Proinflammatory Cytokines in Breast Cancer: Mechanisms of Action and Potential Targets for Therapeutics

被引:3
|
作者
Goldberg, Jodi E. [2 ]
Schwertfeger, Kathryn L. [1 ]
机构
[1] Univ Minnesota, Dept Lab Med & Pathol, Masonic Canc Ctr, Minneapolis, MN 55455 USA
[2] Hamline Univ, Dept Biol, St Paul, MN 55104 USA
关键词
Breast cancer; cytokine; inflammation; interleukin-1beta; interleukin-6; tumor necrosis factor-alpha; TUMOR-NECROSIS-FACTOR; INTERLEUKIN-1 RECEPTOR ANTAGONIST; KAPPA-B ACTIVATION; LYMPHOBLASTOID CELL-LINE; TNF-ALPHA; HUMAN LYMPHOTOXIN; GROWTH-FACTOR; RHEUMATOID-ARTHRITIS; TRANSGENIC MICE; IL-1; RECEPTOR;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inflammation within the tumor microenvironment correlates with increased invasiveness and poor prognosis in many types of cancer, including breast cancer. The cytokines interleukin-6 (IL-6), tumor necrosis factor alpha (TNF alpha) and interleukin-1 beta (IL-1 beta) are critical mediators of the inflammatory response. Numerous studies have also linked these cytokines to breast cancer progression. As a result, the mechanisms by which these cytokines promote breast cancer have been recently explored using both in vitro and in vivo models. The results from these studies have led to speculation regarding the possible usefulness of targeting these cytokines in breast cancer patients. This review summarizes the most recent studies pertaining to the mechanisms by which proinflammatory cytokines promote breast cancer. Furthermore, the possibilities of targeting these inflammatory mediators in breast cancer patients using inhibitors that are currently being used in the clinic for other inflammatory conditions are discussed. Understanding both the mechanisms by which inflammatory mediators promote breast cancer and the effectiveness of anti-inflammatory drugs in treating breast cancer will lead to novel therapeutic regimens to treat this devastating disease.
引用
收藏
页码:1133 / 1146
页数:14
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