Precision Medicine Highlights Dysregulation of the CDK4/6 Cell Cycle Regulatory Pathway in Pediatric, Adolescents and Young Adult Sarcomas.
Farinaz BarghiHarlan E ShannonM Reza SaadatzadehBarbara J BaileyNiknam RiyahiKhadijeh Bijangi-VishehsaraeiMarissa JustMichael J FergusonPankita H PandyaKaren E PollokPublished in: Cancers (2022)
Despite improved therapeutic and clinical outcomes for patients with localized diseases, outcomes for pediatric and AYA sarcoma patients with high-grade or aggressive disease are still relatively poor. With advancements in next generation sequencing (NGS), precision medicine now provides a strategy to improve outcomes in patients with aggressive disease by identifying biomarkers of therapeutic sensitivity or resistance. The integration of NGS into clinical decision making not only increases the accuracy of diagnosis and prognosis, but also has the potential to identify effective and less toxic therapies for pediatric and AYA sarcomas. Genome and transcriptome profiling have detected dysregulation of the CDK4/6 cell cycle regulatory pathway in subpopulations of pediatric and AYA OS, RMS, and EWS. In these patients, the inhibition of CDK4/6 represents a promising precision medicine-guided therapy. There is a critical need, however, to identify novel and promising combination therapies to fight the development of resistance to CDK4/6 inhibition. In this review, we offer rationale and perspective on the promise and challenges of this therapeutic approach.
Keyphrases
- cell cycle
- high grade
- cell proliferation
- young adults
- end stage renal disease
- decision making
- chronic kidney disease
- single cell
- low grade
- gene expression
- transcription factor
- genome wide
- ejection fraction
- clinical trial
- risk assessment
- bone marrow
- rna seq
- peritoneal dialysis
- prognostic factors
- type diabetes
- dna methylation
- machine learning
- mesenchymal stem cells
- patient reported outcomes
- copy number
- adipose tissue
- glycemic control
- climate change
- insulin resistance
- weight loss
- circulating tumor cells
- cell free