Specific inhibition of the endothelin A receptor with ZD4054: clinical and pre-clinical evidence

被引:84
作者
Morris, CD
Rose, A
Curwen, J
Hughes, AM
Wilson, DJ
Webb, DJ
机构
[1] AstraZeneca, Macclesfield SK10 4TF, Cheshire, England
[2] Univ Edinburgh, Western Gen Hosp, Edinburgh, Midlothian, Scotland
关键词
endothelin A receptor; receptor specificity; cancer; volunteer studies; ZD4054;
D O I
10.1038/sj.bjc.6602676
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Activation of the endothelin A receptor (ETA) by endothelin-1 (ET-1) mediates events that regulate mitogenesis, apoptosis, angiogenesis and metastasis in tumours. Specific blockade of ETA may have anticancer effects, while retaining beneficial endothelin B receptor (ETB)-mediated effects such as apoptosis and clearance of ET-1. ZD4054 is an orally active, specific ETA antagonist in clinical development. In receptor-binding studies, ZD4054 specifically bound to ETA with high affinity; no binding was detected at ETB. In a randomised placebo-controlled trial in eight healthy volunteers, a single oral dose of ZD4054 reduced forearm vasoconstriction in response to brachial artery infusion of ET-1, thus providing clinical evidence of ETA blockade. ETB blockade was assessed in an ascending, single-dose, placebo-controlled trial in 28 volunteers. For all doses of ZD4054, mean plasma ET-1 concentrations measured at 4 and 24 h were within the placebo reference range (a rise in ET-1 would indicate ETB blockade) and there was no evidence of dose-related changes. These data confirm the specificity of ZD4054 for ETA, with no activity at ETB in a clinical or preclinical setting. As a result of this specificity, ZD4054 has the potential to block multiple ETA-induced pathological processes, while allowing beneficial ETB-mediated processes to continue, which may, in turn, lead to an effective cancer therapy.
引用
收藏
页码:2148 / 2152
页数:5
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