Combination with γ-secretase inhibitor prolongs treatment efficacy of BRAF inhibitor in BRAF-mutated melanoma cells

被引:8
作者
Zhu, Guannan [1 ,2 ]
Yi, Xiuli [1 ]
Haferkamp, Sebastian [3 ]
Hesbacher, Sonja [2 ]
Li, Chunying [1 ]
Goebeler, Matthias [2 ]
Gao, Tianwen [1 ]
Houben, Roland [2 ]
Schrama, David [2 ]
机构
[1] Fourth Mil Med Univ, Dept Dermatol, Xijing Hosp, Xian 710032, Peoples R China
[2] Univ Hosp Wurzburg, Dept Dermatol, Wurzburg, Germany
[3] Univ Regensburg, Dept Dermatol, D-93053 Regensburg, Germany
基金
中国国家自然科学基金;
关键词
Melanoma; Notch; Senescence; BRAF inhibition; ONCOGENE-INDUCED SENESCENCE; N-CADHERIN; METASTATIC MELANOMA; NOTCH; MUTATIONS; PATHWAY; SURVIVAL; SUPPRESSION; PROGRESSION; RESISTANCE;
D O I
10.1016/j.canlet.2016.03.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncogenic triggering of the MAPK pathway in melanocytes results in senescence, and senescence escape is considered as one critical step for melanocytic transformation. In melanoma, induction of a senescent like state by BRAF-inhibitors (BRAFi) in a fraction of treated cells - instead of killing - contributes to the repression of tumor growth, but may also provide a source for relapse. Here, we demonstrate that NOTCH activation in melanocytes is not only growth-promoting but it also protects these cells against oncogene-induced senescence. In turn, treatment of melanoma cells with an inhibitor of the NOTCH-activating enzyme gamma-secretase led to induction of a senescent-like status in a fraction of the cells but overall achieved only a moderate inhibition of melanoma cell growth. However, combination of gamma-secretase inhibitor (GSI) with BRAFi markedly increased the treatment efficacy particularly in long-term culture. Moreover, even melanoma cells starting to regrow after continuous BRAFi treatment - the major problem of BRAFi therapy in patients - can still be affected by the combination treatment. Thus, combining GSI with BRAFi increases the therapeutic efficacy by, at least partially, prolonging the senescent-like state of treated cells. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
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