Immune cells as anti-cancer therapeutic targets and tools

被引:21
作者
Johansson, Magnus
Tan, Tingting
de Visser, Karin E.
Coussens, Lisa M.
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[3] Netherlands Canc Inst, Dept Mol Biol, NL-1066 CX Amsterdam, Netherlands
关键词
cancer; immune cells; inflammation; innate; adative; NATURAL-KILLER-CELLS; MAST-CELLS; NK CELLS; T-CELLS; MACROPHAGE INFILTRATION; CHRONIC INFLAMMATION; DENDRITIC CELLS; CANCER; CARCINOMA; ANGIOGENESIS;
D O I
10.1002/jcb.21230
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
Chronic inflammation is a contributing factor to overall cancer risk as well as cancer promotion and progression; however, pathways regulating onset of cancer-promoting inflammatory responses are still poorly understood. Clinical data suggest that deficient anti-tumor cell-mediated immunity, in combination with enhanced pro-tumor humoral and/or innate immunity (inflammation), are significant factors influencing malignant outcome. Here, we discuss therapeutic implications from clinical data and experimental studies using de novo immune-competent mouse models of cancer development that together are revealing molecular and cellular mechanisms underlying interactions between immune cells and evolving neoplastic cells that regulate cancer outcome. Understanding the functionally significant links between adaptive and innate immunity that regulate cancer development will open new therapeutic opportunities to manipulate aspects of immunobiology and minimize lethal effects of cancer development.
引用
收藏
页码:918 / 926
页数:9
相关论文
共 59 条
[21]  
Engle SJ, 2002, CANCER RES, V62, P6362
[22]   The disease spectrum of Helicobacter pylori:: The immunopathogenesis of gastroduodenal ulcer and gastric cancer [J].
Ernst, PB ;
Gold, BD .
ANNUAL REVIEW OF MICROBIOLOGY, 2000, 54 :615-640
[23]   Inflammation and the development of pancreatic cancer [J].
Farrow, B ;
Evers, BM .
SURGICAL ONCOLOGY-OXFORD, 2002, 10 (04) :153-169
[24]   Where have all the T cells gone? Mechanisms of immune evasion by tumors [J].
Finke, J ;
Ferrone, S ;
Frey, A ;
Mufson, A ;
Ochoa, A .
IMMUNOLOGY TODAY, 1999, 20 (04) :158-160
[25]   Mechanism of immune dysfunction in cancer mediated by immature Gr-1+ myeloid cells [J].
Gabrilovich, DI ;
Velders, MP ;
Sotomayor, EM ;
Kast, WM .
JOURNAL OF IMMUNOLOGY, 2001, 166 (09) :5398-5406
[26]   Type, density, and location of immune cells within human colorectal tumors predict clinical outcome [J].
Galon, Jerom ;
Costes, Anne ;
Sanchez-Cabo, Fatima ;
Kirilovsky, Amos ;
Mlecnik, Bernhard ;
Lagorce-Pages, Christine ;
Tosolini, Marie ;
Camus, Matthieu ;
Berger, Anne ;
Wind, Philippe ;
Zinzindohoue, Franck ;
Bruneval, Patrick ;
Cugnenc, Paul-Henri ;
Trajanoski, Zlatko ;
Fridman, Wolf-Herman ;
Pages, Franck .
SCIENCE, 2006, 313 (5795) :1960-1964
[27]   An amino-bisphosphonate targets MMP-9-expressing macrophages and angiogenesis to impair cervical carcinogenesis [J].
Giraudo, E ;
Inoue, M ;
Hanahan, D .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (05) :623-633
[28]   Single-agent rituximab as first-line and maintenance treatment for patients with chronic lymphocytic leukemia or small lymphocytic lymphoma: A phase II trial of the Minnie Pearl Cancer Research Network [J].
Hainsworth, JD ;
Litchy, S ;
Barton, JH ;
Houston, GA ;
Hermann, RC ;
Bradof, JE ;
Greco, FA .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (09) :1746-1751
[29]   NK cells in innate immunity [J].
Hamerman, JA ;
Ogasawara, K ;
Lanier, LL .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (01) :29-35
[30]  
Hayakawa Y, 2002, BLOOD, V100, P1728