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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.
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页码:783 / 797
页数:15
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