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Dissolution of oncofusion transcription factor condensates for cancer therapy.

Yuan WangChunyu YuGaofeng PeiWen JiaTingting LiPilong Li
Published in: Nature chemical biology (2023)
Cancer-associated chromosomal rearrangements can result in the expression of numerous pathogenic fusion proteins. The mechanisms by which fusion proteins contribute to oncogenesis are largely unknown, and effective therapies for fusion-associated cancers are lacking. Here we comprehensively scrutinized fusion proteins found in various cancers. We found that many fusion proteins are composed of phase separation-prone domains (PSs) and DNA-binding domains (DBDs), and these fusions have strong correlations with aberrant gene expression patterns. Furthermore, we established a high-throughput screening method, named DropScan, to screen drugs capable of modulating aberrant condensates. One of the drugs identified via DropScan, LY2835219, effectively dissolved condensates in reporter cell lines expressing Ewing sarcoma fusions and partially rescued the abnormal expression of target genes. Our results indicate that aberrant phase separation is likely a common mechanism for these PS-DBD fusion-related cancers and suggest that modulating aberrant phase separation is a potential route to treat these diseases.
Keyphrases
  • dna binding
  • transcription factor
  • gene expression
  • poor prognosis
  • cancer therapy
  • signaling pathway
  • drug delivery
  • binding protein
  • young adults
  • copy number
  • genome wide
  • organic matter
  • long non coding rna
  • single cell