4.7 Article

Super-enhancer associated core regulatory circuits mediate susceptibility to retinoic acid in neuroblastoma cells

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.943924

关键词

neuroblastoma; super-enhancers; retinoic acid; differentiation; treatment-resistance

资金

  1. Terry Fox Foundation
  2. Al Jalila Foundation
  3. MBRU College of Medicine Internal grant award [MBRU-CM-RG2019-14]
  4. MBRU ALMAHMEED Collaborative Research Award [ALM1909]
  5. Neuroblastoma UK
  6. Cancer Research UK Programme Grant [A25636]
  7. Wellcome Trust Investigator Award [212253/Z/18/Z]
  8. Wellcome Trust [203151/Z/16/Z]
  9. UKRI Medical Research Council [MC_PC_17230]
  10. Wellcome Trust [212253/Z/18/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

This study identifies the differential super-enhancer landscape between different cell types in neuroblastoma, which may contribute to the diverse response to retinoic acid. The study also identifies key super-enhancers responsible for maintaining differentiation.
Neuroblastoma is a pediatric tumour that accounts for more than 15% of cancer-related deaths in children. High-risk tumours are often difficult to treat, and patients' survival chances are less than 50%. Retinoic acid treatment is part of the maintenance therapy given to neuroblastoma patients; however, not all tumours differentiate in response to retinoic acid. Within neuroblastoma tumors, two phenotypically distinct cell types have been identified based on their super-enhancer landscape and transcriptional core regulatory circuitries: adrenergic (ADRN) and mesenchymal (MES). We hypothesized that the distinct super-enhancers in these different tumour cells mediate differential response to retinoic acid. To this end, three different neuroblastoma cell lines, ADRN (MYCN amplified and non amplified) and MES cells, were treated with retinoic acid, and changes in the super-enhancer landscape upon treatment and after subsequent removal of retinoic acid was studied. Using ChIP-seq for the active histone mark H3K27ac, paired with RNA-seq, we compared the super-enhancer landscape in cells that undergo neuronal differentiation in response to retinoic acid versus those that fail to differentiate and identified unique super-enhancers associated with neuronal differentiation. Among the ADRN cells that respond to treatment, MYCN-amplified cells remain differentiated upon removal of retinoic acid, whereas MYCN non-amplified cells revert to an undifferentiated state, allowing for the identification of super-enhancers responsible for maintaining differentiation. This study identifies key super-enhancers that are crucial for retinoic acid-mediated differentiation.

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