Evidence map›Paper›PMID 24824968›Full record

ArticlePloS one2014

Activation of mesenchymal stem cells by macrophages prompts human gastric cancer growth through NF-κB pathway.

Tingting Yang, Xu Zhang, Mei Wang, Jie Zhang, Feng Huang, Jie Cai, Qiang Zhang, Fei Mao, Wei Zhu, Hui Qian and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
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  8. Article
  9. Adult Stem Cell Functioning in the Tumor Micro-Environment.International journal of molecular sciences · 2019
    Review
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  11. Review
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  13. Article
  14. Article
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  16. Article
  17. Review
  18. Review
  19. Exosomes derived from gastric cancer cells activate NF-κB pathway in macrophages to promote cancer progression.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  20. Review
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.

Tingting YangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Xu ZhangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Mei WangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Jie ZhangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Feng HuangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Jie CaiSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Qiang ZhangSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Fei MaoSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Wei ZhuSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Hui QianSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China.
Wenrong XuSchool of Medical Science and Laboratory Medicine, Jiangsu University Zhenjiang, Jiangsu, China; The Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Jiangsu University · CNAffiliated Hospital of Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence indicate that macrophages activate mesenchymal stem cells (MSCs) to acquire pro-inflammatory phenotype. However, the role of MSCs activated by macrophages in gastric cancer remains largely unknown. In this study, we found that MSCs were activated by macrophages to produce increased levels of inflammatory cytokines. Cell colony formation and transwell migration assays revealed that supernatants from the activated MSCs could promote both gastric epithelial cell and gastric cancer cell proliferation and migration. In addition, the expression of epithelial-mesenchymal transition (EMT), angiogenesis, and stemness-related genes was increased in activated MSCs. The phosphorylated forms of NF-κB, ERK and STAT3 in gastric cells were increased by active MSCs. Inhibition of NF-κB activation by PDTC blocked the effect of activated MSCs on gastric cancer cells. Co-injection of activated MSCs with gastric cancer cells could accelerate gastric cancer growth. Moreover, human peripheral blood monocytes derived macrophages also activated MSCs to prompt gastric cancer cell proliferation and migration. Taken together, our findings suggest that MSCs activated by macrophage acquire pro-inflammatory phenotype and prompt gastric cancer growth in an NF-κB-dependent manner, which provides new evidence for the modulation of MSCs by tumor microenvironment and further insight to the role of stromal cells in gastric carcinogenesis and cancer progression.

Indexed as

Analysis of VarianceAnimalsBlotting, WesternCell Line, TumorCell MovementCell ProliferationCytokinesEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansImmunohistochemistryMacrophagesMesenchymal Stem CellsMiceMice, Inbred BALB CNeovascularization, PathologicCytokinesNF-kappa B

Identifiers

PMID24824968
PMCPMC4019592
OpenAlexW2018206861

What OpenQuestion holds

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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.