KAT6A and KAT7 Histone Acetyltransferase Complexes Are Molecular Dependencies and Therapeutic Targets in <i>NUP98</i> -Rearranged Acute Myeloid Leukemia

KAT6A and KAT7 associate with NUP98 FOs to drive leukemogenesis. Inhibition of their HAT activity is an effective therapeutic strategy in NUP98-r leukemias, including those resistant to menin inhibition. Moreover, combined KAT6A/7 and menin inhibition is synergistic, supporting clinical translation to improve outcomes for NUP98 FO-driven leukemias.

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Publication Details

Journal
Cancer Discovery
Published
2025-06-19
DOI
https://doi.org/10.1158/2159-8290.cd-24-1772
Citations
9
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
7.25

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article

KAT6A and KAT7 Histone Acetyltransferase Complexes Are Molecular Dependencies and Therapeutic Targets in NUP98 -Rearranged Acute Myeloid Leukemia

Francisca N. de Luna Vitorino, Cynthia Martucci, Scott A. Armstrong, Bright Arthur et al.
9 citations
Cancer Discovery
Protein Degradation and Inhibitors
7.25
article

KAT6A and KAT7 Histone Acetyltransferase Complexes Are Molecular Dependencies and Therapeutic Targets in NUP98 -Rearranged Acute Myeloid Leukemia

Francisca N. de Luna Vitorino, Cynthia Martucci, Scott A. Armstrong, Bright Arthur, Daniela V. Wenge, Richard W. Kriwacki, Qingsong Gao, Varsha Subramanyam, Ali Khalighifar, Pradyuamna Baviskar, Ryan Hiltenbrand, Jeffery M. Klco, Vibhor Mishra, Benjamin A. Garcia, Charlie Hatton, Pablo Portola, Evangelia K. Papachristou, Chun Shik Park, David W. Baggett, Charles Grenfell Mullighan, Lingyun Long, Alex Kentsis, Bappaditya Chandra, Ilaria Iacobucci, Chandra Sekhar Reddy Chilamakuri, Stanley Pounds, Hongling Huang, Nicole L. Michmerhuizen, Sandi Radko-Juettner, Hao Shi, Danika Di Giacomo, Laura J. Janke, Hongbo Chi, Emily Heikamp, Huiyun Wu, Yu Sun, Peipei Zhou, Clive S. D’Santos, Joanna M. Gongora, Masayuki Umeda, Aurelie Claquin, Josi Lott
article en
9 citations

Abstract

KAT6A and KAT7 associate with NUP98 FOs to drive leukemogenesis. Inhibition of their HAT activity is an effective therapeutic strategy in NUP98-r leukemias, including those resistant to menin inhibition. Moreover, combined KAT6A/7 and menin inhibition is synergistic, supporting clinical translation to improve outcomes for NUP98 FO-driven leukemias.

Cancer DiscoveryVol. 15(10)
St. Jude Children's Research Hospital (US), Memorial Sloan Kettering Cancer Center (US), Xiamen University (CN), Washington University in St. Louis (US), Cornell University (US), University of Cambridge (GB), University of Perugia (IT), Cancer Research UK (GB), Kettering University (US), Cancer Research UK Cambridge Center (GB), Dana-Farber Cancer Institute (US), Alzheimer’s Research UK (GB), Dana-Farber Brigham Cancer Center (US)
Children's Cancer Research Fund, Charles H. Hood Foundation, Amgen, Pfizer, Leukemia and Lymphoma Society, St. Jude Children's Research Hospital, American Lebanese Syrian Associated Charities, Break Through Cancer, Syndax Pharmaceuticals, European Commission, National Institutes of Health, National Cancer Institute, Hyundai Hope On Wheels
Good health and well-being
Openalex Percentile: Top 3%
Protein Degradation and Inhibitors
7.25
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