Evidence map›Paper›PMID 39134872›Full record

ArticleIn vitro cellular & developmental biology. Animal2024

The role of MDM2 in angiogenesis: implications for endothelial tip cell formation.

Yi Yi, Lina Suo, Haixiu Ma, Ronghua Ma, Jing Zhao, Shaoqian Zhai, Haiyan Wang, Zhanhai Su

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yi YiDepartment of Basic Medicine Science, Qinghai University Medical College, Xining, 810001, China.
Lina SuoDepartment of Basic Medicine Science, Qinghai University Medical College, Xining, 810001, China.
Haixiu MaResearch Center for High Altitude Medicine, Key Laboratory for High Altitude Medicine, Ministry of Education, Qinghai University, 16# Kunlun Road, Xining, 810016, Qinghai, China.
Ronghua MaResearch Center for High Altitude Medicine, Key Laboratory for High Altitude Medicine, Ministry of Education, Qinghai University, 16# Kunlun Road, Xining, 810016, Qinghai, China.
Jing ZhaoResearch Center for High Altitude Medicine, Key Laboratory for High Altitude Medicine, Ministry of Education, Qinghai University, 16# Kunlun Road, Xining, 810016, Qinghai, China.
Shaoqian ZhaiDepartment of Basic Medicine Science, Qinghai University Medical College, Xining, 810001, China.
Haiyan WangDepartment of Basic Medicine Science, Qinghai University Medical College, Xining, 810001, China. wanghaiyan@qhu.edu.cn.
Zhanhai SuDepartment of Basic Medicine Science, Qinghai University Medical College, Xining, 810001, China. suzhanhai@qhu.edu.cn.ORCID http://orcid.org/0000-0003-4871-3651

Funding

Natural Science Foundation of China 32360242Qinghai Province Applied Basic Research Fund 2023-ZJ-932M
6 · The paper itself

Abstract

In the present study, we examined the role of MDM2 in the angiogenesis process and its potential association with the sprouting of endothelial tip cells. To address this, we performed hypoxia-treated gastric cancer cells (HGC-27) to quantitative RT-PCR and Western blot analysis to measure the levels of MDM2 and VEGF-A mRNA and protein expression. Subsequently, we employed siRNA to disrupt MDM2 expression, followed by hypoxia treatment. The expression levels of MDM2 and VEGF-A mRNA and protein were subsequently reassessed. Additionally, ELISA was utilized to quantify the secretion levels of VEGF-A in each experimental group. A conditioned medium derived from HGC-27 cells treated with different agents was employed to assess its influence on the formation of EA.hy926 endothelial tip cells, using various techniques including Transwell plates migration assays, wound healing experiments, vascular formation assays, scanning electron microscopy, and immunofluorescence staining. These findings demonstrated that the in vitro knockdown of MDM2 in the conditioned medium exhibited significant inhibitory effects on endothelial cell migration, wound healing, and vascular formation. Additionally, the intervention led to a reduction in the presence of CD34

Indexed as

Cell MovementEndothelial CellsNeovascularization, PathologicProto-Oncogene Proteins c-mdm2Vascular Endothelial Growth Factor AAngiogenesisCell HypoxiaCell Line, TumorCulture Media, ConditionedHumansNeovascularization, PhysiologicPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionWound HealingCulture Media, ConditionedMDM2 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mdm2Vascular Endothelial Growth Factor AAngiogenesisDLL4Gastrci CancerPI3K/AKTTip cell

Identifiers

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.