MAPK4 silencing in gastric cancer drives liver metastasis by positive feedback between cancer cells and macrophages

被引:16
作者
Li, Shuang [1 ,2 ,3 ,4 ]
Guo, Dongyang [1 ,2 ,3 ,4 ]
Sun, Qiang [1 ,2 ,3 ]
Zhang, Lu [1 ,2 ,3 ]
Cui, Yun [1 ,2 ,3 ]
Liu, Min [1 ,2 ,3 ]
Ma, Xixi [1 ,2 ,3 ]
Liu, Yiman [1 ,2 ,3 ]
Cui, Wenyu [1 ,2 ,3 ]
Sun, Leimin [3 ,4 ]
Teng, Lisong [3 ,5 ]
Wang, Liangjing [3 ,4 ,6 ]
Lin, Aifu [3 ,7 ]
Liu, Wei [8 ,9 ]
Zhuo, Wei [1 ,2 ,3 ,4 ]
Zhou, Tianhua [1 ,2 ,3 ,4 ,10 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Cell Biol, Hangzhou, Peoples R China
[2] Zhejiang Univ, Canc Inst, Sch Med, Affiliated Hosp 2, Hangzhou, Peoples R China
[3] Zhejiang Univ, Canc Ctr, Hangzhou, Peoples R China
[4] Zhejiang Univ, Sch Med, Inst Gastroenterol, Hangzhou, Peoples R China
[5] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Dept Oncol, Hangzhou, Peoples R China
[6] Zhejiang Univ, Sch Med, Dept Gastroenterol, Affiliated Hosp 2, Hangzhou, Peoples R China
[7] Zhejiang Univ, Coll Life Sci, Hangzhou, Peoples R China
[8] Zhejiang Univ, Sch Med, Dept Biochem, Hangzhou, Peoples R China
[9] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Cardiol, Hangzhou, Peoples R China
[10] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
基金
中国国家自然科学基金;
关键词
MIGRATION INHIBITORY FACTOR; TUMOR-ASSOCIATED MACROPHAGES; FIBROBLASTS; PROGRESSION; ACTIVATION; INFILTRATION; VITRO; MIF;
D O I
10.1038/s12276-023-00946-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver metastasis is a major cause of death in gastric cancer patients, but the underlying mechanisms are poorly understood. Through a combination of in vivo screening and transcriptome profiling followed by quantitative RT-PCR and tissue array analyses, we found that mitogen-activated protein kinase 4 (MAPK4) downregulation in gastric cancer tissues from patients is significantly associated with liver metastasis and poor prognosis. The knockdown of MAPK4 in gastric cancer cells promotes liver metastasis in orthotopic mouse models. MAPK4 depletion in gastric cancer cells induces the secretion of macrophage migration inhibitory factor (MIF) to polarize tumor-associated macrophages (TAMs) in orthotopic xenograft tumors. Moreover, TAMs activate epithelial-mesenchymal transition of gastric cancer cells to suppress MAPK4 expression, which further increases MIF secretion to polarize TAMs. Taken together, our results suggest a previously undescribed positive feedback loop between cancer cells and macrophages mediated by MAPK4 silencing that facilitates gastric cancer liver metastasis. Gastric cancer: Gene shutdown helps spread to the liverReduced activity of a key cell control gene mediates an interaction between gastric cancer cells and immune system cells called macrophages that allows the cancer to spread to the liver. Cancer cells migrating to the liver is a major cause of death for gastric cancer patients, but the mechanisms driving this process have been unclear. Researchers in China led by Tianhua Zhou and Wei Zhuo at Zhejiang University School of Medicine, Hangzhou, studied the activity of genes and their corresponding proteins in patients' cancer cells, and analyzed gene activity in mouse models of gastric cancer. They found that the gene that generates a protein called MAPK4 is significantly reduced in the cancer cells. This allows the cells to interact with macrophages, promoting their spread to the liver.
引用
收藏
页码:457 / 469
页数:13
相关论文
共 54 条
[1]   Regulation of MAPK-activated protein kinase 5 activity and subcellular localization by the atypical MAPK ERK4/MAPK4 [J].
Aberg, Espen ;
Perander, Maria ;
Johansen, Bjarne ;
Julien, Catherine ;
Meloche, Sylvain ;
Keyse, Stephen M. ;
Seternes, Ole-Morten .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (46) :35499-35510
[2]   MECHANISM OF A REACTION IN VITRO ASSOCIATED WITH DELAYED-TYPE HYPERSENSITIVITY [J].
BLOOM, BR ;
BENNETT, B .
SCIENCE, 1966, 153 (3731) :80-&
[3]  
Bruns Christiane J., 1999, Neoplasia (New York), V1, P50, DOI 10.1038/sj.neo.7900005
[4]   Cutoff Finder: A Comprehensive and Straightforward Web Application Enabling Rapid Biomarker Cutoff Optimization [J].
Budczies, Jan ;
Klauschen, Frederick ;
Sinn, Bruno V. ;
Gyoerffy, Balazs ;
Schmitt, Wolfgang D. ;
Darb-Esfahani, Silvia ;
Denkert, Carsten .
PLOS ONE, 2012, 7 (12)
[5]   Macrophage migration inhibitory factor: A regulator of innate immunity [J].
Calandra, T ;
Roger, T .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (10) :791-800
[6]   Tumor-Associated Macrophages as Major Players in the Tumor Microenvironment [J].
Chanmee, Theerawut ;
Ontong, Pawared ;
Konno, Kenjiro ;
Itano, Naoki .
CANCERS, 2014, 6 (03) :1670-1690
[7]   Tumor-recruited M2 macrophages promote gastric and breast cancer metastasis via M2 macrophage-secreted CHI3L1 protein [J].
Chen, Yulei ;
Zhang, Siyuan ;
Wang, Qizhi ;
Zhang, Xiaobo .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2017, 10 :1-13
[8]   Turning Cold into Hot: Firing up the Tumor Microenvironment [J].
Duan, Qianqian ;
Zhang, Hualing ;
Zheng, Junnian ;
Zhang, Lianjun .
TRENDS IN CANCER, 2020, 6 (07) :605-618
[9]   Blockade of MIF-CD74 Signalling on Macrophages and Dendritic Cells Restores the Antitumour Immune Response Against Metastatic Melanoma [J].
Figueiredo, Carlos R. ;
Azevedo, Ricardo A. ;
Mousdell, Sasha ;
Resende-Lara, Pedro T. ;
Ireland, Lucy ;
Santos, Almudena ;
Girola, Natalia ;
Cunha, Rodrigo L. O. R. ;
Schmid, Michael C. ;
Polonelli, Luciano ;
Travassos, Luiz R. ;
Mielgo, Ainhoa .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[10]   IL-22 produced by cancer-associated fibroblasts promotes gastric cancer cell invasion via STAT3 and ERK signaling [J].
Fukui, H. ;
Zhang, X. ;
Sun, C. ;
Hara, K. ;
Kikuchi, S. ;
Yamasaki, T. ;
Kondo, T. ;
Tomita, T. ;
Oshima, T. ;
Watari, J. ;
Imura, J. ;
Fujimori, T. ;
Sasako, M. ;
Miwa, H. .
BRITISH JOURNAL OF CANCER, 2014, 111 (04) :763-771