Evidence map›Paper›PMID 36358584›Full record

ArticleAntioxidants (Basel, Switzerland)2022

Ishophloroglucin A Ameliorates VEGF-Induced Epithelial-Mesenchymal Transition via VEGFR2 Pathway Inhibition in Microgravity-Stimulated Human Retinal Pigment Epithelial Cells.

Myeongjoo Son, Bomi Ryu, Jun-Geon Je, You-Jin Jeon, Dae Yu Kim

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. 3D cell culture model: From ground experiment to microgravity study.Frontiers in bioengineering and biotechnology · 2023
    Review
  7. 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

5 authors at 3 institutions in 1 country.

Myeongjoo SonInha Research Institute for Aerospace Medicine, Inha University, Incheon 22212, Korea.
Bomi RyuMajor of Food Science and Nutrition, Pukyong National University, Busan 48513, Korea.ORCID 0000-0001-5797-500X
Jun-Geon JeDepartment of Marine Life Sciences, Jeju National University, Jeju 63243, Korea.
You-Jin JeonDepartment of Marine Life Sciences, Jeju National University, Jeju 63243, Korea.ORCID 0000-0003-3299-7266
Dae Yu KimInha Research Institute for Aerospace Medicine, Inha University, Incheon 22212, Korea.
Inha University · KRJeju National University · KRPukyong National University · KR

Funding

Ministry of Education 2018R1A6A1A03025523Ministry of Education 2022R1I1A1A01066045Ministry of Science and ICT 2020R1C1C1014835
6 · The paper itself

Abstract

Microgravity stimulation is associated with retinal pigment epithelial (RPE) cells that transition to mesenchymal cells (EMT), and these pathological changes cause visual impairment. Vascular endothelial growth factor (VEGF) is produced from the RPE and contributes to photoreceptor survival. However, changes in VEGF production and function under microgravity stimulation are unknown. In this study, we verified that microgravity stimulation changed the morphological characteristics of human RPE cells (ARPE19 cells) and the expression of actin cytoskeleton regulators, which are related to excessive VEGF expression. Interestingly, microgravity stimulation increased not only the production of VEGF but also the expression of EMT markers. Previously, we studied the potential of ishophloroglucin A (IPA), a phlorotannin, as an antioxidant. In silico results confirmed that IPA could structurally bind to VEGF receptor 2 (VEGFR2) among VEGFRs and inhibit the VEGF pathway. IPA significantly decreased VEGF production and EMT marker expression in microgravity-stimulated cells. It also significantly reduced excessive cell migration in VEGF-induced EMT. Overall, our findings suggested that IPA treatment decreased VEGF production and EMT marker expression in microgravity-stimulated or VEGF-treated ARPE19 cells, and this decrease in EMT could restore excessive cell migration by inhibiting the VEGF/VEGFR2 pathway. Therefore, it is a potential therapeutic candidate for angiogenesis-related eye diseases.

Indexed as

epithelial-mesenchymal transitionIshige okamuraeishophloroglucin Amicrogravityretinal pigment epitheliumvascular endothelial growth factorvascular endothelial growth factor receptor 2 signaling

Identifiers

PMID36358584
PMCPMC9686763
OpenAlexW4308602289

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.