Transient Receptor Potential Canonical (TRPC) Channels as Modulators of Migration and Invasion

被引:33
作者
Asghar, Muhammad Yasir [1 ,2 ]
Tornquist, Kid [1 ,2 ]
机构
[1] Biomedicum Helsinki 2U, Minerva Fdn Inst Med Res, Tukholmankatu 8, Helsinki 00290, Finland
[2] Abo Akad Univ, Fac Sci & Engn, Tykistokatu 6A, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
TRPC; ion channels; cancer; thyroid; calcium; migration; invasion; angiogenesis; CA2+ ENTRY; CELL-PROLIFERATION; ION CHANNELS; ENDOTHELIAL-CELLS; EPITHELIAL-CELLS; IN-VITRO; CALCIUM; STORE; CANCER; EXPRESSION;
D O I
10.3390/ijms21051739
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calcium (Ca2+) is perhaps the most versatile signaling molecule in cells. Ca2+ regulates a large number of key events in cells, ranging from gene transcription, motility, and contraction, to energy production and channel gating. To accomplish all these different functions, a multitude of channels, pumps, and transporters are necessary. A group of channels participating in these processes is the transient receptor potential (TRP) family of cation channels. These channels are divided into 29 subfamilies, and are differentially expressed in man, rodents, worms, and flies. One of these subfamilies is the transient receptor potential canonical (TRPC) family of channels. This ion channel family comprises of seven isoforms, labeled TRPC1-7. In man, six functional forms are expressed (TRPC1, TRPC3-7), whereas TRPC2 is a pseudogene; thus, not functionally expressed. In this review, we will describe the importance of the TRPC channels and their interacting molecular partners in the etiology of cancer, particularly in regard to regulating migration and invasion.
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页数:15
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