The Role of Phase-Separated Condensates in Fusion Oncoprotein–Driven Cancers

IF 4.7 2区 医学 Q1 ONCOLOGY
Hazheen K. Shirnekhi, Bappaditya Chandra, R. Kriwacki
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引用次数: 8

Abstract

Fusion oncoproteins (FOs) resulting from in-frame chromosomal translocations are associated with many aggressive cancers with poor patient outcomes. Several FOs are now understood to perform their oncogenic functions within biomolecular condensates formed through liquid-liquid phase separation (LLPS). Two classes of phase-separating FOs have emerged, those that form nuclear condensates and alter chromatin biology, including gene expression, and those that form cytoplasmic condensates and promote aberrant signaling, including RAS/MAPK signaling. The amino acid sequences of the FOs within these classes display LLPS-prone intrinsically disordered regions and folded domains that synergistically interact with themselves and other biomolecules to promote condensate formation. This review summarizes the roles of LLPS in the oncogenic functions of these two FO classes, provides examples of FOs that inhibit physiological LLPS in normal cells, and discusses the sequence features commonly associated with LLPS and their enrichment in many FOs. Expected final online publication date for the Annual Review of Cancer Biology, Volume 7 is April 2023. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
相分离凝聚物在融合癌蛋白驱动的癌症中的作用
框架内染色体易位引起的融合癌蛋白(FOs)与许多具有不良预后的侵袭性癌症有关。几种FOs现在被理解为在通过液-液相分离(LLPS)形成的生物分子凝聚物中发挥其致癌功能。目前已经出现了两类相分离的FOs,一类形成核凝聚体并改变染色质生物学,包括基因表达,另一类形成细胞质凝聚体并促进异常信号传导,包括RAS/MAPK信号传导。这些类别中的FOs的氨基酸序列显示llps倾向的内在无序区域和折叠区域,这些区域与它们自身和其他生物分子协同作用以促进凝聚物的形成。本文综述了LLPS在这两类FO的致癌功能中的作用,提供了在正常细胞中抑制生理性LLPS的FO的例子,并讨论了与LLPS相关的序列特征及其在许多FO中的富集。预计《癌症生物学年度评论》第七卷的最终在线出版日期是2023年4月。修订后的估计数请参阅http://www.annualreviews.org/page/journal/pubdates。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.50
自引率
1.30%
发文量
13
期刊介绍: The Annual Review of Cancer Biology offers comprehensive reviews on various topics within cancer research, covering pivotal and emerging areas in the field. As our understanding of cancer's fundamental mechanisms deepens and more findings transition into targeted clinical treatments, the journal is structured around three main themes: Cancer Cell Biology, Tumorigenesis and Cancer Progression, and Translational Cancer Science. The current volume of this journal has transitioned from gated to open access through Annual Reviews' Subscribe to Open program, ensuring all articles are published under a CC BY license.
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