Complement inhibition in cancer therapy

被引:114
作者
Pio, Ruben [1 ,2 ]
Ajona, Daniel [1 ]
Lambris, John D. [3 ]
机构
[1] Ctr Appl Med Res CIMA, Div Oncol, Pamplona, Spain
[2] Univ Navarra, Sch Sci, Dept Biochem & Genet, E-31080 Pamplona, Spain
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA
关键词
Complement system; Cancer therapy; Tumor microenvironment; Inflammation; Immunosuppression; Angiogenesis; ACTIVATED PROTEIN-KINASE; SMOOTH-MUSCLE-CELLS; COLORECTAL-CANCER; SIGNALING PATHWAY; TUMOR-CELLS; ALTERNATIVE PATHWAY; C5A RECEPTOR; FACTOR-H; IMMUNE SURVEILLANCE; REGULATORY PROTEINS;
D O I
10.1016/j.smim.2013.04.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
For decades, complement has been recognized as an effector arm of the immune system that contributes to the destruction of tumor cells. In fact, many therapeutic strategies have been proposed that are based on the intensification of complement-mediated responses against tumors. However, recent studies have challenged this paradigm by demonstrating a tumor-promoting role for complement. Cancer cells seem to be able to establish a convenient balance between complement activation and inhibition, taking advantage of complement initiation without suffering its deleterious effects. Complement activation may support chronic inflammation, promote an immunosuppressive microenvironment, induce angiogenesis, and activate cancer-related signaling pathways. In this context, inhibition of complement activation would be a therapeutic option for treating cancer. This concept is relatively new and deserves closer attention. In this article, we summarize the mechanisms of complement activation on cancer cells, the cancer-promoting effect of complement initiation, and the rationale behind the use of complement inhibition as a therapeutic strategy against cancer. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:54 / 64
页数:11
相关论文
共 147 条
[31]   Overexpression of RGC-32 in colon cancer and other tumors [J].
Fosbrink, M ;
Cudrici, C ;
Niculescu, F ;
Badea, TC ;
David, S ;
Shamsuddin, A ;
Shin, ML ;
Rus, H .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2005, 78 (02) :116-122
[32]   C1 AND C-4 ABNORMALITIES IN CHRONIC LYMPHOCYTIC-LEUKEMIA AND THEIR SIGNIFICANCE [J].
FUST, G ;
MISZLAY, Z ;
CZINK, E ;
VARGA, L ;
PALOCZI, K ;
SZEGEDI, G ;
HOLLAN, SR .
IMMUNOLOGY LETTERS, 1987, 14 (03) :255-259
[33]   Cancer resistance to complement-dependent cytotoxicity (CDC): Problem-oriented research and development [J].
Gancz, Dana ;
Fishelson, Zvi .
MOLECULAR IMMUNOLOGY, 2009, 46 (14) :2794-2800
[34]   Complement activation on human neuroblastoma cell lines in vitro: Route of activation and expression of functional complement regulatory proteins [J].
Gasque, P ;
Thomas, A ;
Fontaine, M ;
Morgan, BP .
JOURNAL OF NEUROIMMUNOLOGY, 1996, 66 (1-2) :29-40
[35]   Angiogenesis in colorectal cancer: Prognostic and therapeutic implications [J].
Giatromanolaki, Alexandra ;
Sivridis, Efthimios ;
Koukourakis, Michael I. .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2006, 29 (04) :408-417
[36]   Fibrotic mechanisms in idiopathic rapidly progressive glomerulonephritis:: The role of TGF-β1 and C5b-9 [J].
Gionanlis, Lazaros ;
Alexopoulos, Efstathios ;
Papagianni, Aikaterini ;
Leontsini, Maria ;
Memmos, Dimitrios .
RENAL FAILURE, 2008, 30 (02) :239-246
[37]   Complement activation induces dysregulation of angiogenic factors and causes fetal rejection and growth restriction [J].
Girardi, Guillermina ;
Yarilin, Dmitry ;
Thurman, Joshua M. ;
Holers, V. Michael ;
Salmon, Jane E. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (09) :2165-2175
[38]   Therapeutic targets and biomarkers identified in cancer choline phospholipid metabolism [J].
Glunde, Kristine ;
Serkova, Natalie J. .
PHARMACOGENOMICS, 2006, 7 (07) :1109-1123
[39]  
Gminski J., 1992, Revue Roumaine de Medecine Interne, V30, P39
[40]   Immune evasion of tumor cells using membrane-bound complement regulatory proteins [J].
Gorter, A ;
Meri, S .
IMMUNOLOGY TODAY, 1999, 20 (12) :576-582