2021
DOI: 10.1089/bioe.2020.0051
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Clinical Potential of Nerve Input to Tumors: A Bioelectricity Perspective

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Cited by 5 publications
(4 citation statements)
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“…Optogenetics research can inspire the development of novel closed-loop neurostimulation systems [ 225 ]. By combining optogenetic techniques with responsive neurostimulation technologies, it may be possible to create closed-loop systems that detect aberrant neural activity and deliver precisely timed light stimulation to prevent or disrupt seizure activity [ 130 , 226 ]. This hybrid approach could potentially offer a personalized and adaptive therapy for individuals with drug-resistant epilepsy.…”
Section: Optogenetics In Epilepsy Researchmentioning
confidence: 99%
“…Optogenetics research can inspire the development of novel closed-loop neurostimulation systems [ 225 ]. By combining optogenetic techniques with responsive neurostimulation technologies, it may be possible to create closed-loop systems that detect aberrant neural activity and deliver precisely timed light stimulation to prevent or disrupt seizure activity [ 130 , 226 ]. This hybrid approach could potentially offer a personalized and adaptive therapy for individuals with drug-resistant epilepsy.…”
Section: Optogenetics In Epilepsy Researchmentioning
confidence: 99%
“…In chemogenetics, genetically modified cells are engineered to express designer receptors exclusively activated by designer drugs (DREADDs). For example, neurons with mutant G-protein-coupled muscarinic acetylcholine receptors respond to the synthetic drug clozapine-N-oxide (CNO) instead of acetylcholine [ 114 , 115 , 116 ]. A G q -coupled DREADD (hM3Dq) can be used to enhance neuronal activity, whereas another G i/o -coupled DREADD (hM4Di) may inhibit neuronal activity [ 116 ].…”
Section: Review Of the Literaturementioning
confidence: 99%
“…In this line, CNO, an already accepted and administered compound with no significant side effects in humans, could be used to control cancer. For the application of chemogenetics in human cancer, the selection of the desired neuronal groups (e.g., those involved in stress response) or cancer cells (that are to be directly targeted), genetic manipulation of the exact receptor and ligand combinations, and definition of the proper timing will all be essential [ 114 , 115 ]. While in a very early stage of development, this receptor-specific approach has a great potential for future implementation in precision oncology.…”
Section: Review Of the Literaturementioning
confidence: 99%
“…Not only is it crucial to characterize the cancer cells themselves, but also the tumor microenvironment (TME). The TME includes the non-tumor cells, extracellular matrix, and local microbiota [2], as well as the biochemical, biophysical [3], and bioelectric conditions of the stroma and interstitial fluid that exist in and around a tumor [4,5]. Our basic understanding of the PDAC TME is rapidly evolving, and a combination of experimental and observational evidence indicates that the TME affects clinical outcomes in PDAC by influencing its outgrowth and responses to therapy [6,7].…”
Section: Introductionmentioning
confidence: 99%