Single-Cell Gene Expression Analyses Reveal Distinct Self-Renewing and Proliferating Subsets in the Leukemia Stem Cell Compartment in Acute Myeloid Leukemia
Karen Sachs,Aaron L. Sarver,Klara E. Noble-Orcutt,Rebecca S. LaRue,Marie Lue Antony,Daniel Chang,Yoonkyu Lee,Connor M. Navis,Alexandria L. Hillesheim,Ian R. Nykaza,Ngoc A. Ha,Conner J. Hansen,Fatma Keklik Karadağ,Rachel J. Bergerson,Michael R. Verneris,Matthew M. Meredith,Matthew Schomaker,Michael A. Linden,Chad L. Myers,David A. Largaespada
出处
期刊:Cancer Research [American Association for Cancer Research] 日期:2019-11-29卷期号:80 (3): 458-470被引量:53
Standard chemotherapy for acute myeloid leukemia (AML) targets proliferative cells and efficiently induces complete remission; however, many patients relapse and die of their disease. Relapse is caused by leukemia stem cells (LSC), the cells with self-renewal capacity. Self-renewal and proliferation are separate functions in normal hematopoietic stem cells (HSC) in steady-state conditions. If these functions are also separate functions in LSCs, then antiproliferative therapies may fail to target self-renewal, allowing for relapse. We investigated whether proliferation and self-renewal are separate functions in LSCs as they often are in HSCs. Distinct transcriptional profiles within LSCs of