Is nuclear factor kappa-B the missing link between inflammation, cancer and alteration in hepatic drug metabolism in patients with cancer?

被引:31
作者
Assenat, E
Gerbal-Chaloin, S
Maurel, P
Vilarem, MJ
Pascussi, JM [1 ]
机构
[1] CHRU Montpellier, Hop St Eloi, Serv Hepatogastroenterol, F-34295 Montpellier, France
[2] INSERM, U632, F-34293 Montpellier, France
[3] Univ Montpellier I, F-34000 Montpellier, France
关键词
cancer; inflammation; cytochrome P450; drug metabolism;
D O I
10.1016/j.ejca.2006.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the last few years, several studies have provided a causal link between constitutive activation of nuclear factor kappa-B (NF-kappa B) and the initiation and development of cancer. More recently, it appears that a cancer-induced inflammatory response may be an important factor in the inter-individual variability of the response to and toxic effects of cancer chemotherapy, as well as in the alteration of drug metabolism enzyme expression in patients. The relationships between chronic inflammation (or infection), cancer and drug metabolism are many: chronic infections lead to inflammation, inflammation may lead to cancer, cancer usually leads to an inflammatory syndrome, and inflammation alters the expression of drug metabolising enzymes and thus of the efficiency of cancer chemotherapy This review focuses on the functional consequences of NF-kappa B activation during oncogenesis and on the expression of the major cytochrome P450s (CYP) involved in anticancer therapies. Finally, the potential role of NF-kappa B as the missing link between inflammation, cancer and alteration in hepatic drug metabolism in patients with cancer is discussed. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:785 / 792
页数:8
相关论文
共 94 条
[71]   NF-κB functions as a tumour promoter in inflammation-associated cancer [J].
Pikarsky, E ;
Porat, RM ;
Stein, I ;
Abramovitch, R ;
Amit, S ;
Kasem, S ;
Gutkovich-Pyest, E ;
Urieli-Shoval, S ;
Galun, E ;
Ben-Neriah, Y .
NATURE, 2004, 431 (7007) :461-466
[72]   Repression of inflammatory responses in the absence of DNA binding by the glucocorticoid receptor [J].
Reichardt, HM ;
Tuckermann, JP ;
Göttlicher, M ;
Vujic, M ;
Weih, F ;
Angel, P ;
Herrlich, P ;
Schütz, G .
EMBO JOURNAL, 2001, 20 (24) :7168-7173
[73]   An immunocytochemical study of pituitary cells of the Senegalese sole, Solea senegalensis (Kaup 1858) [J].
Rendon, C ;
Rodriguez-Gomez, FJ ;
Muñoz-Cueto, JA ;
Piñuela, C ;
Sarasquete, C .
HISTOCHEMICAL JOURNAL, 1997, 29 (11-12) :813-822
[74]   Clinical update: proteasome inhibitors in hematologic malignancies [J].
Richardson, P .
CANCER TREATMENT REVIEWS, 2003, 29 :33-39
[75]   Hepatic cytochrome P450 3A drug metabolism is reduced in cancer patients who have an acute-phase response [J].
Rivory, LP ;
Slaviero, KA ;
Clarke, SJ .
BRITISH JOURNAL OF CANCER, 2002, 87 (03) :277-280
[76]   Nuclear factor κB is activated in macrophages and epithelial cells of inflamed intestinal mucosa [J].
Rogler, G ;
Brand, K ;
Vogl, D ;
Page, S ;
Hofmeister, R ;
Andus, T ;
Knuechel, R ;
Baeuerle, PA ;
Schölmerich, J ;
Gross, V .
GASTROENTEROLOGY, 1998, 115 (02) :357-369
[77]  
ROSIN MP, 1994, CANCER RES, V54, pS1929
[78]  
Roy P, 1999, DRUG METAB DISPOS, V27, P655
[79]   Nuclear receptors orchestrate detoxification pathways [J].
Roy-Chowdhury, J ;
Locker, J ;
Roy-Chowdhury, N .
DEVELOPMENTAL CELL, 2003, 4 (05) :607-608
[80]  
SCHEINMAN RI, 1995, MOL CELL BIOL, V15, P943