Evidence map›Paper›PMID 30662670›Full record

ArticleAmerican journal of translational research2018

Interaction between BMSCs and EPCs promotes IUA angiogenesis via modulating PI3K/Akt/Cox2 axis.

Jing Yu, Lijuan Jiang, Yutao Gao, Qijian Sun, Beibei Liu, Yong Hu, Xuesong Han

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  19. The Effect of Mitomycin C on Reducing Endometrial Fibrosis for Intrauterine Adhesion.Medical science monitor : international medical journal of experimental and clinical research · 2020
    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

7 authors at 2 institutions in 1 country.

Jing YuDepartment of Gynecology, The Third Affiliated Hospital of Kunming Medical University, Cancer Hospital of Yunnan Province Kunming, China.
Lijuan JiangDepartment of Scientific Research and Education, The First Affiliated Hospital of Yunnan University of Traditional Chinese Medicine Kunming, Yunnan, China.
Yutao GaoDepartment of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.
Qijian SunDepartment of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.
Beibei LiuDepartment of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.
Yong HuDepartment of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.
Xuesong HanDepartment of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.
Kunming Medical University · CNYunnan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intrauterine adhesion (IUA) is a common disease among women after uterus operation. BMSCs are commonly used as a therapeutic agent for IUA treatment, but the underlying mechanism is not fully delineated. Here we showed that BMSCs co-cultured with EPCs promotes proliferative ability and decreases apoptosis ratio of BMSCs and EPCs. In addition, BMSCs promote the differentiation of EPCs into vascular endothelial cells, and BMSCs derived epithelial cells are also induced by EPCs. We also found that the levels of Collagen Type I, vascular endothelial growth factor (VEGF), granulocyte-macrophage colony stimulating factor (GM-CSF) and bone morphogenetic protein (BMP-2) are significantly increased in the co-culturing system comparing to those of the BMSCs or EPCs alone group. Of note, PI3K/Akt/Cox2 axis is activated in the co-culturing system and LY294002 abrogates the co-culturing system's effects on cell proliferation, apoptosis and cytokines secretion, which are reversed by synergistically overexpressing Cox2. In conclusion, our in vitro experiments proved that the interaction of BMSCs and EPCs might promote angiogenesis and alleviate IUA pathogenesis by regulating PI3K/Akt/Cox2 axis mediated modulation of cell apoptosis, proliferation, differentiation and angiogenesis-associated cytokines secretion.

Indexed as

angiogenesisBMSCsEPCsIUA

Identifiers

PMID30662670
PMCPMC6325499
OpenAlexW2981496193

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.