Multilayer intraclonal heterogeneity in chronic myelomonocytic leukemia

• Published in: Haematologica (Roma) Vol. 105; no. 1; pp. 112 - 123
• Main Authors: Beke, Allan, Laplane, Lucie, Riviere, Julie, Yang, Qin, Torres-Martin, Miguel, Dayris, Thibault, Rameau, Philippe, Saada, Veronique, Bilhou-Nabera, Chrystèle, Hurtado, Ana, Lordier, Larissa, Vainchenker, William, Figueroa, Maria E, Droin, Nathalie, Solary, Eric
• Format: Journal Article
• Language: English
• Published: Italy Ferrata Storti Foundation 01.01.2020
• Subjects: Humans; Leukemia, Myelomonocytic, Chronic - genetics; Leukemia, Myelomonocytic, Juvenile - genetics; Life Sciences; Mutation; Myeloproliferative Disorders; Whole Exome Sequencing
• ISSN: 0390-6078; 1592-8721
• DOI: 10.3324/haematol.2018.208488

The functional diversity of cells that compose myeloid malignancies, i.e., the respective roles of genetic and epigenetic heterogeneity in this diversity, remains poorly understood. This question is addressed in chronic myelomonocytic leukemia, a myeloid neoplasm in which clinical diversity contrasts with limited genetic heterogeneity. To generate induced pluripotent stem cell clones, we reprogrammed CD34 cells collected from a patient with a chronic myelomonocytic leukemia in which whole exome sequencing of peripheral blood monocyte DNA had identified 12 gene mutations, including a mutation in and two heterozygous mutations in in the founding clone and a secondary (G12D) mutation. CD34 cells from an age-matched healthy donor were also reprogrammed. We captured a part of the genetic heterogeneity observed in the patient, i.e. we analyzed five clones with two genetic backgrounds, without and with the (G12D) mutation. Hematopoietic differentiation of these clones recapitulated the main features of the patient's disease, including overproduction of granulomonocytes and dysmegakaryopoiesis. These analyses also disclosed significant discrepancies in the behavior of hematopoietic cells derived from induced pluripotent stem cell clones with similar genetic background, correlating with limited epigenetic changes. These analyses suggest that, beyond the coding mutations, several levels of intraclonal heterogeneity may participate in the yet unexplained clinical heterogeneity of the disease.