International Journal of Molecular Sciences (Feb 2024)

Transcriptome Analysis in Mexican Adults with Acute Lymphoblastic Leukemia

  • Gabriela Marisol Cruz-Miranda,
  • Irma Olarte-Carrillo,
  • Diego Alberto Bárcenas-López,
  • Adolfo Martínez-Tovar,
  • Julian Ramírez-Bello,
  • Christian Omar Ramos-Peñafiel,
  • Anel Irais García-Laguna,
  • Rafael Cerón-Maldonado,
  • Didier May-Hau,
  • Silvia Jiménez-Morales

DOI
https://doi.org/10.3390/ijms25031750
Journal volume & issue
Vol. 25, no. 3
p. 1750

Abstract

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Acute lymphoblastic leukemia (ALL) represents around 25% of adult acute leukemias. Despite the increasing improvement in the survival rate of ALL patients during the last decade, the heterogeneous clinical and molecular features of this malignancy still represent a major challenge for treatment and achieving better outcomes. To identify aberrantly expressed genes in bone marrow (BM) samples from adults with ALL, transcriptomic analysis was performed using Affymetrix Human Transcriptome Array 2.0 (HTA 2.0). Differentially expressed genes (DEGs) (±2-fold change, p-value DNTT, MYB, EBF1, SOX4, and ERG were the top five up-regulated genes. Meanwhile, the top five down-regulated genes were PTGS2, PPBP, ADGRE3, LUCAT1, and VCAN. An association between ERG, CDK6, and SOX4 expression levels and the probability of relapse and death was observed. Regulation of the immune system, immune response, cellular response to stimulus, as well as apoptosis signaling, inflammation mediated by chemokines and cytokines, and T cell activation were among the most altered biological processes and pathways, respectively. Transcriptome analysis of ALL in adults reveals a group of genes consistently associated with hematological malignancies and underscores their relevance in the development of ALL in adults.

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