Division of Hematology, Department of Internal Medicine, The Ohio State University, 460 OSUCCC, 410 West 12th Avenue, Columbus, OH, 43210, USA.
Department of Veterinary Biosciences, The Ohio State University, Columbus, OH, USA.
J Hematol Oncol. 2021 Jan 15;14(1):17. doi: 10.1186/s13045-021-01032-2.
Exportin 1 (XPO1/CRM1) is a key mediator of nuclear export with relevance to multiple cancers, including chronic lymphocytic leukemia (CLL). Whole exome sequencing has identified hot-spot somatic XPO1 point mutations which we found to disrupt highly conserved biophysical interactions in the NES-binding groove, conferring novel cargo-binding abilities and forcing cellular mis-localization of critical regulators. However, the pathogenic role played by change-in-function XPO1 mutations in CLL is not fully understood.
We performed a large, multi-center retrospective analysis of CLL cases (N = 1286) to correlate nonsynonymous mutations in XPO1 (predominantly E571K or E571G; n = 72) with genetic and epigenetic features contributing to the overall outcomes in these patients. We then established a mouse model with over-expression of wildtype (wt) or mutant (E571K or E571G) XPO1 restricted to the B cell compartment (Eµ-XPO1). Eµ-XPO1 mice were then crossed with the Eµ-TCL1 CLL mouse model. Lastly, we determined crystal structures of XPO1 (wt or E571K) bound to several selective inhibitors of nuclear export (SINE) molecules (KPT-185, KPT-330/Selinexor, and KPT-8602/Eltanexor).
We report that nonsynonymous mutations in XPO1 associate with high risk genetic and epigenetic features and accelerated CLL progression. Using the newly-generated Eµ-XPO1 mouse model, we found that constitutive B-cell over-expression of wt or mutant XPO1 could affect development of a CLL-like disease in aged mice. Furthermore, concurrent B-cell expression of XPO1 with E571K or E571G mutations and TCL1 accelerated the rate of leukemogenesis relative to that of Eµ-TCL1 mice. Lastly, crystal structures of E571 or E571K-XPO1 bound to SINEs, including Selinexor, are highly similar, suggesting that the activity of this class of compounds will not be affected by XPO1 mutations at E571 in patients with CLL.
These findings indicate that mutations in XPO1 at E571 can drive leukemogenesis by priming the pre-neoplastic lymphocytes for acquisition of additional genetic and epigenetic abnormalities that collectively result in neoplastic transformation.
Exportin 1(XPO1/CRM1)是核输出的关键介质,与包括慢性淋巴细胞白血病(CLL)在内的多种癌症有关。全外显子组测序已鉴定出热点体细胞 XPO1 点突变,我们发现这些突变破坏了 NES 结合槽中的高度保守的生物物理相互作用,赋予了新的货物结合能力,并迫使关键调节剂发生细胞内定位错误。然而,XPO1 突变导致 CLL 发病的作用机制尚不完全清楚。
我们对 1286 例 CLL 病例进行了大型、多中心回顾性分析,以将 XPO1 中的非同义突变(主要为 E571K 或 E571G;n=72)与遗传和表观遗传特征相关联,这些特征有助于这些患者的总体结局。然后,我们建立了一个仅在 B 细胞区室中过表达野生型(wt)或突变型(E571K 或 E571G)XPO1 的小鼠模型(Eµ-XPO1)。Eµ-XPO1 小鼠随后与 Eµ-TCL1 CLL 小鼠模型杂交。最后,我们确定了 XPO1(wt 或 E571K)与几种选择性核输出抑制剂(SINE)分子(KPT-185、KPT-330/Selinexor 和 KPT-8602/Eltanexor)结合的晶体结构。
我们报告说,XPO1 中的非同义突变与高风险遗传和表观遗传特征以及 CLL 的加速进展相关。使用新生成的 Eµ-XPO1 小鼠模型,我们发现 wt 或突变型 XPO1 的组成性 B 细胞过表达可影响老年小鼠中 CLL 样疾病的发展。此外,与 Eµ-TCL1 小鼠相比,B 细胞同时表达 XPO1 的 E571K 或 E571G 突变和 TCL1 加速了白血病的发生。最后,E571 或 E571K-XPO1 与 SINE 结合的晶体结构,包括 Selinexor,高度相似,表明在 CLL 患者中,XPO1 中的 E571 突变不会影响此类化合物的活性。
这些发现表明,XPO1 中的 E571 突变可通过启动前肿瘤淋巴细胞获得额外的遗传和表观遗传异常,从而驱动白血病发生,这些异常共同导致肿瘤转化。