Characterization of the clonal hierarchy and immunophenotype of PTPN11 mutations in acute myeloid leukemia.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Fobare Sydney, Sharpe Chia, Quinn Kate, Bryant Kinsey, Miles Linde A, Bowman Robert L, Cheney Carolyn, Furby Casie, Long Marissa, Fyock Kaytlynn, Wronowski Ben, Lerma James R, Mrózek Krzysztof, Nicolet Deedra, Sesterhenn Thomas M, Johnstone Megan E, Pan Jianmin, Rai Shesh N, Pasare Chandrashekhar, Zimmermann Nives, Yu Wen-Mei, Qu Cheng-Kui, Carroll Andrew, Stone Richard, Wang Eunice S, Kolitz Jonathan, Powell Bayard, Perentesis John P, Eisfeld Ann-Kathrin, Hertlein Erin, Byrd John C
Аннотация
Mutations in protein tyrosine phosphatase non-receptor type 11 (PTPN11) have been considered late acquired mutations in acute myeloid leukemia (AML) development. Using single-cell DNA sequencing, we found that PTPN11 mutations can occur as initiating events in some patients with AML when accompanied by strong oncogenic drivers, commonly NPM1 mutations. The resulting AML has a diverse set of variably differentiated myeloid cells with few myeloid cells that lack leukemic mutations. The role of Ptpn11 as a codriver was confirmed in a murine model that exhibits an AML phenotype with a comparable immune diversity that is serially engraftable and reconstituted from early precursor cells. Furthermore, lineage-negative bone marrow cells from these mice reconstitute the full diversity of mature myeloid cells, and these cells exhibit an altered cytokine response after physiologic stimulation. Our work highlights how PTPN11-mutated AML is derived from a multitude of codominant and late acquired aberrations that have a previously unrecognized differentiated myeloid clonal expansion potentially contributing to pathogenesis of the disease.