可药性
线粒体
背景(考古学)
生物
计算生物学
粒线体疾病
钾通道
神经科学
离子通道
疾病
生物信息学
线粒体融合
医学
线粒体DNA
细胞生物学
遗传学
病理
基因
古生物学
生物物理学
受体
作者
Vanessa Checchetto,Luigi Leanza,Diego De Stefani,Rosario Rizzuto,Erich Gulbins,Ildikò Szabó
标识
DOI:10.1016/j.pharmthera.2021.107874
摘要
The field of mitochondrial ion channels underwent a rapid development during the last decade, thanks to the molecular identification of some of the nuclear-encoded organelle channels and to advances in strategies allowing specific pharmacological targeting of these proteins. Thereby, genetic tools and specific drugs aided definition of the relevance of several mitochondrial channels both in physiological as well as pathological conditions. Unfortunately, in the case of mitochondrial K+ channels, efforts of genetic manipulation provided only limited results, due to their dual localization to mitochondria and to plasma membrane in most cases. Although the impact of mitochondrial K+ channels on human diseases is still far from being genuinely understood, pre-clinical data strongly argue for their substantial role in the context of several pathologies, including cardiovascular and neurodegenerative diseases as well as cancer. Importantly, these channels are druggable targets, and their in-depth investigation could thus pave the way to the development of innovative small molecules with huge therapeutic potential. In the present review we summarize the available experimental evidence that mechanistically link mitochondrial potassium channels to the above pathologies and underline the possibility of exploiting them for therapy.
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