Abstract

The treatment landscape of AML is evolving with promising therapies entering clinical translation, yet patient responses remain heterogeneous and biomarkers for tailoring treatment are lacking. To understand how disease heterogeneity links with therapy response, we determined the leukemia cell hierarchy make-up from bulk transcriptomes of over 1000 patients through deconvolution using single-cell reference profiles of leukemia stem, progenitor, and mature cell types. Leukemia hierarchy composition was associated with functional, genomic, and clinical properties and converged into four overall classes, spanning Primitive, Mature, GMP, and Intermediate. Critically, variation in hierarchy composition along the Primitive vs GMP or Primitive vs Mature axes were associated with response to chemotherapy or drug sensitivity profiles of targeted therapies, respectively. A 7-gene biomarker derived from the Primitive vs Mature axis was predictive of patient response to 105 investigational drugs. Thus, hierarchy composition constitutes a novel framework for understanding disease biology and advancing precision medicine in AML.

Competing Interest Statement

The authors have declared no competing interest.

Details

Title
A cellular hierarchy framework for understanding heterogeneity and predicting drug response in AML
Author
Zeng, Andy Gx; Bansal, Suraj; Jin, Liqing; Mitchell, Amanda; Chen, Weihsu Claire; Abbas, Hussein A; Chan-Seng-Yue, Michelle; Voisin, Veronique; Peter Van Galen; Tierens, Anne; Cheok, Meyling; Preudhomme, Claude; Dombret, Hervé; Daver, Naval; Futreal, P Andrew; Minden, Mark D; Kennedy, James A; Wang, Jean Cy; Dick, John E
University/institution
Cold Spring Harbor Laboratory Press
Section
New Results
Publication year
2022
Publication date
Jan 27, 2022
Publisher
Cold Spring Harbor Laboratory Press
Source type
Working Paper
Language of publication
English
ProQuest document ID
2623195775
Copyright
© 2022. This article is published under http://creativecommons.org/licenses/by-nd/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.