Evidence map›Paper›PMID 36613819›Full record

ArticleInternational journal of molecular sciences2022

TNF-α Secreted from Macrophages Increases the Expression of Prometastatic Integrin αV in Gastric Cancer.

Mi-Aie Hwang, Misun Won, Joo-Young Im, Mi-Jung Kang, Dae-Hyuk Kweon, Bo-Kyung Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Recent advances in spasmolytic polypeptide expressing metaplasia research.World journal of gastrointestinal oncology · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. The Functions of SARS-CoV-2 Receptors in Diabetes-Related Severe COVID-19.International journal of molecular sciences · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. 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

6 authors at 2 institutions in 1 country.

Mi-Aie HwangPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.ORCID 0000-0002-0361-9293
Misun WonPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.
Joo-Young ImPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.ORCID 0000-0001-6923-8189
Mi-Jung KangPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.
Dae-Hyuk KweonDepartment of Integrative Biotechnology, College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Bo-Kyung KimPersonalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.ORCID 0000-0003-0863-3008
Korea Research Institute of Bioscience and Biotechnology · KRSungkyunkwan University · KR

Funding

Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program KGM5192221National Research Foundation NRF-2019R1A2C1087492
6 · The paper itself

Abstract

The tumor microenvironment comprising blood vessels, fibroblasts, immune cells, and the extracellular matrix surrounding cancer cells, has recently been targeted for research in cancer therapy. We aimed to investigate the effect of macrophages on the invasive ability of gastric cancer cells, and studied their potential mechanism. In transcriptome analysis, integrin αV was identified as a gene increased in AGS cells cocultured with RAW264.7 cells. AGS cells cocultured with RAW264.7 cells displayed increased adhesion to the extracellular matrix and greater invasiveness compared with AGS cells cultured alone. This increased invasion of AGS cells cocultured with RAW264.7 cells was inhibited by integrin αV knockdown. In addition, the increase in integrin αV expression induced by tumor necrosis factor-α (TNF-α) or by coculture with RAW264.7 cells was inhibited by TNF receptor 1 (TNFR1) knockdown. The increase in integrin αV expression induced by TNF-α was inhibited by both Mitogen-activated protein kinase (MEK) inhibitor and VGLL1 S84 peptide treatment. Finally, transcription of integrin αV was shown to be regulated through the binding of VGLL1 and TEAD4 to the promoter of integrin αV. In conclusion, our study demonstrated that TNFR1-ERK-VGLL1 signaling activated by TNF-α secreted from RAW264.7 cells increased integrin αV expression, thereby increasing the adhesion and invasive ability of gastric cancer cells.

Indexed as

Stomach NeoplasmsTumor Necrosis Factor-alphaDNA-Binding ProteinsHumansIntegrin alphaVMacrophagesReceptors, Tumor Necrosis Factor, Type ITEA Domain Transcription FactorsTranscription FactorsTumor MicroenvironmentDNA-Binding ProteinsIntegrin alphaVReceptors, Tumor Necrosis Factor, Type ITEAD4 protein, humanTEA Domain Transcription FactorsTranscription FactorsTumor Necrosis Factor-alphaVGLL1 protein, humangastric cancerintegrin αVmacrophageTNF-α

Identifiers

PMID36613819
PMCPMC9820470
OpenAlexW4313260604

What Socratic holds

Textmetadata
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 Socratic graph.