对于ecDNA聚合物的相分离,可以建立in-trans接触域,从而促进选择性MYC调节相互作用
Mattia Conte1, Tommaso Matteuzzi1, Andrea Esposito1
1Dipartimento di Fisica, Università di Napoli Federico II, and INFN Napoli, Complesso Universitario di Monte Sant'Angelo, 80126 Naples, Italy.
bioRxiv : the preprint server for biology
|July 28, 2023
概括
BRD4蛋白驱动癌细胞中的异染色体DNA (ecDNA) 聚类,产生调节接触,放大MYC瘤基因表达. 这种ecDNA聚合机制对于理解癌症进展和开发向疗法至关重要.
科学领域:
- 癌症生物学 癌症生物学
- 分子瘤学分子瘤学
- 基因组学就是基因组学.
背景情况:
- 染色体外DNA (ecDNA) 含有瘤基因,并通过基因放大促进癌症的发展.
- 基于ecDNA聚合的机制及其在癌基因过度表达中的作用超出了简单的副本数量的变化还没有完全理解.
结论:
- 这项研究揭示了由BRD4驱动的ecDNA聚类在放大结直肠癌细胞中MYC瘤基因表达方面发挥着关键作用.
- BET 抑制剂 JQ1 破坏 ecDNA 阶段分离并消除 I-TAD,减少 MYC 转录并提供治疗策略.
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