The oncogenic circular RNA circ_63706 is a potential therapeutic target in sonic hedgehog-subtype childhood medulloblastomas.
Keisuke KatsushimaRudramani PokhrelIqbal MahmudMenglang YuanRabi MuradPrabin BaralRui ZhouPrem ChapagainTimothy GarrettStacie StapletonGeorge JalloChetan BettegowdaEric RaabeRobert J Wechsler-ReyaCharles G EberhartRanjan J PereraPublished in: Acta neuropathologica communications (2023)
Medulloblastoma (MB) develops through various genetic, epigenetic, and non-coding (nc) RNA-related mechanisms, but the roles played by ncRNAs, particularly circular RNAs (circRNAs), remain poorly defined. CircRNAs are increasingly recognized as stable non-coding RNA therapeutic targets in many cancers, but little is known about their function in MBs. To determine medulloblastoma subgroup-specific circRNAs, publicly available RNA sequencing (RNA-seq) data from 175 MB patients were interrogated to identify circRNAs that differentiate between MB subgroups. circ_63706 was identified as sonic hedgehog (SHH) group-specific, with its expression confirmed by RNA-FISH analysis in clinical tissue samples. The oncogenic function of circ_63706 was characterized in vitro and in vivo. Further, circ_63706-depleted cells were subjected to RNA-seq and lipid profiling to identify its molecular function. Finally, we mapped the circ_63706 secondary structure using an advanced random forest classification model and modeled a 3D structure to identify its interacting miRNA partner molecules. Circ_63706 regulates independently of the host coding gene pericentrin (PCNT), and its expression is specific to the SHH subgroup. circ_63706-deleted cells implanted into mice produced smaller tumors, and mice lived longer than parental cell implants. At the molecular level, circ_63706-deleted cells elevated total ceramide and oxidized lipids and reduced total triglyceride. Our study implicates a novel oncogenic circular RNA in the SHH medulloblastoma subgroup and establishes its molecular function and potential as a future therapeutic target.
Keyphrases
- single cell
- rna seq
- induced apoptosis
- cell cycle arrest
- end stage renal disease
- poor prognosis
- endoplasmic reticulum stress
- transcription factor
- deep learning
- gene expression
- single molecule
- newly diagnosed
- chronic kidney disease
- genome wide
- clinical trial
- stem cells
- climate change
- oxidative stress
- randomized controlled trial
- mesenchymal stem cells
- cell therapy
- machine learning
- metabolic syndrome
- high fat diet induced
- insulin resistance
- fatty acid
- risk assessment
- peritoneal dialysis
- human health
- long non coding rna
- young adults
- patient reported
- protein kinase