Chernet Brook, Levin Michael
J Clin Exp Oncol. 2013;Suppl 1. doi: 10.4172/2324-9110.S1-002.
Cancer may be a disease of geometry: a misregulation of the field of information that orchestrates individual cells' activities towards normal anatomy. Recent work identified molecular mechanisms underlying a novel system of developmental control: bioelectric gradients. Endogenous spatio-temporal differences in resting potential of non-neural cells provide instructive cues for cell regulation and complex patterning during embryogenesis and regeneration. It is now appreciated that these cues are an important layer of the dysregulation of cell: cell interactions that leads to cancer. Abnormal depolarization of resting potential (V) is a convenient marker for neoplasia and activates a metastatic phenotype in genetically-normal cells . Moreover, oncogene expression depolarizes cells that form tumor-like structures, but is unable to form tumors if this depolarization is artificially prevented by misexpression of hyperpolarizing ion channels. V triggers metastatic behaviors at considerable distance, mediated by transcriptional and epigenetic effects of electrically-modulated flows of serotonin and butyrate. While data on voltages in carcinogenesis comes mainly from the amphibian model, unbiased genetic screens and network profiling in rodents and human tissues reveal several ion channel proteins as bona fide oncogene and promising targets for cancer drug development. However, we propose that a focus on specific channel genes is just the tip of the iceberg. Bioelectric state is determined by post-translational gating of ion channels, not only from genetically-specified complements of ion translocators. A better model is a statistical dynamics view of spatial V gradients. Cancer may not originate at the single cell level, since gap junctional coupling results in multi-cellular physiological networks with multiple stable attractors in bioelectrical state space. New medical applications await a detailed understanding of the mechanisms by which organ target morphology stored in real-time patterns of ion flows is perceived or mis-perceived by cells. Mastery of somatic voltage gradients will lead to cancer normalization or rebooting strategies, such as those that occur in regenerating and embryonic organs, resulting in transformative advances in basic biology and oncology.
一种信息场的失调,该信息场协调单个细胞的活动以形成正常解剖结构。最近的研究确定了一种新型发育控制系统——生物电梯度——背后的分子机制。非神经细胞静息电位的内源性时空差异为胚胎发育和再生过程中的细胞调节和复杂模式形成提供了指导性线索。现在人们认识到,这些线索是导致癌症的细胞间相互作用失调的重要层面。静息电位(V)的异常去极化是肿瘤形成的一个便捷标志物,并在基因正常的细胞中激活转移表型。此外,癌基因表达会使形成肿瘤样结构的细胞去极化,但如果通过超极化离子通道的错误表达人为地阻止这种去极化,这些细胞就无法形成肿瘤。V在相当远的距离触发转移行为,这是由血清素和丁酸盐电调制流动的转录和表观遗传效应介导的。虽然关于致癌过程中电压的数据主要来自两栖动物模型,但在啮齿动物和人体组织中进行的无偏遗传筛选和网络分析揭示了几种离子通道蛋白是真正的癌基因,也是癌症药物开发的有前景的靶点。然而,我们认为专注于特定的通道基因只是冰山一角。生物电状态是由离子通道的翻译后门控决定的,而不仅仅取决于离子转运体的基因指定互补物。一个更好的模型是空间V梯度的统计动力学观点。癌症可能并非起源于单细胞水平,因为间隙连接耦合会导致生物电状态空间中具有多个稳定吸引子的多细胞生理网络。新的医学应用等待着对细胞感知或错误感知以离子流实时模式存储的器官靶形态的机制有详细的了解。掌握体细胞电压梯度将导致癌症正常化或重启策略,就像在再生和胚胎器官中发生的那些策略一样,从而在基础生物学和肿瘤学方面带来变革性进展。