Multi-platform profiling characterizes molecular subgroups and resistance networks in chronic lymphocytic leukemia

Nat Commun. 2021 Sep 13;12(1):5395. doi: 10.1038/s41467-021-25403-y.

Abstract

Knowledge of the genomic landscape of chronic lymphocytic leukemia (CLL) grows increasingly detailed, providing challenges in contextualizing the accumulated information. To define the underlying networks, we here perform a multi-platform molecular characterization. We identify major subgroups characterized by genomic instability (GI) or activation of epithelial-mesenchymal-transition (EMT)-like programs, which subdivide into non-inflammatory and inflammatory subtypes. GI CLL exhibit disruption of genome integrity, DNA-damage response and are associated with mutagenesis mediated through activation-induced cytidine deaminase or defective mismatch repair. TP53 wild-type and mutated/deleted cases constitute a transcriptionally uniform entity in GI CLL and show similarly poor progression-free survival at relapse. EMT-like CLL exhibit high genomic stability, reduced benefit from the addition of rituximab and EMT-like differentiation is inhibited by induction of DNA damage. This work extends the perspective on CLL biology and risk categories in TP53 wild-type CLL. Furthermore, molecular targets identified within each subgroup provide opportunities for new treatment approaches.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / genetics
  • Chromosome Aberrations
  • DNA Damage
  • DNA Repair
  • Epithelial-Mesenchymal Transition / genetics*
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Leukemic*
  • Gene Regulatory Networks*
  • Genomic Instability*
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Mutation
  • Polymorphism, Single Nucleotide
  • Shelterin Complex
  • Telomere-Binding Proteins / genetics
  • Tumor Suppressor Protein p53 / genetics

Substances

  • POT1 protein, human
  • Shelterin Complex
  • Telomere-Binding Proteins
  • Tumor Suppressor Protein p53
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins