Understanding glioblastoma at the single-cell level: Recent advances and future challenges.
Yahaya A YaboDieter Henrik HeilandPublished in: PLoS biology (2024)
Glioblastoma, the most aggressive and prevalent form of primary brain tumor, is characterized by rapid growth, diffuse infiltration, and resistance to therapies. Intrinsic heterogeneity and cellular plasticity contribute to its rapid progression under therapy; therefore, there is a need to fully understand these tumors at a single-cell level. Over the past decade, single-cell transcriptomics has enabled the molecular characterization of individual cells within glioblastomas, providing previously unattainable insights into the genetic and molecular features that drive tumorigenesis, disease progression, and therapy resistance. However, despite advances in single-cell technologies, challenges such as high costs, complex data analysis and interpretation, and difficulties in translating findings into clinical practice persist. As single-cell technologies are developed further, more insights into the cellular and molecular heterogeneity of glioblastomas are expected, which will help guide the development of personalized and effective therapies, thereby improving prognosis and quality of life for patients.
Keyphrases
- single cell
- rna seq
- high throughput
- data analysis
- clinical practice
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- stem cells
- genome wide
- cell proliferation
- low grade
- dna methylation
- single molecule
- copy number
- cell death
- cell cycle arrest
- loop mediated isothermal amplification
- cell therapy
- high grade
- smoking cessation