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Updated: Jul 24, 2025

Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic Analysis
Published on: June 27, 2020
Dissolution of oncofusion transcription factor condensates for cancer therapy
Yuan Wang1,2, Chunyu Yu3,4, Gaofeng Pei1,2
1State Key Laboratory of Membrane Biology, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing, China.
Abstract:
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.
Insights
Cancer chromosomal rearrangements create fusion proteins driving oncogenesis. Aberrant phase separation by these proteins is a common mechanism, suggesting therapies targeting this process could treat these cancers.
Area of Science:
- Molecular Oncology
- Biochemistry
- Genetics
Background:
- Cancer-associated chromosomal rearrangements lead to pathogenic fusion proteins.
- Mechanisms of fusion protein oncogenesis and therapies are poorly understood.
Purpose of the Study:
- To investigate the role of fusion proteins in oncogenesis.
- To identify therapeutic strategies for fusion-associated cancers.
Main Methods:
- Comprehensive analysis of fusion proteins across various cancers.
- Development of DropScan, a high-throughput screening method for drugs modulating aberrant condensates.
- Testing drug efficacy in reporter cell lines.
Main Results:
- Many fusion proteins contain phase separation-prone domains (PSs) and DNA-binding domains (DBDs).
- These fusions correlate with aberrant gene expression.
- DropScan identified LY2835219, which dissolved condensates and partially rescued gene expression in Ewing sarcoma models.
Conclusions:
- Aberrant phase separation is a likely common mechanism in PS-DBD fusion-related cancers.
- Modulating aberrant phase separation presents a potential therapeutic strategy for these cancers.
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