Xu Zhen-Shu, Zhang Ju-Shun, Zhang Jing-Yan, Wu Shun-Quan, Xiong Dong-Lian, Chen Hui-Jun, Chen Zhi-Zhe, Zhan Rong
Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematology, Fujian Medical University Union Hospital, Fuzhou, P.R. China.
Oncol Rep. 2015 Apr;33(4):1609-14. doi: 10.3892/or.2015.3762. Epub 2015 Jan 29.
NOTCH1 mutations occur in approximately 10% of patients with chronic lymphocytic leukemia (CLL). However, the relationship between the genetic aberrations and tumor cell drug resistance or disease progression remains unclear. Frameshift deletions were detected by gene sequencing in the NOTCH1 PEST domain in three naive CLL patients. These mutations were associated with chromosomal abnormalities including trisomy 12 or 13q deletion. Of note, one of the patients developed Richter's transformation during FCR treatment. Immunofluorescent and western blot analyses revealed a markedly higher intracellular domain of NOTCH (ICN) expression in the mutated cells compared with their unmutated counterparts and normal CD19+ B lymphocytes (P<0.01 and P<0.001, respectively). In addition, strong DNA-κB binding activities were observed in the mutant cells by gel shift assays. RT-PCR analysis revealed elevated RelA mRNA expression in the mutant cells, while RelB levels were variable. Reduced levels of RelA and RelB mRNA were observed in unmutated CLL and normal B cells. Compared to unmutated CLL and normal B cells, increased apoptosis occurred in the mutant cells in the presence of GSI (ICN inhibitor) and PDTC (NF-κB inhibitor), particularly under the synergistic effects of the two drugs (P=0.03). Moreover, IKKα and IKKβ, the active components in the NF-κB pathway, were markedly inhibited following prolonged treatment with GSI and PDTC. These results suggested that NOTCH1 mutations constitutively activate the NF-κB signaling pathway in CLL, which is likely related to ICN overexpression, indicating NOTCH1 and NF-κB as potential therapeutic targets in the treatment of CLL.
NOTCH1突变发生在约10%的慢性淋巴细胞白血病(CLL)患者中。然而,基因畸变与肿瘤细胞耐药性或疾病进展之间的关系仍不清楚。通过基因测序在3例初治CLL患者的NOTCH1 PEST结构域中检测到移码缺失。这些突变与包括12号染色体三体或13q缺失在内的染色体异常相关。值得注意的是,其中1例患者在FCR治疗期间发生了Richter转化。免疫荧光和蛋白质印迹分析显示,与未突变细胞和正常CD19+B淋巴细胞相比,突变细胞中NOTCH(ICN)的细胞内结构域表达明显更高(分别为P<0.01和P<0.001)。此外,通过凝胶迁移试验在突变细胞中观察到较强的DNA-κB结合活性。RT-PCR分析显示突变细胞中RelA mRNA表达升高,而RelB水平则有所不同。在未突变的CLL和正常B细胞中观察到RelA和RelB mRNA水平降低。与未突变的CLL和正常B细胞相比,在存在GSI(ICN抑制剂)和PDTC(NF-κB抑制剂)的情况下,突变细胞中凋亡增加,特别是在两种药物的协同作用下(P=0.03)。此外,在长期用GSI和PDTC处理后,NF-κB途径中的活性成分IKKα和IKKβ受到明显抑制。这些结果表明,NOTCH1突变在CLL中组成性激活NF-κB信号通路,这可能与ICN过表达有关,表明NOTCH1和NF-κB是治疗CLL的潜在治疗靶点。