Hypothesis: the antitumor activities of statins may be mediated by IL-18

被引:15
作者
Takahashi, Hideo Kohka
Weitz-Schmidt, Gabriele
Iwagaki, Hiromi
Yoshino, Tadashi
Tanaka, Noriaki
Nishibori, Masahiro
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pharmacol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Gastroenterol Surg Transplant & Surg Oncol, Okayama 7008558, Japan
[3] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pathol, Okayama 7008558, Japan
[4] Novartis Biomed Res, Basel, Switzerland
关键词
statin; cancer;
D O I
10.1189/jlb.0406245
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Statins, which inhibit 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) reductase, are thought to reduce the risk of cancer through the inhibition of Ras farnesylation and serum lipid level. A pleiotropic proinflammatory cytokine, interleukin-18 (IL-18), is reported to exhibit significant antitumor activities through the activation of cytotoxic T lymphocytes and natural killer cells and the inhibition of angiogenesis. Previously, we found that pravastatin, fluvastatin, and simvastatin induced the production of IL-18 in human monocytes. The addition of mevalonate abolished the IL-18 production induced by pravastatin, fluvastatin, and simvastatin, indicating that the IL-18 production might be a result of the inhibition of HMG-CoA reductase. We present a new hypothesis that the production of IL-18 might play roles in the action of statins on cancer. J. Leukoc. Biol. 80: 215-216; 2006.
引用
收藏
页码:215 / 216
页数:2
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