NCAM- and FGF-2-mediated FGFR1 signaling in the tumor microenvironment of esophageal cancer regulates the survival and migration of tumor-associated macrophages and cancer cells

被引:63
作者
Takase, Nobuhisa [1 ,2 ]
Koma, Yu-ichiro [1 ]
Urakawa, Naoki [1 ,2 ]
Nishio, Mari [1 ]
Arai, Noriaki [1 ]
Akiyama, Hiroaki [1 ]
Shigeoka, Manabu [1 ]
Kakeji, Yoshihiro [2 ]
Yokozaki, Hiroshi [1 ]
机构
[1] Kobe Univ, Grad Sch Med, Div Pathol, Dept Pathol,Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, Div Gastrointestinal Surg, Dept Surg,Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan
基金
日本学术振兴会;
关键词
NCAM; FGF-2; FGFR1; Esophageal cancer; Macrophage; Tumor microenvironment; FIBROBLAST-GROWTH-FACTOR; MOLECULE N-CAM; ADHESION MOLECULE; FACTOR RECEPTOR; PROGNOSTIC BIOMARKER; ACTIVATION; PROGRESSION; LUNG; EXPRESSION; CARCINOMA;
D O I
10.1016/j.canlet.2016.06.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor-associated macrophages (TAMs) have important roles in the angiogenesis and tumor immuno-suppression of various cancers, including esophageal squamous cell carcinomas (ESCCs). To elucidate the roles of TAMs in ESCCs, we compared the gene expression profiles between human peripheral blood monocyte-derived macrophage-like cells (Macrophage_Ls) and Macrophage_Ls stimulated with conditioned medium of the TE series human ESCC cell line (TECM) (TAM_Ls) using cDNA microarray analysis. Among the highly expressed genes in TAM_Ls, we focused on neural cell adhesion molecule (NCAM). NCAM knockdown in TAM_Ls revealed a significant decrease of migration and survival via a suppression of PI3K-Akt and fibroblast growth factor receptor I (FGFR1) signaling. Stimulation by TECM up-regulated the level of FGFR1 in Macrophage_Ls. Recombinant human fibroblast growth factor-2 (rhFGF-2) promoted the migration and survival of TAM_Ls and TE-cells through FGFR1 signaling. Our immunohistochemical analysis of 70 surgically resected ESCC samples revealed that the up-regulated FGF-2 in stromal cells, including macrophages, was associated with more aggressive phenotypes and a high number of infiltrating M2 macrophages. These findings may indicate a novel role of NCAM- and FGF-2-mediated FGFRI signaling in the tumor microenvironment of ESCCs. (C) 2016 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:47 / 58
页数:12
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