Tumor-associated macrophages regulate gastric cancer cell invasion and metastasis through TGFβ2/NF-κB/Kindlin-2 axis

被引:44
|
作者
Wang, Zhu [1 ,2 ]
Yang, Yang [1 ,2 ]
Cui, Yancheng [1 ,2 ,3 ,4 ]
Wang, Chao [1 ,2 ]
Lai, Zhiyong [1 ,2 ]
Li, Yansen [1 ,2 ]
Zhang, Wei [1 ,2 ]
Mustonen, Harri [3 ,4 ]
Puolakkainen, Pauli [3 ,4 ]
Ye, Yingjiang [1 ,2 ]
Jiang, Kewei [1 ,2 ]
Shen, Zhanlong [1 ,2 ]
Wang, Shan [1 ]
机构
[1] Peking Univ, Dept Gastroenterol Surg, Peoples Hosp, 11 Xizhimen South St, Beijing 100044, Peoples R China
[2] Peking Univ, Lab Surg Oncol, Beijing Key Lab Colorectal Canc Diag & Treatment, Peoples Hosp, Beijing 100044, Peoples R China
[3] Helsinki Univ Cent Hosp, Dept Surg, Helsinki 00290, Finland
[4] Univ Helsinki, FIN-00290 Helsinki, Finland
基金
中国国家自然科学基金;
关键词
Gastric cancer; tumor-associated macrophage; Kindlin-2; invasion and metastasis; NF-KAPPA-B; KINDLIN-2; ACTIVATION; ADENOCARCINOMA; PROMOTES; PROGRESSION; EXPRESSION;
D O I
10.21147/j.issn.1000-9604.2020.01.09
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Recent studies have shown that tumor-associated macrophages (TAMs) play an important role in cancer invasion and metastasis. Our previous studies have reported that TAMs promote the invasion and metastasis of gastric cancer (GC) cells through the Kindlin-2 pathway. However, the mechanism needs to be clarified. Methods: THP-1 monocytes were induced by PMA/interleukin (IL)-4/IL-13 to establish an efficient TAM model in vitro and M2 macrophages were isolated via flow cytometry. A dual luciferase reporter system and chromatin immunoprecipitation (ChIP) assay were used to investigate the mechanism of transforming growth factor beta 2 (TGF beta 2) regulating Kindlin-2 expression. Immunohistochemistry was used to study the relationships among TAM infiltration in human GC tissues, Kindlin-2 protein expression, clinicopathological parameters and prognosis in human GC tissues. A nude mouse oncogenesis model was used to verify the invasion and metastasis mechanisms in vivo. Results: We found that Kindlin-2 expression was upregulated at both mRNA and protein levels in GC cells cocultured with TAMs, associated with higher invasion rate. Kindlin-2 knockdown reduced the invasion rate of GC cells under coculture condition. TGF beta 2 secreted by TAMs regulated the expression of Kindlin-2 through the transcription factor NF-kappa B. TAMs thus participated in the progression of GC through the TGF beta 2/NF-kappa B/Kindlin-2 axis. Kindlin-2 expression and TAM infiltration were significantly positively correlated with TNM stage, and patients with high Kindlin-2 expression had significantly poorer overall survival than patients with low Kindlin-2 expression. Furthermore, Kindlin-2 promoted the invasion of GC cells in vivo. Conclusions: This study elucidates the mechanism of TAMs participating in GC cell invasion and metastasis through the TGF beta 2/NF-kappa B/Kindlin-2 axis, providing a possibility for new treatment options and approaches.
引用
收藏
页码:72 / +
页数:20
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