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NPM-ALK介导MSH2在酪氨酸238处的磷酸化,导致MSH2功能缺陷和错配修复功能丧失。

NPM-ALK mediates phosphorylation of MSH2 at tyrosine 238, creating a functional deficiency in MSH2 and the loss of mismatch repair.

作者信息

Bone K M, Wang P, Wu F, Wu C, Li L, Bacani J T, Andrew S E, Lai R

机构信息

Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Blood Cancer J. 2015 May 15;5(5):e311. doi: 10.1038/bcj.2015.35.

Abstract

The vast majority of anaplastic lymphoma kinase-positive anaplastic large cell lymphoma (ALK+ALCL) tumors express the characteristic oncogenic fusion protein NPM-ALK, which mediates tumorigenesis by exerting its constitutive tyrosine kinase activity on various substrates. We recently identified MSH2, a protein central to DNA mismatch repair (MMR), as a novel binding partner and phosphorylation substrate of NPM-ALK. Here, using liquid chromatography-mass spectrometry, we report for the first time that MSH2 is phosphorylated by NPM-ALK at a specific residue, tyrosine 238. Using GP293 cells transfected with NPM-ALK, we confirmed that the MSH2(Y238F) mutant is not tyrosine phosphorylated. Furthermore, transfection of MSH2(Y238F) into these cells substantially decreased the tyrosine phosphorylation of endogenous MSH2. Importantly, gene transfection of MSH2(Y238F) abrogated the binding of NPM-ALK with endogenous MSH2, re-established the dimerization of MSH2:MSH6 and restored the sensitivity to DNA mismatch-inducing drugs, indicative of MMR return. Parallel findings were observed in two ALK+ALCL cell lines, Karpas 299 and SUP-M2. In addition, we found that enforced expression of MSH2(Y238F) into ALK+ALCL cells alone was sufficient to induce spontaneous apoptosis. In conclusion, our findings have identified NPM-ALK-induced phosphorylation of MSH2 at Y238 as a crucial event in suppressing MMR. Our studies have provided novel insights into the mechanism by which oncogenic tyrosine kinases disrupt MMR.

摘要

绝大多数间变性淋巴瘤激酶阳性间变性大细胞淋巴瘤(ALK+ALCL)肿瘤表达特征性致癌融合蛋白NPM-ALK,其通过对各种底物发挥组成型酪氨酸激酶活性来介导肿瘤发生。我们最近鉴定出MSH2,一种DNA错配修复(MMR)的核心蛋白,作为NPM-ALK的新型结合伴侣和磷酸化底物。在此,我们使用液相色谱-质谱法首次报道MSH2在特定残基酪氨酸238处被NPM-ALK磷酸化。使用转染了NPM-ALK的GP293细胞,我们证实MSH2(Y238F)突变体未被酪氨酸磷酸化。此外,将MSH2(Y238F)转染到这些细胞中显著降低了内源性MSH2的酪氨酸磷酸化。重要的是,MSH2(Y238F)的基因转染消除了NPM-ALK与内源性MSH2的结合,重新建立了MSH2:MSH6的二聚化,并恢复了对DNA错配诱导药物的敏感性,表明MMR恢复。在两种ALK+ALCL细胞系Karpas 299和SUP-M2中观察到了类似的结果。此外,我们发现单独将MSH2(Y238F)强制表达于ALK+ALCL细胞中足以诱导自发凋亡。总之,我们的研究结果确定了NPM-ALK诱导的MSH2在Y238处的磷酸化是抑制MMR的关键事件。我们的研究为致癌酪氨酸激酶破坏MMR的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee39/4476014/03b726ad7491/bcj201535f1.jpg

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