Interferon: Current Status and Future Prospects in Cancer Therapy

被引:65
作者
Wang, Ben X. [2 ]
Rahbar, Ramtin [2 ]
Fish, Eleanor N. [1 ,2 ]
机构
[1] Univ Hlth Network, Toronto Gen Res Inst, Div Cell & Mol Biol, Toronto, ON M5G 2M1, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON, Canada
关键词
CHRONIC MYELOGENOUS LEUKEMIA; CHRONIC MYELOID-LEUKEMIA; RENAL-CELL CARCINOMA; COOPERATIVE-ONCOLOGY-GROUP; PHASE-III TRIAL; ACQUIRED-IMMUNODEFICIENCY-SYNDROME; COMPLETE CYTOGENETIC RESPONDERS; HIGH-DOSE INTERLEUKIN-2; HIGH-RISK MELANOMA; ADJUVANT THERAPY;
D O I
10.1089/jir.2010.0158
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
Type I interferons (IFNs) exhibit antiproliferative activity and apoptotic effects, and regulate an immune response by activating multiple cells types, including dendritic cells, cytotoxic T cells, and natural killer cells. Most recently, a report in the literature identified dysfunctional induction of a type I IFN response in cancer stem cells-specifically, breast cancer-initiating cells, implicating this defect in progression to breast cancer. Indeed, accumulating evidence suggests that cancer stem cells/cancer-initiating cells are prevalent in leukemias and solid tumors, are resistant to chemotherapy and radiation therapy, and therefore likely contribute to tumor recurrence. IFN-beta treatment of human glioma xenografts leads to disruption of the vascular niche of glioma stem cells, in further support of a potential therapeutic effect of IFN treatment in limiting cancer stem cells. The implications are that restoring an IFN response, or enhancing an IFN response, may invoke a reduction, or elimination of both cancer stem cells and tumor cells. In this review, the clinical application of type I IFNs, mainly IFN-alpha s, will be reviewed.
引用
收藏
页码:545 / 552
页数:8
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