Back to Search Start Over

Distribution and prognostic impact of M1 macrophage on esophageal squamous cell carcinoma.

Authors :
Jiang, Chen Hao
Liang, Wei Hua
Li, Fan Ping
Xie, Yu Fang
Yuan, Xin
Zhang, Hai Jun
Li, Man
Li, Jiang Fen
Zhang, An Zhi
Yang, Lan
Liu, Chun Xia
Pang, Li Juan
Li, Feng
Hu, Jian Ming
Source :
Carcinogenesis. Apr2021, Vol. 42 Issue 4, p537-545. 9p.
Publication Year :
2021

Abstract

Macrophages are a double-edged sword with potential cancer-promoting and anticancer effects. Controversy remains regarding the effect of macrophages, especially M1 macrophages, on tumor promotion and suppression. We aimed to investigate the role of M1 macrophages in the occurrence and progression of esophageal squamous cell carcinoma (ESCC). Analyzing the data in Gene Expression Omnibus database by the CIBERSORT algorithm found that M1 macrophages were one of the important components of many immune cells in ESCCs, and the increase in their number was obviously negatively correlated with tumor T staging. This result was verified by our experimental data: the density of CD68/HLA-DR double-stained M1 macrophages in ESCC tumor nest and tumor stroma was significantly higher than that in cancer-adjacent normal (CAN) tissues. The density of M1 macrophages in ESCC tumor nest was negatively correlated with the patient's lymph node metastasis and clinical stage (P < 0.05), and the negative tendency was more obvious for M1 macrophages in ESCC tumor stroma (P < 0.001). Exposure to M1 macrophage-conditioned medium inhibited ESCC cell migration and invasion ability significantly (P < 0.05). Moreover, the increased M1 macrophage density in ESCC tumor stroma correlated positively with good prognosis of ESCC. M1 macrophages were involved in inhibiting ESCC cell migration and invasion, which could serve as a good prognostic factor in patients with ESCC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01433334
Volume :
42
Issue :
4
Database :
Academic Search Index
Journal :
Carcinogenesis
Publication Type :
Academic Journal
Accession number :
150595463
Full Text :
https://doi.org/10.1093/carcin/bgaa128