bioRxiv · 10.1101/2020.05.11.089060
Leukemia cell of origin influences apoptotic priming and sensitivity to LSD1 inhibition
Abstract
Previous studies have established that the cell of origin of oncogenic transformation is a determinant of therapeutic sensitivity. However, the mechanisms governing cell-of-origin-driven differences in therapeutic response have not been delineated. Leukemias initiating in hematopoietic stem cells (HSC) are less sensitive to cytotoxic chemotherapy and express high levels of the transcription factor Evi1 compared to leukemias derived from myeloid progenitors. Here, we compared drug sensitivity and expression profiles of murine and human leukemias initiated in either HSCs or myeloid progenitors to reveal a novel function for Evi1 in modulating p53 protein stability and activity. HSC-derived leukemias exhibit decreased apoptotic priming, attenuated p53 transcriptional output, and resistance to lysine-specific demethylase 1 inhibitors in addition to classical genotoxic stresses. p53 loss-of-function in Evi1low progenitor-derived leukemias induces resistance to LSD1 inhibition. By contrast, Evi1high leukemias are sensitized to LSD1 inhibition by the BH3 mimetic venetoclax, resulting in enhanced apoptosis and greater reductions in disease burden. Our findings demonstrate a cell-of-origin determined novel role for EVI1 in p53 wild-type cancers in reducing p53 function and provide a strategy to circumvent drug resistance in high-risk, chemoresistant EVI1high AML.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Cai, S. F., Chu, S. H., Goldberg, A. D., Parvin, S., Koche, R. P., Glass, J. L., Stein, E. M., Tallman, M. S., Sen, F., Famulare, C., Cusan, M., Huang, C.-H., Chen, C.-W., Zou, L., Cordner, K. B., DelGaudio, N. L., Durani, V., Kini, M., Rex, M., Tian, H. S., Zuber, J. L., Baslan, T., Lowe, S. W., Rienhoff, H. Y., Letai, A., Levine, R. L., Armstrong, S. A.. 2020-05-13. Leukemia cell of origin influences apoptotic priming and sensitivity to LSD1 inhibition. https://doi.org/10.1101/2020.05.11.089060
Cite the original work for its findings. Save a collection to share your selection of sources.