Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Trends Cell Biol. 2022 Jan;32(1):30-44. doi: 10.1016/j.tcb.2021.07.001. Epub 2021 Jul 22.
Aberrancy in cell cycle progression is one of the fundamental mechanisms underlying tumorigenesis, making regulators of the cell cycle machinery rational anticancer therapeutic targets. A growing body of evidence indicates that the cell cycle regulatory pathway integrates into other hallmarks of cancer, including metabolism remodeling and immune escape. Thus, therapies against cell cycle machinery components can not only repress the division of cancer cells, but also reverse cancer metabolism and restore cancer immune surveillance. Besides the ongoing effects on the development of small molecule inhibitors (SMIs) of the cell cycle machinery, proteolysis targeting chimeras (PROTACs) have recently been used to target these oncogenic proteins related to cell cycle progression. Here, we discuss the rationale of cell cycle targeting therapies, particularly PROTACs, to more efficiently retard tumorigenesis.
细胞周期进展异常是肿瘤发生的基本机制之一,因此细胞周期调控机制成为了合理的抗癌治疗靶点。越来越多的证据表明,细胞周期调控途径与癌症的其他特征(包括代谢重塑和免疫逃逸)相整合。因此,针对细胞周期机制成分的治疗不仅可以抑制癌细胞的分裂,还可以逆转癌症代谢并恢复癌症免疫监视。除了对细胞周期机制小分子抑制剂(SMIs)的持续开发外,最近还使用蛋白水解靶向嵌合体(PROTACs)来靶向与细胞周期进展相关的这些致癌蛋白。在这里,我们讨论了针对细胞周期的治疗方法,特别是 PROTACs,以更有效地抑制肿瘤发生的原理。