A machine learning model identifies M3-like subtype in AML based on PML/RARα targets

The typical genomic feature of acute myeloid leukemia (AML) M3 subtype is the fusion event of PML/RARα, and ATRA/ATO-based combination therapy is current standard treatment regimen for M3 subtype. Here, a machine-learning model based on expressions of PML/RARα targets was developed to identify M3 pa...

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Veröffentlicht in:iScience 2024-02, Vol.27 (2), p.108947, Article 108947
Hauptverfasser: Shao, Tingting, Li, Jianing, Su, Minghai, Yang, Changbo, Ma, Yingying, Lv, Chongwen, Wang, Wei, Xie, Yunjin, Xu, Gang, Shi, Ce, Zhou, Xinying, Fan, Huitao, Li, Yongsheng, Xu, Juan
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Sprache:eng
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Zusammenfassung:The typical genomic feature of acute myeloid leukemia (AML) M3 subtype is the fusion event of PML/RARα, and ATRA/ATO-based combination therapy is current standard treatment regimen for M3 subtype. Here, a machine-learning model based on expressions of PML/RARα targets was developed to identify M3 patients by analyzing 1228 AML patients. Our model exhibited high accuracy. To enable more non-M3 AML patients to potentially benefit from ATRA/ATO therapy, M3-like patients were further identified. We found that M3-like patients had strong GMP features, including the expression patterns of M3 subtype marker genes, the proportion of myeloid progenitor cells, and deconvolution of AML constituent cell populations. M3-like patients exhibited distinct genomic features, low immune activity and better clinical survival. The initiative identification of patients similar to M3 subtype may help to identify more patients that would benefit from ATO/ATRA treatment and deepen our understanding of the molecular mechanism of AML pathogenesis. [Display omitted] •A method based on PML/RARα targets was developed to identify M3 patients•Computational model helps identifying M3 patients with AUCs ranged from 0.965 to 1.00•M3-like patients were with GMP features and would benefit from ATO/ATRA treatment Medical science; Genomics; Machine learning
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2024.108947