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一种新型非肽 14-3-3 抑制剂诱导对伊马替尼敏感或耐药的慢性髓系白血病细胞凋亡。

A new nonpeptidic inhibitor of 14-3-3 induces apoptotic cell death in chronic myeloid leukemia sensitive or resistant to imatinib.

机构信息

Dipartimento di Ematologia e Scienze Oncologiche Lorenzo e Ariosto Seràgnoli, Policlinico S. Orsola, Bologna, Italy.

出版信息

J Pharmacol Exp Ther. 2011 Mar;336(3):596-604. doi: 10.1124/jpet.110.172536. Epub 2010 Nov 1.

Abstract

Resistance of chronic myeloid leukemia (CML) to tyrosine kinase inhibitor imatinib mesylate (IM) is most often due to point mutations in the Bcr-Abl fusion gene. T315I mutation (resulting in substitution of Ile for a Thr residue at the "gatekeeper" position 315) raises particular concern, because it also provides resistance to second-generation kinase inhibitors already approved for clinical use (nilotinib and dasatinib). Much effort is therefore focused on alternative molecular-based strategies. Previous studies proved that binding to 14-3-3 scaffolding proteins leads to cytoplasmic compartmentalization and suppression of proapoptotic and antiproliferative signals associated with Bcr-Abl protein kinase, hence contributing to leukemic clone expansion. Here we investigated the effect of 14-3-3 inhibition disruption on hematopoietic cells expressing the IM-sensitive wild type Bcr-Abl and the IM-resistant T315I mutation. Using a virtual screening protocol and docking simulations, we identified a nonpeptidic inhibitor of 14-3-3, named BV02, that exhibits a remarkable cytotoxicity against both cell types. c-Abl release from 14-3-3σ, promoting its relocation to nuclear compartment (where it triggers transcription of p73-dependent proapoptotic genes) and to mitochondrial membranes (where it induces the loss of mitochondrial transmembrane potential) combined with c-Abl enhanced association with caspase 9 (a critical step of sequential caspase activation further contributing to c-Abl pro-apoptotic function) has a prominent role in the effect of BV02 on Bcr-Abl-expressing cells. In conclusion, BV02 may be considered as a treatment option for CML and, in particular, for more advanced phases of the disease that developed IM resistance as a consequence of Bcr-Abl point mutations.

摘要

慢性髓性白血病 (CML) 对甲磺酸伊马替尼 (IM) 的耐药性通常是由于 Bcr-Abl 融合基因的点突变引起的。T315I 突变(导致第 315 位“门控”位置的 Thr 残基被 Ile 取代)引起了特别的关注,因为它还对已经批准用于临床的第二代激酶抑制剂(尼洛替尼和达沙替尼)产生耐药性。因此,人们非常关注替代的基于分子的策略。先前的研究证明,与 14-3-3 支架蛋白结合会导致细胞质区室化,并抑制与 Bcr-Abl 蛋白激酶相关的促凋亡和抗增殖信号,从而有助于白血病克隆的扩增。在这里,我们研究了 14-3-3 抑制破坏对表达 IM 敏感野生型 Bcr-Abl 和 IM 耐药 T315I 突变的造血细胞的影响。使用虚拟筛选方案和对接模拟,我们鉴定出一种非肽 14-3-3 抑制剂,命名为 BV02,它对两种细胞类型都表现出显著的细胞毒性。c-Abl 从 14-3-3σ 释放,促进其向核区室(在那里它触发 p73 依赖性促凋亡基因的转录)和线粒体膜(在那里它诱导线粒体跨膜电位的丧失)的重新定位,与 c-Abl 与 caspase 9 的增强关联(caspase 级联激活的关键步骤,进一步促进 c-Abl 的促凋亡功能)在 BV02 对表达 Bcr-Abl 的细胞的作用中起着重要作用。总之,BV02 可以被认为是 CML 的一种治疗选择,特别是对于因 Bcr-Abl 点突变而发展出 IM 耐药性的疾病的更晚期阶段。

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