MiRNAs from the Dlk1-Dio3 locus and miR-224/452 cluster contribute to glioblastoma tumor heterogeneity

Sci Rep. 2024 Apr 13;14(1):8570. doi: 10.1038/s41598-024-58870-6.

Abstract

Glioblastoma is one of the most common and aggressive brain tumors and has seen few improvements in patient outcomes. Inter-tumor heterogeneity between tumors of different patients as well as intra-tumor heterogeneity of cells within the same tumor challenge the development of effective drugs. MiRNAs play an essential role throughout the developing brain and regulate many key genes involved in oncogenesis, yet their role in driving many of the processes underlying tumor heterogeneity remains unclear. In this study, we highlight miRNAs from the Dlk1-Dio3 and miR-224/452 clusters which may be expressed cell autonomously and have expression that is associated with cell state genes in glioblastoma, most prominently in neural progenitor-like and mesenchymal-like states respectively. These findings implicate these miRNA clusters as potential regulators of glioblastoma intra-tumoral heterogeneity and may serve as valuable biomarkers for cell state identification.

MeSH terms

  • Brain
  • Brain Neoplasms* / genetics
  • Carcinogenesis
  • Glioblastoma* / genetics
  • Humans
  • MicroRNAs* / genetics

Substances

  • MicroRNAs
  • MIRN224 microRNA, human
  • MIRN452 microRNA, human
  • DLK1 protein, human
  • iodothyronine deiodinase type III