Anti-tumour/metastasis effects of the potassium-sparing diuretic amiloride: an orally active anti-cancer drug waiting for its call-of-duty?

被引:86
作者
Matthews, Hayden [1 ]
Ranson, Marie [2 ,3 ]
Kelso, Michael J. [1 ]
机构
[1] Univ Wollongong, Sch Chem, Wollongong, NSW 2522, Australia
[2] Univ Wollongong, Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia
[3] Univ Wollongong, Sch Biol Sci, Wollongong, NSW 2522, Australia
关键词
amiloride; metastasis; anti-metastasis drug; chemotherapy; NHE; plasminogen activation system; uPA; UROKINASE PLASMINOGEN-ACTIVATOR; COLON-CANCER CELLS; TUMOR-NECROSIS-FACTOR; SENSING ION CHANNELS; H+ EXCHANGER NHE1; NA+/H+ EXCHANGER; INTRACELLULAR PH; BREAST-CANCER; EXTRACELLULAR PH; PROSTATE-CANCER;
D O I
10.1002/ijc.26156
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Amiloride.HCl is clinically used as an oral potassium-sparing diuretic, but multiple studies in biochemical, cellular and animal models have shown that the drug also possesses anti-tumour and anti-metastasis activities. The additional effects appear to arise through inhibition of two discrete targets: (i) the sodium-hydrogen exchanger 1 (NHE1), a membrane protein responsible for the characteristically low extracellular pH of tumours and (ii) the urokinase-type plasminogen activator (uPA), a serine protease mediator of cell migration, invasion and metastasis and well-known marker of poor prognosis in cancer. This mini-review summarises for the first time the reported anti-tumour/metastasis effects of amiloride in experimental models, discusses the putative molecular mechanisms responsible for these effects and concludes by commenting on the pros and cons of trialling amiloride or one of its structural analogues as potential new anti-tumour/metastasis drugs.
引用
收藏
页码:2051 / 2061
页数:11
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