摘要
背景:弥漫性大B细胞淋巴瘤(DLBCL)约三分之一为难治性或复发性。新的治疗方法包括B细胞受体抑制剂(BCR)吴。蛋白激酶CK2促进实体瘤和血液病患者的生存、增殖和应激反应,并促进“非癌基因成瘾”表型。该激酶是否调节bcr si格宁是DLBCL的一个合适的药理靶点,目前尚不清楚。目的:建立CK2是否控制DLBCL细胞存活和bcr信号传导,以检测其联合作用。CK2抑制剂CX-4945和Bcr阻断剂伊布鲁替尼和福沙替尼对DLBCL细胞的细胞毒性比单药更有效,并对BC下游信号分子的变化进行了调查r对CK2的抑制作用。 方法:用CX-49 45、Fostamatinib或IrBurib处理GC和ABC-DLBCL细胞。BCR信号转导的细胞内Ca~(++)检测及标志的磷酸化Aling分子。流式细胞术、Western blot和MTT法检测细胞存活率。 结果:CK2抑制CX-4945可导致DLBCL细胞死亡.CX-4945在BCR作用下,AKT磷酸化和胞内钙动员受到抑制。CK2抑制剂与SYK抑制剂福斯塔尼或BTK抑制剂Ibrutinib均可诱导DLBCL细胞死亡。cx-4945在gc和abc dlbcl亚型以及“双击”dlbcl cell lin中同样有效。Spain 西班牙. 结论:BCR下游CK2在控制不同DLBCL亚型细胞生长的生存通路中起着重要作用。同时,Cx-4945在Wi组合中的使用TH BCR信号传导阻滞剂可作为DLBCL的一种新的合理的治疗方法。
关键词: 凋亡,CK2,弥漫性大B细胞淋巴瘤,治疗策略,B细胞受体,信号传导。
图形摘要
Current Cancer Drug Targets
Title:CX-4945, a Selective Inhibitor of Casein Kinase 2, Synergizes with B Cell Receptor Signaling Inhibitors in Inducing Diffuse Large B Cell Lymphoma Cell Death
Volume: 18 Issue: 6
关键词: 凋亡,CK2,弥漫性大B细胞淋巴瘤,治疗策略,B细胞受体,信号传导。
摘要: Background: Approximately one third of Diffuse Large B cell Lymphomas (DLBCL) are refractory or relapse. Novel therapeutic approaches under scrutiny include inhibitors of B-cell receptor (BCR) signaling. Protein kinase CK2 propels survival, proliferation and stress response in solid and hematologic malignancies and promotes a “non-oncogene addiction” phenotype. Whether this kinase regulates BCR signaling, being a suitable pharmacological target in DLBCL, is unknown.
Objective: The objective was to establish if CK2 controls DLBCL cell survival and the BCR signaling, to check if the combination of CK2 inhibitor CX-4945 and BCR blockers Ibrutinib and Fostamatinib is more effectively cytotoxic for DLBCL cells than the single agents and to survey the changes in signaling molecules downstream BCR upon CK2 inhibition.
Method: A panel of GC and ABC DLBCL cells was treated with CX-4945 and Fostamatinib or Ibrutinib. BCR signaling was assayed by intracellular Ca++ measurement and looking at the phosphorylation of signaling molecules. The effects on cell survival were assessed by flow cytometry, western blot and MTT assays.
Results: CK2 inhibition with CX-4945 causes DLBCL cell death. CX-4945 impaired AKT phosphorylation and intracellular Ca++ mobilization upon BCR engagement. The CK2 inhibitor acted synergistically with either the SYK inhibitor Fostamatinib or the BTK inhibitor Ibrutinib in inducing DLBCL cell death. CX-4945 was equally effective in GC and ABC DLBCL subtypes as well as in “double hit” DLBCL cell lines.
Conclusion: These findings suggest a role for CK2 downstream of the BCR in controlling survival pathways crucial for cell growth of different DLBCL subtypes. Also, the use of CX-4945 in combination with BCR signaling blockers could represent a novel rational therapeutic approach in the DLBCL.
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CX-4945, a Selective Inhibitor of Casein Kinase 2, Synergizes with B Cell Receptor Signaling Inhibitors in Inducing Diffuse Large B Cell Lymphoma Cell Death, Current Cancer Drug Targets 2018; 18 (6) . https://dx.doi.org/10.2174/1568009617666170427110450
DOI https://dx.doi.org/10.2174/1568009617666170427110450 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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