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| Item Type: | Article |
|---|---|
| Title: | Molecular plasticity results in oncofetal reprogramming and therapeutic vulnerabilities in juvenile myelomonocytic leukemia |
| Creators Name: | Hartmann, Mark, Schönung, Maximilian, Rajak, Jovana, Maurer, Valentin, Hai, Ling, Bauer, Katharina, Hakobyan, Mariam, Stäble, Sina, Langstein, Jens, Jardine, Laura, Roelz, Roland, Bohler, Sheila, Khabirova, Eleonora, Maag, Abdul-Habib, Vonficht, Dominik, Lebrecht, Dirk, Bernt, Kathrin M., Tan, Kai, Chen, Changya, Alikarami, Fatemeh, Meyer, Julia, Wang, Jun, Boch, Tobias, Flore, Viktoria, Lutsik, Pavlo, Milsom, Michael D., Raffel, Simon, Buske, Christian, Haas, Simon, Haniffa, Muzlifah, Mallm, Jan-Philipp, Behjati, Sam, Bonder, Marc-Jan, Fröhling, Stefan, Stieglitz, Elliot, Niemeyer, Charlotte M., Hey, Joschka, Flotho, Christian, Plass, Christoph, Erlacher, Miriam, Schlesner, Matthias and Lipka, Daniel B. |
| Abstract: | Persistent fetal gene expression in childhood neoplasms is usually explained by a maturation block originating in the prenatal phase. In contrast, reactivation of fetal genes in adult malignancies is considered a consequence of oncofetal reprogramming (OFR) and is associated with aggressive disease. By reconstructing epigenetic ontogeny in juvenile myelomonocytic leukemia (JMML), we identified a postnatal maturation state of JMML stem cells with high transcriptional plasticity indicative of OFR in high-risk disease. Similarly, post-natal activation of oncogenic signaling by inducible Ptpn11E76K mutation in mice, triggered molecular plasticity and reactivation of fetal gene expression. Integrative multi-omics analysis revealed aberrant CD52 expression as a feature of high-risk JMML stem cells. Anti-CD52 treatment depleted JMML stem cells and blocked disease propagation in xenograft models. Our results challenge the prevailing maturation-block model of pediatric leukemogenesis and establish RAS-associated stem-cell plasticity as a determinant of OFR and potential therapeutic vulnerabilities in high-risk JMML. STATEMENT OF SIGNIFICANCE: Persistent fetal gene expression in pediatric malignancies is considered a consequence of prenatal maturation blockade. Here, we demonstrate that oncogenic PTPN11 mutations enhance cellular plasticity. This leads to partial restoration of fetal molecular programs, creating new therapeutically exploitable vulnerabilities. |
| Source: | Blood Cancer Discovery |
| ISSN: | 2643-3230 |
| Publisher: | American Association for Cancer Research |
| Date: | 5 December 2025 |
| Official Publication: | https://doi.org/10.1158/2643-3230.bcd-25-0246 |
| PubMed: | View item in PubMed |
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