NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE174796 Query DataSets for GSE174796
Status Public on Dec 01, 2021
Title S100A8/A9 induced by interaction with macrophages in esophageal squamous cell carcinoma promotes the migration and invasion of cancer cells via Akt and p38 MAPK pathways
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Tumor-associated macrophages enhance the malignant phenotypes of esophageal squamous cell carcinoma (ESCC) cells. We have previously identified several factors associated with ESCC progression using an indirect co-culture assay between ESCC cells and macrophages. Here, we newly established a direct co-culture assay between ESCC cells and macrophages which is closer to the actual cancer microenvironment than an indirect co-culture assay. To investigate the gene expression changes by co-culture with macrophages, we performed cDNA microarray analysis between mono-cultured and co-cultured ESCC cells with macrophages. We found that the expression of S100 calcium binding protein A8 and A9 (S100A8 and S100A9) was enhanced in co-cultured ESCC cells with macrophages.
S100A8 and S100A9 commonly exist stable and function as a heterodimer (S100A8/A9). S100A8/A9 is widely known as an inflammation marker. It also contributes to the enhancement of malignant phenotypes in several cancers. S100A8/A9 enhances the migration and invasion of ESCC cells by activating Akt and p38 MAPK signaling pathways. The higher expression levels of S100A8/A9 were associated with poor prognosis in ESCC patients. These results suggest that S100A8/A9 contributes to the progression of ESCC.
 
Overall design CD14 positive peripheral blood monocytes (PBMos) were selectively collected from healthy volunteers. Recombinant human macrophage colony stimulating factor (rhM-CSF) was added to induce M2 macrophages. We seeded ESCC cell line (TE-11) and direct co-cultured with the M2 macrophages. As a control, the same amount of TE-11 without macrophage was seeded and mono-cultured. We performed cDNA microarray analysis between mono-cultured TE-11 cells and co-cultured TE-11 cells with macrophages.
 
Contributor(s) Tanigawa K, Koma YI
Citation(s) 34954212
Submission date May 20, 2021
Last update date Jun 27, 2022
Contact name Satoshi Kondo
Organization name Toray Industries,Inc.
Street address 10-1 tebiro 6-chome
City Kamakura
State/province Kanagawa
ZIP/Postal code 248-8555
Country Japan
 
Platforms (1)
GPL22439 3D-Gene Human Oligo chip 25k V2.2.0
Samples (1)
GSM5328311 mono-cultured TE-11 vs direct co-cultured TE-11 with macrophages
Relations
BioProject PRJNA731538

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE174796_RAW.tar 820.0 Kb (http)(custom) TAR (of TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap