Bruserud Øystein, Selheim Frode, Hernandez-Valladares Maria, Reikvam Håkon
Acute Leukemia Research Group, Department of Clinical Science, University of Bergen, 5021 Bergen, Norway.
Section for Hematology, Department of Medicine, Haukeland University Hospital, 5007 Bergen, Norway.
Biomolecules. 2025 Jan 24;15(2):175. doi: 10.3390/biom15020175.
Exportin 1 is responsible for the export of hundreds of proteins, several RNA species and ribosomal components from the nucleus to the cytoplasm. Several transported proteins are important for regulation of cell proliferation and survival both in normal and malignant cells. We review the biological importance and the possibility of therapeutic targeting of Exportin 1 in acute myeloid leukemia (AML). Exportin 1 levels can be increased in human primary AML cells, and even exportin inhibition as monotherapy seems to have an antileukemic effect. The results from Phase I/II studies also suggest that exportin inhibition can be combined with conventional chemotherapy, including intensive induction and consolidation therapy possibly followed by allogeneic stem cell transplantation as well as AML-stabilizing therapy in elderly/unfit patients with hypomethylating agents. However, the risk of severe toxicity needs to be further evaluated; hematological toxicity is common together with constitutional side effects, electrolyte disturbances, and gastrointestinal toxicity. A recent randomized study of intensive chemotherapy with and without the Exportin inhibitor selinexor in elderly patients showed reduced survival in the selinexor arm; this was due to a high frequency of relapse and severe infections during neutropenia. Experimental studies suggest that Exportin 1 inhibition can be combined with other forms of targeted therapy. Thus, Exportin 1 inhibition should still be regarded as a promising strategy for AML treatment, but future studies should focus on the risk of toxicity when combined with conventional chemotherapy, especially in elderly/unfit patients, combinations with targeted therapies, identification of patient subsets (AML is a heterogeneous disease) with high susceptibility, and the possible use of less toxic next-generation Exportin 1 inhibitors.
输出蛋白1负责将数百种蛋白质、多种RNA种类和核糖体成分从细胞核输出到细胞质。几种被转运的蛋白质对于正常细胞和恶性细胞中细胞增殖和存活的调节都很重要。我们综述了输出蛋白1在急性髓系白血病(AML)中的生物学重要性以及治疗靶向的可能性。在人类原发性AML细胞中,输出蛋白1的水平可能会升高,甚至单药抑制输出蛋白似乎也有抗白血病作用。I/II期研究结果还表明,抑制输出蛋白可以与传统化疗联合使用,包括强化诱导和巩固治疗,之后可能进行异基因干细胞移植,以及对老年/身体状况不佳的患者使用低甲基化药物进行AML稳定治疗。然而,严重毒性的风险需要进一步评估;血液学毒性很常见,同时伴有全身副作用、电解质紊乱和胃肠道毒性。最近一项针对老年患者进行的有或无输出蛋白抑制剂塞利尼索的强化化疗随机研究表明,塞利尼索组的生存率降低;这是由于复发频率高以及中性粒细胞减少期间严重感染所致。实验研究表明,抑制输出蛋白1可以与其他形式的靶向治疗联合使用。因此,抑制输出蛋白1仍应被视为AML治疗的一种有前景的策略,但未来的研究应关注与传统化疗联合使用时的毒性风险,尤其是在老年/身体状况不佳的患者中,与靶向治疗的联合使用,确定高易感性的患者亚组(AML是一种异质性疾病),以及使用毒性较小的下一代输出蛋白1抑制剂的可能性。