Evidence map›Paper›PMID 28849193›Full record

ArticleInternational journal of molecular medicine2017

Fluid shear stress regulates vascular remodeling via VEGFR-3 activation, although independently of its ligand, VEGF-C, in the uterus during pregnancy.

Yang-Gyu Park, Jawun Choi, Hye-Kang Jung, In Kyu Song, Yongwhan Shin, Sang-Youel Park, Jae-Won Seol

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Regulation of VEGFR3 signaling in lymphatic endothelial cells.Frontiers in cell and developmental biology · 2025
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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

7 authors at 1 institution in 1 country.

Yang-Gyu ParkBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
Jawun ChoiBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
Hye-Kang JungBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
In Kyu SongBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
Yongwhan ShinAuckland International College, Auckland 0600, New Zealand.
Sang-Youel ParkBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
Jae-Won SeolBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jwonbuk 54596, Republic of Korea.
Jeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early pregnancy is characterized by an increase in the blood volume of the uterus for embryonic development, thereby exerting fluid shear stress (FSS) on the vascular walls. The uterus experiences vascular remodeling to accommodate the increased blood flow. The blood flow‑induced FSS elevates the expression of vascular endothelial growth factors (VEGFs) and their receptors, and regulates vascular remodeling through the activation of VEGF receptor-3 (VEGFR-3). However, the mechanisms responsible for FSS-induced VEGFR-3 expression in the uterus during pregnancy are unclear. In this study, we demonstrate that vascular remodeling in the uterus during pregnancy is regulated by FSS-induced VEGFR-3 expression. We examined the association between VEGFR-3 and FSS through in vivo and in vitro experiments. In vivo experiments revealed VEGFR-3 expression in the CD31-positive region of the uterus of pregnant mice; VEGF-C (ligand for VEGFR‑3) was undetected in the uterus. These results confirmed that VEGFR-3 expression in the endometrium is independent of its ligand. In vitro studies experiments revealed that FSS induced morphological changes and increased VEGFR-3 expression in human uterine microvascular endothelial cells. Thus, VEGFR-3 activation by FSS is associated with vascular remodeling to allow increased blood flow in the uterus during pregnancy.

Indexed as

Mechanotransduction, CellularAnimalsEmbryo, MammalianEmbryonic DevelopmentEndothelium, VascularFemaleGene Expression RegulationHumansLigandsMiceMice, Inbred C57BLPregnancyRheologyStress, MechanicalUterusVascular Endothelial Growth Factor CLigandsVascular Endothelial Growth Factor Cvascular endothelial growth factor C, mouseVascular Endothelial Growth Factor Receptor-3

Identifiers

PMID28849193
PMCPMC5593466
OpenAlexW2749835268

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.