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Updated: May 1, 2026

Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
Mutations in epigenetic regulators including SETD2 are gained during relapse in paediatric acute lymphoblastic
Brenton G Mar1, Lars B Bullinger2, Kathleen M McLean3
11] Department of Pediatric Oncology, Dana Farber Cancer Institute, Boston, Massachusetts 02215, USA [2] Department of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts 02115, USA.
Abstract:
Relapsed paediatric acute lymphoblastic leukaemia (ALL) has high rates of treatment failure. Epigenetic regulators have been proposed as modulators of chemoresistance, here, we sequence genes encoding epigenetic regulators in matched diagnosis-remission-relapse ALL samples. We find significant enrichment of mutations in epigenetic regulators at relapse with recurrent somatic mutations in SETD2, CREBBP, MSH6, KDM6A and MLL2, mutations in signalling factors are not enriched. Somatic alterations in SETD2, including frameshift and nonsense mutations, are present at 12% in a large de novo ALL patient cohort. We conclude that the enrichment of mutations in epigenetic regulators at relapse is consistent with a role in mediating therapy resistance.
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