Evidence map›Paper›PMID 38598065›Full record

ArticleStem cell reviews and reports2024

Gastric Cancer Mesenchymal Stem Cells Trigger Endothelial Cell Functional Changes to Promote Cancer Progression.

Linjing Cui, Ting Liu, Chao Huang, Fumeng Yang, Liqi Luo, Li Sun, Yuanyuan Zhao, Deqiang Wang, Mei Wang, Yong Ji and 1 more

Abstract read
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In one paragraph

Article in Stem cell reviews and reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

11 authors at 2 institutions in 1 country.

Linjing CuiSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Ting LiuSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Chao HuangSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Fumeng YangSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Liqi LuoSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Li SunDepartment of Clinical Laboratory, Affiliated Kunshan Hospital of Jiangsu University, Suzhou, Jiangsu Province, China.
Yuanyuan ZhaoSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Deqiang WangDepartment of Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu Province, China.
Mei WangSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China.
Yong JiDepartment of Surgery, Jingjiang People's Hospital, Jingjiang, Jiangsu Province, China.
Wei ZhuSchool of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu Province, 212013, China. zhuwei@ujs.edu.cn.ORCID 0000-0002-5237-1992
Jiangsu University · CNFirst People's Hospital of Jingzhou · CN

Funding

Jiangsu Commission of Health X373National Natural Science Foundation of China 81972313National Natural Science Foundation of China 82203547Natural Science Foundation of Jiangsu Province BK20210136
6 · The paper itself

Abstract

Our previous studies have highlighted the pivotal role of gastric cancer mesenchymal stem cells (GCMSCs) in tumor initiation, progression, and metastasis. In parallel, it is well-documented that endothelial cells (ECs) undergo functional alterations in response to challenging tumor microenvironment. This study aims to elucidate whether functional changes in ECs might be induced by GCMSCs and thus influence cancer progression. Cell proliferation was assessed through CCK-8 and colony formation assays, while cell migration and invasion capabilities were evaluated by wound-healing and Transwell assays. Immunohistochemistry was employed to examine protein distribution and expression levels. Additionally, quantitative analysis of protein and mRNA expression was carried out through Western blotting and qRT-PCR respectively, with gene knockdown achieved using siRNA. Our findings revealed that GCMSCs effectively stimulate cell proliferation, migration, and angiogenesis of human umbilical vein endothelial cells (HUVECs), both in vitro and in vivo. GCMSCs promote the migration and invasion of gastric cancer cells by inducing the expression of Slit2 in HUVECs. Notably, the inhibition of phosphorylated AKT partially mitigates the aforementioned effects. In conclusion, GCMSCs may exert regulatory control over Slit2 expression in ECs via the AKT signaling pathway, thereby inducing functional changes in ECs that promote tumor progression.

Indexed as

Cell MovementCell ProliferationHuman Umbilical Vein Endothelial CellsMesenchymal Stem CellsStomach NeoplasmsAnimalsCell Line, TumorDisease ProgressionEndothelial CellsHumansIntercellular Signaling Peptides and ProteinsMiceNeovascularization, PathologicNerve Tissue ProteinsProto-Oncogene Proteins c-aktSignal TransductionIntercellular Signaling Peptides and ProteinsNerve Tissue ProteinsProto-Oncogene Proteins c-aktSlit Homolog 2 ProteinAKTCancer progressionEndothelial cellsGastric cancerMesenchymal stem cellsSlit2

Identifiers

PMID38598065
OpenAlexW4394688516

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.