Transcriptional immune suppression and up-regulation of double-stranded DNA damage and repair repertoires in ecDNA-containing tumors.
Miin S LinSe-Young JoJens LuebeckHoward Y ChangSihan WuPaul S MischelVineet BafnaPublished in: eLife (2024)
Extrachromosomal DNA is a common cause of oncogene amplification in cancer. The non-chromosomal inheritance of ecDNA enables tumors to rapidly evolve, contributing to treatment resistance and poor outcome for patients. The transcriptional context in which ecDNAs arise and progress, including chromosomally-driven transcription, is incompletely understood. We examined gene expression patterns of 870 tumors of varied histological types, to identify transcriptional correlates of ecDNA. Here, we show that ecDNA-containing tumors impact four major biological processes. Specifically, ecDNA-containing tumors up-regulate DNA damage and repair, cell cycle control, and mitotic processes, but down-regulate global immune regulation pathways. Taken together, these results suggest profound alterations in gene regulation in ecDNA-containing tumors, shedding light on molecular processes that give rise to their development and progression.
Keyphrases
- gene expression
- dna damage
- cell cycle
- transcription factor
- oxidative stress
- end stage renal disease
- cell proliferation
- dna methylation
- newly diagnosed
- chronic kidney disease
- single molecule
- ejection fraction
- squamous cell carcinoma
- young adults
- dna repair
- nucleic acid
- intellectual disability
- papillary thyroid
- autism spectrum disorder
- combination therapy
- squamous cell
- label free