BAALC gene expression tells a serious patient outcome tale in NPM1-wild type/FLT3-ITD negative cytogenetically normal-acute myeloid leukemia in adults

Blood Cells Mol Dis. 2022 Jul:95:102662. doi: 10.1016/j.bcmd.2022.102662. Epub 2022 Apr 8.

Abstract

Acute myeloid leukemia with normal cytogenetics (CN-AML) is the largest group of AML patients which is associated with a variegated patient outcome. Multiple molecular markers have been used to risk-stratify these patients. Estimation of expression of BAALC gene (Brain and Acute Leukemia, Cytoplasmic) mRNA level is one of the predictive markers which has been identified in multiple studies. In this study, we examined the clinical and prognostic value of BAALC gene expression in 149 adult CN-AML patients. We also utilized multi-omics databases to ascertain the association of BAALC gene expression with comprehensive molecular and clinicopathologic features in AML. BAALC overexpression was associated with CD34 positivity on leukemic blasts (p = 0.0026) and the absence of NPM1 gene mutation (p < 0.0001), presence of RUNX1 gene mutation (p < 0.001) and poor patient outcomes, particularly in NPM1-wild type/FLT3-ITD negative adult CN-AML patients. Additionally, BAALC expression was associated with the alteration of methylation of its promoter. Further, pathway analysis revealed that BAALC expression is correlated with MYC targets and Ras signalling. We conclude that high BAALC expression associates with poor patient outcome in NPM1-wild type/FLT3-ITD negative adult CN-AML patients.

Keywords: AML; BAALC; Gene expression; Prognosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Gene Expression
  • Humans
  • Leukemia, Myeloid, Acute* / genetics
  • Mutation
  • Neoplasm Proteins / genetics
  • Nuclear Proteins / genetics
  • Prognosis
  • Transcription Factors / genetics
  • fms-Like Tyrosine Kinase 3 / genetics

Substances

  • BAALC protein, human
  • Neoplasm Proteins
  • Nuclear Proteins
  • Transcription Factors
  • FLT3 protein, human
  • fms-Like Tyrosine Kinase 3