Chronic immune activation and inflammation as the cause of malignancy

被引:401
作者
O'Byrne, KJ
Dalgleish, A [1 ]
机构
[1] Univ Leicester, Dept Oncol, London SW17 0RR, England
[2] Univ London St Georges Hosp, Sch Med, Div Oncol, London SW17 0RR, England
关键词
cell mediated immunity; humoral immunity; angiogenesis; cancer;
D O I
10.1054/bjoc.2001.1943
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several chronic infections known to be associated with malignancy have established oncogenic properties. However the existence of chronic inflammatory conditions that do not have an established infective cause and are associated with the development of tumours strongly suggests that the inflammatory process itself provides the prerequisite environment for the development of malignancy. This environment includes upregulation of mediators of the inflammatory response such as cyclo-oxygenase (COX)-2 leading to the production of inflammatory cytokines and prostaglandins which themselves may suppress cell mediated immune responses and promote angiogenesis. These factors may also impact on cell growth and survival signalling pathways resulting in induction of cell proliferation and inhibition of apoptosis. Furthermore, chronic inflammation may lead to the production of reactive oxygen species and metabolites such as malondialdehyde within the affected cells that may in turn induce DNA damage and mutations and, as a result, be carcinogenic. Here it is proposed that the conditions provided by a chronic inflammatory environment are so essential for the progression of the neoplastic process that therapeutic intervention aimed at inhibiting inflammation, reducing angiogenesis and stimulating cell mediated immune responses may have a major role in reducing the incidence of common cancers. (C) 2001 Cancer Research Campaign.
引用
收藏
页码:473 / 483
页数:11
相关论文
共 171 条
[1]  
AKER K, 2001, BRIT J CANCER, V84, P965
[2]  
Al-Saleh W, 1998, J PATHOL, V184, P283, DOI 10.1002/(SICI)1096-9896(199803)184:3<283::AID-PATH25>3.0.CO
[3]  
2-K
[4]   Ultraviolet B (UVB)-induced COX-2 expression in murine skin: An immunohistochemical study [J].
Athar, M ;
An, KP ;
Morel, KD ;
Kim, AL ;
Aszterbaum, M ;
Longley, J ;
Epstein, EH ;
Bickers, DR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (04) :1042-1047
[5]   ROLE OF SCHISTOSOMIASIS IN HUMAN BLADDER-CANCER - EVIDENCE OF ASSOCIATION, ETIOLOGIC FACTORS, AND BASIC MECHANISMS OF CARCINOGENESIS [J].
BADAWI, AF ;
MOSTAFA, MH ;
PROBERT, A ;
OCONNOR, PJ .
EUROPEAN JOURNAL OF CANCER PREVENTION, 1995, 4 (01) :45-59
[6]   Involvement of regulatory and catalytic subunits of phosphoinositide 3-kinase in NF-κB activation [J].
Béraud, C ;
Henzel, WJ ;
Baeuerle, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (02) :429-434
[7]   Effects of angiogenesis inhibitors on multistage carcinogenesis in mice [J].
Bergers, G ;
Javaherian, K ;
Lo, KM ;
Folkman, J ;
Hanahan, D .
SCIENCE, 1999, 284 (5415) :808-812
[8]  
BielefeldtOhmann H, 1996, J PATHOL, V178, P369, DOI 10.1002/(SICI)1096-9896(199604)178:4<369::AID-PATH460>3.0.CO
[9]  
2-8
[10]   Detection of Epstein-Barr virus in invasive breast cancers [J].
Bonnet, M ;
Guinebretiere, JM ;
Kremmer, E ;
Grunewald, V ;
Benhamou, E ;
Contesso, G ;
Joab, I .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (16) :1376-1381