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
[21]   'Why do tumour cells glycolyse?': From glycolysis through citrate to lipogenesis [J].
Costello, LC ;
Franklin, RB .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2005, 280 (1-2) :1-8
[22]   Expression of a functional c5a receptor in regenerating hepatocytes and its involvement in a proliferative signaling pathway in rat [J].
Daveau, M ;
Benard, M ;
Scotte, M ;
Schouft, MT ;
Hiron, M ;
Francois, A ;
Salier, JP ;
Fontaine, M .
JOURNAL OF IMMUNOLOGY, 2004, 173 (05) :3418-3424
[23]   C1 inhibitor, a multi-functional serine protease inhibitor [J].
Davis, Alvin E., III ;
Lu, Fengxin ;
Mejia, Pedro .
THROMBOSIS AND HAEMOSTASIS, 2010, 104 (05) :886-893
[24]   Paradoxical roles of the immune system during cancer development [J].
de Visser, KE ;
Eichten, A ;
Coussens, LM .
NATURE REVIEWS CANCER, 2006, 6 (01) :24-37
[25]   Immune Therapy for Cancer [J].
Dougan, Michael ;
Dranoff, Glenn .
ANNUAL REVIEW OF IMMUNOLOGY, 2009, 27 :83-117
[26]   Expression of galectin-3 in the tumor immune response in colon cancer [J].
Dumont, Patrick ;
Berton, Alix ;
Nagy, Nathalie ;
Sandras, Flavienne ;
Tinton, Sandrine ;
Demetter, Pieter ;
Mascart, Francoise ;
Allaoui, Abdelmounaaim ;
Decaestecker, Christine ;
Salmon, Isabelle .
LABORATORY INVESTIGATION, 2008, 88 (08) :896-906
[27]   Enhanced expression of the complement regulatory protein CD55 predicts a poor prognosis in colorectal cancer patients [J].
Durrant, LG ;
Chapman, MA ;
Buckley, DJ ;
Spendlove, I ;
Robins, RA ;
Armitage, NC .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2003, 52 (10) :638-642
[28]   Novel Therapeutic Inhibitors of the c-Met Signaling Pathway in Cancer [J].
Eder, Joseph Paul ;
Woude, George F. Vande ;
Boerner, Scott A. ;
LoRusso, Patricia M. .
CLINICAL CANCER RESEARCH, 2009, 15 (07) :2207-2214
[29]   Complement-dependent enhancement of CD8+ T cell immunity to lymphocytic choriomeningitis virus infection in decay-accelerating factor-deficient mice [J].
Fang, Chongyun ;
Miwa, Takashi ;
Shen, Hao ;
Song, Wen-Chao .
JOURNAL OF IMMUNOLOGY, 2007, 179 (05) :3178-3186
[30]   Obstacles to cancer immunotherapy: expression of membrane complement regulatory proteins (mCRPs) in tumors [J].
Fishelson, Z ;
Donin, N ;
Zell, S ;
Schultz, S ;
Kirschfink, M .
MOLECULAR IMMUNOLOGY, 2003, 40 (2-4) :109-123