Targeting nuclear import and export in hematological malignancies

被引:58
作者
Nachmias, Boaz [1 ]
Schimmer, Aaron D. [1 ]
机构
[1] Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
关键词
ACUTE MYELOID-LEUKEMIA; B-CELL LYMPHOMA; FACTOR-KAPPA-B; SELECTIVE INHIBITORS; MULTIPLE-MYELOMA; TOPOISOMERASE-II; XPO1; INHIBITION; ORAL SELINEXOR; CLINICAL-TRIAL; LEPTOMYCIN B;
D O I
10.1038/s41375-020-0958-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The transport of proteins across the nuclear membrane is a highly regulated process, essential for the cell function. This transport is actively mediated by members of the karyopherin family, termed importins, or exportins, depending on the direction of transport. These proteins play an active part in tumorigenesis, through aberrant localization of their cargoes, which include oncogenes, tumor-suppressor genes and mediators of key signal transduction pathways. Overexpression of importins and exportins is reported in many malignancies, with implications in cell growth and viability, differentiation, drug resistance, and tumor microenvironment. Given their broad significance across tumors and pathways, much effort is being put to develop specific inhibitors as a novel anticancer therapeutics. Already, selinexor, a specific inhibitor of exportin-1 (XPO1), is approved for clinical use. This review will focus on the role of importins and exportins in hematological malignancies. We will discuss current preclinical and clinical data on importins and exportins, and demonstrate how our growing understanding of their functions has identified new therapeutic targets.
引用
收藏
页码:2875 / 2886
页数:12
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