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离子通道和神经递质调节剂作为电疗控制癌症的方法。

Ion Channel and Neurotransmitter Modulators as Electroceutical Approaches to the Control of Cancer.

机构信息

Department of Oncology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta. Canada.

Laboratory of Biological System Modeling, National Institute for Science and Technology on Innovation in Neglected Diseases (INCT/IDN), Center for Technological Development in Health (CDTS), Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro. Brazil.

出版信息

Curr Pharm Des. 2017;23(32):4827-4841. doi: 10.2174/1381612823666170530105837.

Abstract

The activities of individual cells must be tightly coordinated in order to build and maintain complex 3- dimensional body structures during embryogenesis and regeneration. Thus, one way to view cancer is within systems biology as a network disorder affecting the ability of cells to properly interact with a morphodynamic field of instructive signals that keeps proliferation and migration orchestrated toward the anatomical needs of the host organism. One layer of this set of instructive microenvironmental cues is bioelectrical. Voltage gradients among all somatic cells (not just excitable nerve and muscle) control cell behavior, and the ionic coupling of cells into networks via electrochemical synapses allows them to implement tissue-level patterning decisions. These gradients have been increasingly implicated in the induction and suppression of tumorigenesis and metastasis, in the emerging links between developmental bioelectricity to the cancer problem. Consistent with the well-known role of neurotransmitter molecules in transducing electrical activity to downstream cascades in the brain, serotonergic signaling has likewise been implicated in cancer. Here, we review these recent data and propose new approaches for manipulating bioelectric and neurotransmitter pathways in cancer biology based on a bioelectric view of cancer. To support this methodology, we present new data on the effects of the SSRI Prozac and its analog (ZINC ID = ZINC06811610) on survival of both cancer (MCF7) and normal (MCF10A) breast cells exposed to these compounds. We found an IC50 concentration (25 µM for Prozac and 100 µM for the Prozac analog) at which these compounds inhibited tumor cell survival and proliferation. Additionally, at these concentrations, we did not observe alterations in a non-tumoral cell line. This constitutes a proof-of-concept demonstration for our hypothesis that the use of both existing and novel drugs as electroceuticals could serve as an alternative to highly toxic chemotherapy strategies replacing or augmenting them with less toxic alternatives. We believe this new approach forms an exciting roadmap for future biomedical advances.

摘要

为了在胚胎发生和再生过程中构建和维持复杂的三维身体结构,个体细胞的活动必须紧密协调。因此,从系统生物学的角度来看,癌症可以被视为一种网络紊乱,影响细胞与形态动力场中指令信号正确相互作用的能力,这些信号保持增殖和迁移协调,以满足宿主生物体的解剖需求。这套指令性微观环境线索的一层是生物电的。所有体细胞(不仅仅是可兴奋的神经和肌肉)之间的电压梯度控制着细胞的行为,而细胞通过电化学突触耦合成网络,使它们能够实施组织水平的模式决策。这些梯度越来越多地参与了肿瘤发生和转移的诱导和抑制,以及发育生物电与癌症问题之间新兴联系。与神经递质分子在将电活动转导到大脑下游级联中的已知作用一致,5-羟色胺信号也与癌症有关。在这里,我们回顾了这些最近的数据,并根据癌症的生物电观点提出了新的方法来操纵生物电和神经递质途径在癌症生物学中的作用。为了支持这种方法,我们提出了新的数据,表明 SSRI 百忧解及其类似物(ZINC ID = ZINC06811610)对暴露于这些化合物的癌细胞(MCF7)和正常细胞(MCF10A)的存活的影响。我们发现了一个 IC50 浓度(百忧解为 25µM,百忧解类似物为 100µM),在该浓度下,这些化合物抑制了肿瘤细胞的存活和增殖。此外,在这些浓度下,我们没有观察到非肿瘤细胞系的变化。这构成了我们假设的概念验证,即使用现有的和新型药物作为电疗可以作为高度有毒的化疗策略的替代方案,用毒性较小的替代方案替代或增强它们。我们相信这种新方法为未来的生物医学进步提供了一个令人兴奋的路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/6340161/6f3768345829/CPD-23-4827_F1.jpg

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