Interferon-α protects myeloma cell lines from dexamethasone-induced apoptosis

被引:33
|
作者
Liu, P
Oken, M
Van Ness, B
机构
[1] Univ Minnesota, Minneapolis, MN 55455 USA
[2] Virginia Piper Canc Inst, Minneapolis, MN USA
关键词
myeloma; dexamethasone; interferon-alpha; IL-6;
D O I
10.1038/sj.leu.2401334
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because of the increasing use of IFN-alpha in both induction and maintenance therapy for multiple myeloma (MM), its effect on growth and apoptosis of myeloma cells is important to consider. To investigate the role of IFN-alpha on the growth of myeloma cells, we have studied its effects on the response of interleukin 6 (IL-6)-dependent myeloma cell line (ANBL6) and IL-6-independent myeloma cell line (C2E3) in the presence of IL-6 and dexamethasone (Dex). We found that although IFN-alpha is a potent inhibitor of proliferation, it has only a minimal effect on induction of apoptosis. Moreover, we found IFN-alpha as well as IL-6 can significantly suppress dexamethasone-induced apoptosis. The suppression of apoptosis is concurrent with the induction of both AP-1 and STAT binding activity. We also found that IL-6 but not IFN-alpha up-regulates Bcl-X-L expression. However, IL-6-mediated Bcl-X-L expression is suppressed in the presence of Dex. Therefore, the expression of Bct-X-L does not account for the protection of Dex-induced apoptosis by IFN-alpha and IL-6. Taken together, our results suggest that IFN-alpha may counteract the beneficial effects of corticosteroids or perhaps other apoptosis inducing agents in the treatment of myeloma.
引用
收藏
页码:473 / 480
页数:8
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