Potassium Channels as a Target for Cancer Therapy: Current Perspectives

被引:33
|
作者
Zuniga, Leandro [1 ,2 ,7 ]
Cayo, Angel [1 ,2 ]
Gonzalez, Wendy [3 ,4 ]
Vilos, Cristian [2 ,5 ,6 ]
Zuniga, Rafael [1 ,2 ]
机构
[1] Univ Talca, Escuela Med, Lab Fisiol Mol, Talca, Chile
[2] Univ Talca, Escuela Med, Ctr Nanomed Diagnost & Desarrollo Farmacos ND3, Talca, Chile
[3] Univ Talca, Ctr Bioinformat & Simulac Mol, Talca, Chile
[4] Univ Talca, Millennium Nucleus Ion Channels Associated Dis MiN, Talca, Chile
[5] Univ Talca, Sch Med, Lab Nanomed & Targeted Delivery, Talca 3460000, Chile
[6] Univ Santiago Chile, Ctr Dev Nanosci & Nanotechnol CEDENNA, Santiago 8350709, Chile
[7] Univ Talca, Escuela Med, Lab Fisiol Mol, Talca 3460000, Chile
来源
ONCOTARGETS AND THERAPY | 2022年 / 15卷
关键词
K+ channels; potassium channel blockers; K+ channels expression; cancer; CA2+-ACTIVATED K+ CHANNEL; PROTEIN-PROTEIN INTERACTIONS; ESTROGEN-RECEPTOR-ALPHA; ION CHANNELS; CELL-PROLIFERATION; UP-REGULATION; HEPATOCELLULAR-CARCINOMA; PROGNOSTIC-SIGNIFICANCE; MITOCHONDRIAL-FUNCTION; CRYSTAL-STRUCTURE;
D O I
10.2147/OTT.S326614
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Potassium (K+) channels are highly regulated membrane proteins that control the potassium ion flux and respond to different cellular stimuli. These ion channels are grouped into three major families, Kv (voltage-gated K+ channel), Kir (inwardly rectifying K+ channel) and K2P (two-pore K+ channels), according to the structure, to mediate the K+ currents. In cancer, alterations in K+ channel function can promote the acquisition of the so-called hallmarks of cancer - cell proliferation, resistance to apoptosis, metabolic changes, angiogenesis, and migratory capabilities - emerging as targets for the development of new therapeutic drugs. In this review, we focus our attention on the different K+ channels associated with the most relevant and prevalent cancer types. We summarize our knowledge about the potassium channels structure and function, their cancer dysregulated expression and discuss the K+ channels modulator and the strategies for designing new drugs.
引用
收藏
页码:783 / 797
页数:15
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