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抗氧化系统、长链非编码 RNA 和隧道纳米管在细胞死亡救援中的作用。

Antioxidant Systems, lncRNAs, and Tunneling Nanotubes in Cell Death Rescue from Cigarette Smoke Exposure.

机构信息

Disease Molecular Biology and Epigenetics Laboratory, National Institute of Molecular Biology and Biotechnology, University of the Philippines Diliman, Quezon City 1101, Philippines.

出版信息

Cells. 2022 Jul 23;11(15):2277. doi: 10.3390/cells11152277.

Abstract

Cigarette smoke is a rich source of carcinogens and reactive oxygen species (ROS) that can damage macromolecules including DNA. Repair systems can restore DNA integrity. Depending on the duration or intensity of stress signals, cells may utilize various survival and adaptive mechanisms. ROS levels are kept in check through redundant detoxification processes controlled largely by antioxidant systems. This review covers and expands on the mechanisms available to cigarette smoke-exposed cancer cells for restoring the redox balance. These include multiple layers of transcriptional control, each of which is posited to be activated upon reaching a particular stress threshold, among them the pathway, the and pathways, and, finally, , which triggers apoptosis if extreme toxicity is reached. The review also discusses long noncoding RNAs, which have been implicated recently in regulating oxidative stress-with roles in ROS detoxification, the inflammatory response, oxidative stress-induced apoptosis, and mitochondrial oxidative phosphorylation. Lastly, the emerging roles of tunneling nanotubes in providing additional mechanisms for metabolic rescue and the regulation of redox imbalance are considered, further highlighting the expanded redox reset arsenal available to cells.

摘要

香烟烟雾是致癌物质和活性氧(ROS)的丰富来源,这些物质会破坏包括 DNA 在内的大分子。修复系统可以恢复 DNA 完整性。根据应激信号的持续时间或强度,细胞可能会利用各种生存和适应机制。ROS 水平通过主要由抗氧化系统控制的冗余解毒过程得以控制。本篇综述涵盖并扩展了暴露于香烟烟雾的癌细胞用于恢复氧化还原平衡的可用机制。这些机制包括多层次的转录控制,其中每一层都被假定在达到特定的应激阈值时被激活,包括 Nrf2 通路、NF-κB 通路和 MAPK 通路,最终,如果达到极端毒性,会触发细胞凋亡。该综述还讨论了长链非编码 RNA(lncRNA),其最近被认为在调节氧化应激方面发挥作用,包括在 ROS 解毒、炎症反应、氧化应激诱导的细胞凋亡和线粒体氧化磷酸化中的作用。最后,还考虑了隧穿纳米管在提供额外的代谢挽救机制和调节氧化还原失衡方面的新兴作用,这进一步突出了细胞可用的扩展氧化还原重置武器库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a3/9330437/1ba76e88c049/cells-11-02277-g001.jpg

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