitory effects of 6,8-DG were investigated using an oral cancer sentinel lymph node (OCSLN) animal model.

results6,8-DG inhibited the proliferation, migration and tube formation of rhVEGF-A treated HLMECs. In addition, the in vivo lymphatic vessel formation stimulated by rhVEGF-A was significantly reduced by 6,8-DG. 6,8-DG inhibited the expression of VEGF-A rather than other lymphangiogenic factors in CoCl

conclusionThese data suggest that 6,8-DG inhibits VEGF-A-induced lymphangiogenesis and lymph node metastasis in vitro and in vivo. Furthermore, the inhibitory effects of 6,8-DG are probably mediated by inhibition of VEGF-A expression in cancer cells and suppression of the VEGF-A/VEGFR-2 signaling pathway in HLMEC. Thus, 6,8-DG could be novel and valuable therapeutic agents for metastasis prevention and treatment of oral cancer.

Indexed as

AnimalsAnticarcinogenic AgentsCell LineCell Line, TumorCell MovementFemaleGenisteinHumansLymphangiogenesisLymphatic MetastasisMiceMice, Inbred BALB CMouth NeoplasmsSentinel Lymph NodeVascular Endothelial Growth Factor A6,8-diprenylgenisteinAnticarcinogenic AgentsGenisteinVascular Endothelial Growth Factor A6,8-diprenylgenisteinoral cancersentinel lymph node metastasisVEGF-A-induced lymphangiogenesis

Identifiers

PMID33466636
PMCPMC7828717
OpenAlexW3119349791

What OpenQuestion holds

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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.