The role of the complement system in cancer

被引:464
作者
Afshar-Kharghan, Vahid [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Sect Benign Hematol, 2121 W Holcombe Blvd,Suite 7-20E, Houston, TX 77030 USA
关键词
TO-MESENCHYMAL TRANSITION; ACTIVATED PROTEIN-KINASE; MANNOSE-BINDING LECTIN; DEPENDENT CYTOTOXICITY; REGULATORY PROTEINS; ANAPHYLATOXIN C5A; IMMUNE SURVEILLANCE; C3A ANAPHYLATOXIN; EPITHELIAL-CELLS; EXPRESSED C5AR;
D O I
10.1172/JCI90962
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
In addition to being a component of innate immunity and an ancient defense mechanism against invading pathogens, complement activation also participates in the adaptive immune response, inflammation, hemostasis, embryogenesis, and organ repair and development. Activation of the complement system via classical, lectin, or alternative pathways generates anaphylatoxins (C3a and C5a) and membrane attack complex (C5b-9) and opsonizes targeted cells. Complement activation end products and their receptors mediate cell-cell interactions that regulate several biological functions in the extravascular tissue. Signaling of anaphylatoxin receptors or assembly of membrane attack complex promotes cell dedifferentiation, proliferation, and migration in addition to reducing apoptosis. As a result, complement activation in the tumor microenvironment enhances tumor growth and increases metastasis. In this Review, I discuss immune and nonimmune functions of complement proteins and the tumor-promoting effect of complement activation.
引用
收藏
页码:780 / 789
页数:10
相关论文
共 108 条
[1]
Abdelbaset-Ismail A, LEUKEMIA
[2]
Complement activation product C4d in oral and oropharyngeal squamous cell carcinoma [J].
Ajona, D. ;
Pajares, M. J. ;
Chiara, M. D. ;
Rodrigo, J. P. ;
Jantus-Lewintre, E. ;
Camps, C. ;
Suarez, C. ;
Bagan, J. V. ;
Montuenga, L. M. ;
Pio, R. .
ORAL DISEASES, 2015, 21 (07) :899-904
[3]
BAATRUP G, 1994, EUR J SURG, V160, P503
[4]
RETRACTED: TGF-β signaling regulates neuronal Clq expression and developmental synaptic refinement (Retracted Article) [J].
Bialas, Allison R. ;
Stevens, Beth .
NATURE NEUROSCIENCE, 2013, 16 (12) :1773-1782
[5]
Ascitic complement system in ovarian cancer [J].
Bjorge, L ;
Hakulinen, J ;
Vintermyr, OK ;
Jarva, H ;
Jensen, TS ;
Iversen, OE ;
Meri, S .
BRITISH JOURNAL OF CANCER, 2005, 92 (05) :895-905
[6]
PTX3 Is an Extrinsic Oncosuppressor Regulating Complement-Dependent Inflammation in Cancer [J].
Bonavita, Eduardo ;
Gentile, Stefania ;
Rubino, Marcello ;
Maina, Virginia ;
Papait, Roberto ;
Kunderfranco, Paolo ;
Greco, Carolina ;
Feruglio, Francesca ;
Molgora, Martina ;
Laface, Ilaria ;
Tartari, Silvia ;
Doni, Andrea ;
Pasqualini, Fabio ;
Barbati, Elisa ;
Basso, Gianluca ;
Galdiero, Maria Rosaria ;
Nebuloni, Manuela ;
Roncalli, Massimo ;
Colombo, Piergiuseppe ;
Laghi, Luigi ;
Lambris, John D. ;
Jaillon, Sebastien ;
Garlanda, Cecilia ;
Mantovani, Alberto .
CELL, 2015, 160 (04) :700-714
[7]
Complement activation in Glioblastoma Multiforme pathophysiology: Evidence from serum levels and presence of complement activation products in tumor tissue [J].
Bouwens, T. A. M. ;
Trouw, L. A. ;
Veerhuis, R. ;
Dirven, C. M. F. ;
Lamfers, M. L. M. ;
Al-Khawaja, H. .
JOURNAL OF NEUROIMMUNOLOGY, 2015, 278 :271-276
[8]
C1q acts in the tumour microenvironment as a cancer-promoting factor independently of complement activation [J].
Bulla, Roberta ;
Tripodo, Claudio ;
Rami, Damiano ;
Ling, Guang Sheng ;
Agostinis, Chiara ;
Guarnotta, Carla ;
Zorzet, Sonia ;
Durigutto, Paolo ;
Botto, Marina ;
Tedesco, Francesco .
NATURE COMMUNICATIONS, 2016, 7
[9]
Human colonic epithelial cells detect and respond to C5a via apically expressed C5aR through the ERK pathway [J].
Cao, Qi ;
McIsaac, Shayla M. ;
Stadnyk, Andrew W. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 302 (12) :C1731-C1740
[10]
Complement Fragment C3a Controls Mutual Cell Attraction during Collective Cell Migration [J].
Carmona-Fontaine, Carlos ;
Theveneau, Eric ;
Tzekou, Apostolia ;
Tada, Masazumi ;
Woods, Mae ;
Page, Karen M. ;
Parsons, Maddy ;
Lambris, John D. ;
Mayor, Roberto .
DEVELOPMENTAL CELL, 2011, 21 (06) :1026-1037