DNMT3AR882H Is Not Required for Disease Maintenance in Primary Human AML, but Is Associated With Increased Leukemia Stem Cell Frequency

作者：Thomas Köhnke, Daiki Karigane, Eleanor Hilgart, Amy C. Fan, Kensuke Kayamori, Masashi Miyauchi, Cailin Collins, Fabian P. Suchy, Athreya Rangavajhula, Yang Feng, Yusuke Nakauchi, Eduardo Martínez‐Montes, Jonas L. Fowler, Kyle M. Loh, Hiromitsu Nakauchi, Michael A. Koldobskiy, Andrew P. Feinberg, Ravindra Majeti · 发表于：bioRxiv (Cold Spring Harbor Laboratory) · 年份：2024 · DOI：10.1101/2024.10.26.620318 · 被引用次数：3 · 研究领域：Acute Myeloid Leukemia Research、Histone Deacetylase Inhibitors Research、CRISPR and Genetic Engineering

Genetic mutations are being thoroughly mapped in human cancers, yet a fundamental question in cancer biology is whether such mutations are functionally required for cancer initiation, maintenance of established cancer, or both. Here, we study this question in the context of human acute myeloid leukemia (AML), where DNMT3AR882 missense mutations often arise early, in pre-leukemic clonal hematopoiesis, and corrupt the DNA methylation landscape to initiate leukemia. We developed CRISPR-based methods to directly correct DNMT3AR882 mutations in leukemic cells obtained from patients. Surprisingly, DNMT3AR882 mutations were largely dispensable for disease maintenance. Replacing DNMT3AR882 mutants with wild-type DNMT3A did not impair the ability of AML cells to engraft in vivo, and minimally altered DNA methylation. Taken together, DNMT3AR882 mutations are initially necessary for AML initiation, but are largely dispensable for disease maintenance. The notion that initiating oncogenes differ from those that maintain cancer has important implications for cancer evolution and therapy.