The Affiliated Hospital of Medical School of Ningbo University, Ningbo 315020, China.
State Key Laboratory of Biotherapy and Cancer Center, West China Hospital and West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.
Cells. 2021 Oct 9;10(10):2707. doi: 10.3390/cells10102707.
Following efficient tumor therapy, some cancer cells may survive through a dormancy process, contributing to tumor recurrence and worse outcomes. Dormancy is considered a process where most cancer cells in a tumor cell population are quiescent with no, or only slow, proliferation. Recent advances indicate that redox mechanisms control the dormant cancer cell life cycle, including dormancy entrance, long-term dormancy, and metastatic relapse. This regulatory network is orchestrated mainly through redox modification on key regulators or global change of reactive oxygen species (ROS) levels in dormant cancer cells. Encouragingly, several strategies targeting redox signaling, including sleeping, awaking, or killing dormant cancer cells are currently under early clinical evaluation. However, the molecular mechanisms underlying redox control of the dormant cancer cell cycle are poorly understood and need further exploration. In this review, we discuss the underlying molecular basis of redox signaling in the cell life cycle of dormant cancer and the potential redox-based targeting strategies for eliminating dormant cancer cells.
在有效的肿瘤治疗后,一些癌细胞可能通过休眠过程存活下来,导致肿瘤复发和预后更差。休眠被认为是肿瘤细胞群体中大多数癌细胞处于静止状态,没有或只有缓慢的增殖。最近的进展表明,氧化还原机制控制休眠癌细胞的生命周期,包括休眠进入、长期休眠和转移复发。这个调控网络主要通过关键调节剂的氧化还原修饰或休眠癌细胞中活性氧(ROS)水平的全局变化来协调。令人鼓舞的是,目前正在进行早期临床评估几种针对氧化还原信号的策略,包括休眠癌细胞的休眠、唤醒或杀伤。然而,氧化还原对休眠癌细胞周期调控的分子机制尚不清楚,需要进一步探索。在这篇综述中,我们讨论了氧化还原信号在休眠癌细胞生命周期中的潜在分子基础,以及基于氧化还原的消除休眠癌细胞的潜在靶向策略。