The novel TERF2::PDGFRB fusion gene enhances tumorigenesis via PDGFRB/STAT5 signalling pathways and sensitivity to TKI in ph-like ALL

J Cell Mol Med. 2024 Feb;28(3):e18114. doi: 10.1111/jcmm.18114.

Abstract

Patients with Philadelphia chromosome-like acute lymphoblastic leukaemia (Ph-like ALL) often face a grim prognosis, with PDGFRB gene fusions being commonly detected in this subgroup. Our study has unveiled a newfound fusion gene, TERF2::PDGFRB, and we have found that patients carrying this fusion gene exhibit sensitivity to dasatinib. Ba/F3 cells harbouring the TERF2::PDGFRB fusion display IL-3-independent cell proliferation through activation of the p-PDGFRB and p-STAT5 signalling pathways. These cells exhibit reduced apoptosis and demonstrate sensitivity to imatinib in vitro. When transfused into mice, Ba/F3 cells with the TERF2::PDGFRB fusion gene induce tumorigenesis and a shortened lifespan in cell-derived graft models, but this outcome can be improved with imatinib treatment. In summary, we have identified the novel TERF2::PDGFRB fusion gene, which exhibits oncogenic potential both in vitro and in vivo, making it a potential therapeutic target for tyrosine kinase inhibitors (TKIs).

Keywords: CDX; Ph-like acute lymphoblastic leukaemia; STAT5; TERF2::PDGFRB; TKI.

MeSH terms

  • Animals
  • Carcinogenesis
  • Cell Transformation, Neoplastic
  • Humans
  • Imatinib Mesylate
  • Mice
  • Oncogene Proteins, Fusion* / genetics
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / genetics
  • Protein Kinase Inhibitors / pharmacology
  • Receptor, Platelet-Derived Growth Factor beta* / genetics
  • STAT5 Transcription Factor / genetics
  • Signal Transduction
  • Telomeric Repeat Binding Protein 2* / genetics

Substances

  • Imatinib Mesylate
  • PDGFRB protein, human
  • Protein Kinase Inhibitors
  • Receptor, Platelet-Derived Growth Factor beta
  • STAT5 Transcription Factor
  • Telomeric Repeat Binding Protein 2
  • TERF2 protein, human
  • Oncogene Proteins, Fusion