Macrophages in pancreatic cancer: An immunometabolic perspective

被引:45
作者
Yang, Jian [1 ]
Li, Yongzheng [1 ]
Sun, Zhaowei [2 ]
Zhan, Hanxiang [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Gen Surg, Div Pancreat Surg, Jinan 250012, Shandong, Peoples R China
[2] Qingdao Univ, Dept Hepatobiliary & Pancreat Surg, Affiliated Hosp, Qingdao 266003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic cancer; Macrophage; Tumor microenvironment; Metabolism; Obesity; TUMOR-ASSOCIATED MACROPHAGES; NF-KAPPA-B; EPITHELIAL-MESENCHYMAL TRANSITION; SIGNALING PATHWAYS; NECROSIS-FACTOR; ADIPOSE-TISSUE; INFLAMMATORY CYTOKINES; THERAPEUTIC STRATEGIES; DUCTAL ADENOCARCINOMA; IMMUNE SUPPRESSION;
D O I
10.1016/j.canlet.2020.10.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As one of the most fatal gastrointestinal cancers, pancreatic cancer (PC) has a long-term survival rate that has shown limited improvement during recent decades and remains dismal. The poor prognosis is attributed to challenges in early detection, low opportunity for radical resection and resistance to chemotherapy and radiation. Macrophages are one of the most abundant infiltrating immune cells in PC stroma, and they can crosstalk with cancer cells, adipocytes and other stromal cells to modulate metabolism, inflammation and immune status, create an immunosuppressive tumor microenvironment (TME), and ultimately facilitate tumor initiation and progression. In this review, we summarize recent advances in our understanding of macrophage origin, distribution and polarization, as well as provide a thorough review of the role macrophages in PC carcinogenesis and development, as well as the underlying molecular mechanism. Additionally, we investigated macrophage targets in preclinical and clinical trials to evaluate their potential therapeutic value in PC.
引用
收藏
页码:188 / 200
页数:13
相关论文
共 187 条
[31]   Tissue-resident macrophages: then and now [J].
Davies, Luke C. ;
Taylor, Philip R. .
IMMUNOLOGY, 2015, 144 (04) :541-548
[32]   Tissue-resident macrophages [J].
Davies, Luke C. ;
Jenkins, Stephen J. ;
Allen, Judith E. ;
Taylor, Philip R. .
NATURE IMMUNOLOGY, 2013, 14 (10) :986-995
[33]   High-Fat, High-Calorie Diet Promotes Early Pancreatic Neoplasia in the Conditional KrasG12D Mouse Model [J].
Dawson, David W. ;
Hertzer, Kathleen ;
Moro, Aune ;
Donald, Graham ;
Chang, Hui-Hua ;
Go, Vay Liang ;
Pandol, Steven J. ;
Lugea, Aurelia ;
Gukovskaya, Anna S. ;
Li, Gang ;
Hines, Oscar J. ;
Rozengurt, Enrique ;
Eibl, Guido .
CANCER PREVENTION RESEARCH, 2013, 6 (10) :1064-1073
[34]   Macrophage Regulation of Tumor Responses to Anticancer Therapies [J].
De Palma, Michele ;
Lewis, Claire E. .
CANCER CELL, 2013, 23 (03) :277-286
[35]   Vascular endothelial growth factor receptor 2 mediates macrophage infiltration into orthotopic pancreatic tumors in mice [J].
Dineen, Sean P. ;
Lynn, Kristi D. ;
Holloway, Shane E. ;
Miller, Andrew F. ;
Sullivan, James P. ;
Shames, David S. ;
Beck, Adam W. ;
Barnett, Carlton C. ;
Fleming, Jason B. ;
Brekken, Rolf A. .
CANCER RESEARCH, 2008, 68 (11) :4340-4346
[36]   Langerhans Cells - The Macrophage in Dendritic Cell Clothing [J].
Doebel, Thomas ;
Voisin, Benjamin ;
Nagao, Keisuke .
TRENDS IN IMMUNOLOGY, 2017, 38 (11) :817-828
[37]   VEGF-A/VEGFR-2 Signaling Plays an Important Role for the Motility of Pancreas Cancer Cells [J].
Doi, Yosuke ;
Yashiro, Masakazu ;
Yamada, Nobuya ;
Amano, Ryosuke ;
Noda, Satoru ;
Hirakawa, Kosei .
ANNALS OF SURGICAL ONCOLOGY, 2012, 19 (08) :2733-2743
[38]   Epithelial-mesenchymal transition and inflammation at the site of the primary tumor [J].
Dominguez, Charli ;
David, Justin M. ;
Palena, Claudia .
SEMINARS IN CANCER BIOLOGY, 2017, 47 :177-184
[39]  
Du Cheyne C., 2019, ANAT HISTOL EMBRYOL
[40]  
Du Cheyne C., 2019, ANATOMIA HISTOLOGIA