Nuclear Export Gone Rogue: XPO1’s Chromatin Side Hustle Fuels Leukemia

Exportin-1 (XPO1/CRM1) is a validated target in hematologic malignancies best studied for its role in mediating nuclear export. In this issue of Blood Cancer Discovery, Barajas and colleagues reveal that UBTF tandem duplications found in acute myeloid leukemia complete a nuclear export sequence that enables a novel UBTF-XPO1 interaction, particularly at chromatin loci critical for leukemogenesis, thus raising the question: Could XPO1 inhibitors find new use in the UBTF-TD acute myeloid leukemia subtype? See related article by Barajas et al., p. 51.

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Journal
Blood Cancer Discovery
Published
2025-11-20
DOI
https://doi.org/10.1158/2643-3230.bcd-25-0407
Primary Topic
Nuclear Structure and Function
Type
article
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article

Nuclear Export Gone Rogue: XPO1’s Chromatin Side Hustle Fuels Leukemia

Drew Adams
Blood Cancer Discovery
Nuclear Structure and Function
article

Nuclear Export Gone Rogue: XPO1’s Chromatin Side Hustle Fuels Leukemia

Drew Adams
article en

Abstract

Exportin-1 (XPO1/CRM1) is a validated target in hematologic malignancies best studied for its role in mediating nuclear export. In this issue of Blood Cancer Discovery, Barajas and colleagues reveal that UBTF tandem duplications found in acute myeloid leukemia complete a nuclear export sequence that enables a novel UBTF-XPO1 interaction, particularly at chromatin loci critical for leukemogenesis, thus raising the question: Could XPO1 inhibitors find new use in the UBTF-TD acute myeloid leukemia subtype? See related article by Barajas et al., p. 51.

Blood Cancer DiscoveryVol. 7(1)
Case Western Reserve University (US)
Openalex Percentile: Top 68%
Nuclear Structure and Function
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