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利用膜电位对抗癌症进展。

Harnessing the Membrane Potential to Combat Cancer Progression.

作者信息

Yang Ming, Brackenbury William J

机构信息

York Biomedical Research Institute, Department of Biology, University of York, Heslington, United Kingdom.

出版信息

Bioelectricity. 2022 May 26;4(2):75-80. doi: 10.1089/bioe.2022.0001. eCollection 2022 May.

DOI:10.1089/bioe.2022.0001
PMID:39350772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11441366/
Abstract

Rapid fluctuations in the plasma membrane potential (V) provide the basis underlying the action potential waveform in electrically excitable cells; however, a growing body of literature shows that the V is also functionally instructive in nonexcitable cells, including cancer cells. Various ion channels play a key role in setting and fine tuning the V in cancer and stromal cells within the tumor microenvironment (TME), raising the possibility that the V could be targeted therapeutically using ion channel-modulating compounds. Emerging evidence points to the V as a viable therapeutic target, given its functional significance in regulating cell cycle progression, migration, invasion, immune infiltration, and pH regulation. Several compounds are now undergoing clinical trials and there is increasing interest in therapeutic manipulation of the V via application of pulsed electric fields. The purpose of this article is to update the reader on the significant recent and ongoing progress to elucidate the functional significance of V regulation in tumors, to highlight key remaining questions and the prospect of future therapeutic targeting. In particular, we focus on key developments in understanding the functional consequences of V alteration on tumor development via the activation of small GTPase (K-Ras and Rac1) signaling, as well as the impact of V changes within the heterogeneous TME on immune cell function and cancer progression.

摘要

质膜电位(V)的快速波动为电可兴奋细胞动作电位波形提供了基础;然而,越来越多的文献表明,V在包括癌细胞在内的非可兴奋细胞中也具有功能指导作用。各种离子通道在肿瘤微环境(TME)中的癌细胞和基质细胞中设定和微调V方面起着关键作用,这增加了使用离子通道调节化合物对V进行治疗靶向的可能性。鉴于V在调节细胞周期进程、迁移、侵袭、免疫浸润和pH调节方面的功能意义,新出现的证据表明V是一个可行的治疗靶点。目前有几种化合物正在进行临床试验,并且通过应用脉冲电场对V进行治疗性操纵的兴趣也在增加。本文的目的是向读者介绍最近和正在进行的关于阐明V调节在肿瘤中的功能意义的重大进展,突出仍然存在的关键问题以及未来治疗靶向的前景。特别是,我们关注在理解V改变通过激活小GTP酶(K-Ras和Rac1)信号对肿瘤发展的功能后果方面的关键进展,以及异质性TME内V变化对免疫细胞功能和癌症进展的影响。

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An Ultrasensitive Genetically Encoded Voltage Indicator Uncovers the Electrical Activity of Non-Excitable Cells.一种超灵敏的基因编码电压指示剂揭示了非兴奋细胞的电活动。
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本文引用的文献

1
Monitoring of compound resting membrane potentials of cell cultures with ratiometric genetically encoded voltage indicators.利用比率型基因编码电压指示剂监测细胞培养物的复合静息膜电位。
Commun Biol. 2021 Oct 7;4(1):1164. doi: 10.1038/s42003-021-02675-0.
2
Extracellular K Dampens T Cell Functions: Implications for Immune Suppression in the Tumor Microenvironment.细胞外钾离子抑制T细胞功能:对肿瘤微环境中免疫抑制的影响
Bioelectricity. 2019 Sep 1;1(3):169-179. doi: 10.1089/bioe.2019.0016. Epub 2019 Sep 16.
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Application of Pulsed Electric Fields to Cancer Therapy.脉冲电场在癌症治疗中的应用。
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Substratum stiffness tunes membrane voltage in mammary epithelial cells.基质硬度调节乳腺上皮细胞的膜电压。
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The Interplay between Dysregulated Ion Transport and Mitochondrial Architecture as a Dangerous Liaison in Cancer.离子转运失调与线粒体结构之间的相互作用:癌症中的危险关联
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Increased Interleukin-10 Expression by the Inhibition of Ca-Activated K Channel K3.1 in CD4CD25 Regulatory T Cells in the Recovery Phase in an Inflammatory Bowel Disease Mouse Model.在炎症性肠病小鼠模型的恢复期,通过抑制 CD4CD25 调节性 T 细胞中的钙激活钾通道 K3.1 增加白细胞介素-10 的表达。
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Tumor Treating Fields (TTFields) Hinder Cancer Cell Motility through Regulation of Microtubule and Acting Dynamics.肿瘤治疗电场(TTFields)通过调节微管和肌动蛋白动力学来阻碍癌细胞迁移。
Cancers (Basel). 2020 Oct 17;12(10):3016. doi: 10.3390/cancers12103016.
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Chronic neural activity recorded within breast tumors.乳腺肿瘤内记录的慢性神经活动。
Sci Rep. 2020 Sep 9;10(1):14824. doi: 10.1038/s41598-020-71670-y.
9
Targeting Ion Channels for Cancer Treatment: Current Progress and Future Challenges.靶向离子通道用于癌症治疗:当前进展与未来挑战
Rev Physiol Biochem Pharmacol. 2022;183:1-43. doi: 10.1007/112_2020_46.
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Human Breast Cancer Cells Demonstrate Electrical Excitability.人类乳腺癌细胞表现出电兴奋性。
Front Neurosci. 2020 Apr 30;14:404. doi: 10.3389/fnins.2020.00404. eCollection 2020.