Hu Y, Song W, Cirstea D, Lu D, Munshi N C, Anderson K C
LeBow Institute for Myeloma Therapeutics and Jerome Lipper Center for Multiple Myeloma Research, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Leukemia. 2015 Feb;29(2):474-82. doi: 10.1038/leu.2014.202. Epub 2014 Jun 25.
Here we report that targeting casein kinase 1-α1 (CSNK1α1) is a potential novel treatment strategy in multiple myeloma (MM) therapy distinct from proteasome inhibition. CSNK1α1 is expressed in all the tested MM cell lines and patient MM cells, and is not altered during bortezomib-triggered cytotoxicity. Inhibition of CSNK1α1 kinase activity in MM cells with targeted therapy D4476 or small hairpin RNAs triggers cell G0/G1-phase arrest, prolonged G2/M phase and apoptosis. D4476 also induced cytotoxicity in bortezomib-resistant MM cells and enhanced bortezomib-triggered cytotoxicity. CSNK1α1 signaling pathways include CDKN1B, P53 and FADD; gene signatures involved included interferon-α, tumor necrosis factor-α and LIN9. In addition, reduction of Csnk1α1 prevents cMYC/KRAS12V transformation of BaF3 cells independent of interleukin-3. Impartially, reducing Csnk1α1 prevented development of cMYC/KRAS12V-induced plasmacytomas in mice, suggesting that CSNK1α1 may be involved in MM initiation and progression. Our data suggest that targeting CSNK1α1, alone or combined with bortezomib, is a potential novel therapeutic strategy in MM. Moreover, inhibition of CSNK1α1 may prevent the progression of monoclonal gammopathy of undetermined significance to MM.
在此我们报告,靶向酪蛋白激酶1-α1(CSNK1α1)是多发性骨髓瘤(MM)治疗中一种有潜力的新型治疗策略,不同于蛋白酶体抑制。CSNK1α1在所有测试的MM细胞系和患者MM细胞中均有表达,且在硼替佐米引发的细胞毒性过程中未发生改变。用靶向疗法D4476或小发夹RNA抑制MM细胞中的CSNK1α1激酶活性会触发细胞G0/G1期阻滞、延长G2/M期并诱导凋亡。D4476还可诱导硼替佐米耐药的MM细胞产生细胞毒性,并增强硼替佐米引发的细胞毒性。CSNK1α1信号通路包括CDKN1B、P53和FADD;涉及的基因特征包括干扰素-α、肿瘤坏死因子-α和LIN9。此外,降低Csnk1α1可独立于白细胞介素-3阻止BaF3细胞发生cMYC/KRAS12V转化。公平地说,降低Csnk1α1可阻止小鼠中cMYC/KRAS12V诱导的浆细胞瘤的发展,这表明CSNK1α1可能参与MM的起始和进展。我们的数据表明,单独或与硼替佐米联合靶向CSNK1α1是MM中一种有潜力的新型治疗策略。此外,抑制CSNK1α1可能会阻止意义未明的单克隆丙种球蛋白病进展为MM。