Bevinakoppamath Supriya, Ramachandra Shobha Chikkavaddaragudi, Yadav Anshu Kumar, Basavaraj Vijaya, Vishwanath Prashant, Prashant Akila
Center of Excellence in Molecular Biology and Regenerative Medicine, Department of Biochemistry, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India.
Department of Pathology, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India.
Front Pharmacol. 2022 Jan 19;12:719631. doi: 10.3389/fphar.2021.719631. eCollection 2021.
The levels of different molecules in the cell are rhythmically cycled by the molecular clock present at the cellular level. The circadian rhythm is closely linked to the metabolic processes in the cells by an underlying mechanism whose intricacies need to be thoroughly investigated. Nevertheless, Nrf2 has been identified as an essential bridge between the circadian clock and cellular metabolism and is activated by the by-product of cellular metabolism like hydrogen peroxide. Once activated it binds to the specific DNA segments and increases the transcription of several genes that play a crucial role in the normal functioning of the cell. The central clock located in the suprachiasmatic nucleus of the anterior hypothalamus synchronizes the timekeeping in the peripheral tissues by integrating the light-dark input from the environment. Several studies have demonstrated the role of circadian rhythm as an effective tumor suppressor. Tumor development is triggered by the stimulation or disruption of signaling pathways at the cellular level as a result of the interaction between cells and environmental stimuli. Oxidative stress is one such external stimulus that disturbs the prooxidant/antioxidant equilibrium due to the loss of control over signaling pathways which destroy the bio-molecules. Altered Nrf2 expression and impaired redox balance are associated with various cancers suggesting that Nrf2 targeting may be used as a novel therapeutic approach for treating cancers. On the other hand, Nrf2 has also been shown to enhance the resistance of cancer cells to chemotherapeutic agents. We believe that maximum efficacy with minimum side effects for any particular therapy can be achieved if the treatment strategy regulates the circadian rhythm. In this review, we discuss the various molecular mechanisms interlinking the circadian rhythm with the Nrf2 pathway and contributing to breast cancer pathogenesis, we also talk about how these two pathways work in close association with the cell cycle which is another oscillatory system, and whether this interplay can be exploited to overcome drug resistance during chemotherapy.
细胞中不同分子的水平由细胞水平存在的分子时钟进行节律性循环。昼夜节律通过一种潜在机制与细胞中的代谢过程紧密相连,其复杂性需要深入研究。然而,Nrf2已被确定为昼夜节律与细胞代谢之间的重要桥梁,并被细胞代谢的副产物如过氧化氢激活。一旦被激活,它就会与特定的DNA片段结合,并增加几个对细胞正常功能起关键作用的基因的转录。位于下丘脑前部视交叉上核的中央时钟通过整合来自环境的明暗输入来同步外周组织的计时。多项研究已证明昼夜节律作为一种有效的肿瘤抑制因子的作用。肿瘤的发展是由于细胞与环境刺激之间的相互作用,在细胞水平上信号通路受到刺激或破坏而引发的。氧化应激就是这样一种外部刺激,它由于对破坏生物分子的信号通路失去控制而扰乱了促氧化剂/抗氧化剂的平衡。Nrf2表达改变和氧化还原平衡受损与多种癌症相关,这表明靶向Nrf2可能用作治疗癌症的一种新的治疗方法。另一方面,Nrf2也已被证明可增强癌细胞对化疗药物的抗性。我们认为,如果治疗策略能够调节昼夜节律,那么任何特定治疗都可以实现疗效最大化且副作用最小化。在这篇综述中,我们讨论了将昼夜节律与Nrf2途径相互联系并促成乳腺癌发病机制的各种分子机制,我们还讨论了这两条途径如何与另一个振荡系统——细胞周期密切相关,以及这种相互作用是否可被利用来克服化疗期间的耐药性。