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靶向铁死亡关键通路并增强铂类药物治疗结直肠癌的抗肿瘤作用。

Targeting critical pathways in ferroptosis and enhancing antitumor therapy of Platinum drugs for colorectal cancer.

机构信息

Department of Pharmaceutics, Shanghai Eighth People's Hospital, 12676Jiangsu University, Shanghai, China.

Department of Medicine, 12676Jiangsu University, Zhenjiang City, Jiangsu Province, China.

出版信息

Sci Prog. 2023 Jan-Mar;106(1):368504221147173. doi: 10.1177/00368504221147173.

Abstract

Colorectal cancer (CRC) can be resistant to platinum drugs, possibly through ferroptosis suppression, albeit the need for further work to completely understand this mechanism. This work aimed to sum up current findings pertaining to oxaliplatin resistance (OR) or resistance to ascertain the potential of ferroptosis to regulate oxaliplatin effects. In this review, tumor development relating to iron homeostasis, which includes levels of iron that ascertain cells' sensitivity to ferroptosis, oxidative stress, or lipid peroxidation in colorectal tumor cells that are connected with ferroptosis initiation, especially the role of c-Myc/NRF2 signaling in regulating iron homeostasis, coupled with NRF2/GPX4-mediated ferroptosis are discussed. Importantly, ferroptosis plays a key role in OR and ferroptotic induction may substantially reverse OR in CRC cells, which in turn could inhibit the imbalance of intracellular redox induced by oxaliplatin and ferroptosis, as well as cause chemotherapeutic resistance in CRC. Furthermore, fundamental research of small molecules, ferroptosis inducers, GPX4 inhibitors, or natural products for OR coupled with their clinical applications in CRC have also been summarized. Also, potential molecular targets and mechanisms of small molecules or drugs are discussed as well. Suggestively, OR of CRC cells could significantly be reversed by ferroptosis induction, wherein this result is discussed in the current review. Prospectively, the existing literature discussed in this review will provide a solid foundation for scientists to research the potential use of combined anticancer drugs which can overcome OR via targeting various mechanisms of ferroptosis. Especially, promising therapeutic strategies, challenges ,and opportunities for CRC therapy will be discussed.

摘要

结直肠癌(CRC)对铂类药物可能具有耐药性,可能是通过抑制铁死亡来实现的,但需要进一步的工作来完全理解这一机制。本研究旨在总结与铁稳态相关的奥沙利铂耐药(OR)或耐药性的研究结果,以确定铁死亡调节奥沙利铂作用的潜力。在这篇综述中,讨论了与铁稳态相关的肿瘤发生,包括铁水平确定细胞对铁死亡敏感性、氧化应激或与铁死亡启动相关的结直肠肿瘤细胞中的脂质过氧化,特别是 c-Myc/NRF2 信号通路在调节铁稳态中的作用,以及 NRF2/GPX4 介导的铁死亡。重要的是,铁死亡在 OR 中起关键作用,铁死亡诱导可能显著逆转 CRC 细胞中的 OR,从而抑制奥沙利铂和铁死亡引起的细胞内氧化还原失衡,并导致 CRC 中的化疗耐药。此外,还总结了与 CRC 相关的小分子、铁死亡诱导剂、GPX4 抑制剂或天然产物的 OR 的基础研究及其临床应用。还讨论了小分子或药物的潜在分子靶点和机制。提示,铁死亡诱导可显著逆转 CRC 细胞的 OR,这一结果在本综述中进行了讨论。有前景的是,本综述中讨论的现有文献将为科学家们提供坚实的基础,研究通过靶向铁死亡的各种机制来联合抗癌药物的潜在用途,以克服 OR。特别地,将讨论 CRC 治疗的有前途的治疗策略、挑战和机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a999/10450309/257585b31f73/10.1177_00368504221147173-fig1.jpg

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