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首页> 外文期刊>BioMed research international >Comparison of FDA Approved Kinase Targets to Clinical Trial Ones: Insights from Their System Profiles and Drug-Target Interaction Networks
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Comparison of FDA Approved Kinase Targets to Clinical Trial Ones: Insights from Their System Profiles and Drug-Target Interaction Networks

机译:FDA批准的激酶目标对临床试验的比较:他们的系统简介和药物 - 目标交互网络见解

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摘要

Kinase is one of the most productive classes of established targets, but the majority of approved drugs against kinase were developed only for cancer. Intensive efforts were therefore exerted for releasing its therapeutic potential by discovering new therapeutic area. Kinases in clinical trial could provide great opportunities for treating various diseases. However, no systematic comparison between system profiles of established targets and those of clinical trial ones was conducted. The reveal of probable difference or shift of trend would help to identify key factors defining druggability of established targets. In this study, a comparative analysis of system profiles of both types of targets was conducted. Consequently, the systems profiles of the majority of clinical trial kinases were identified to be very similar to those of established ones, but percentages of established targets obeying the system profiles appeared to be slightly but consistently higher than those of clinical trial targets. Moreover, a shift of trend in the system profiles from the clinical trial to the established targets was identified, and popular kinase targets were discovered. In sum, this comparative study may help to facilitate the identification of the druggability of established drug targets by their system profiles and drug-target interaction networks.
机译:激酶是既定目标最有效的阶级之一,但大多数对激酶的批准药物仅用于癌症。因此,通过发现新的治疗区域施加密集努力来释放其治疗潜力。临床试验中的激酶可以为治疗各种疾病提供巨大的机会。然而,进行了既定目标的系统概况和临床试验者的系统概况之间没有系统的比较。揭示可能的差异或转变趋势将有助于确定定义既定目标可脱毒性的关键因素。在该研究中,进行了两种类型目标的系统谱的比较分析。因此,鉴定了大多数临床试验激酶的系统谱与成熟的临床试验激酶非常相似,但遵守系统曲线的既定目标百分比似乎略微但持续高于临床试验目标。此外,鉴定了从临床试验到已建立的靶标的系统谱的趋势转变,并且发现了流行的激酶靶标。总之,这种比较研究可以有助于促进其系统谱和药物目标相互作用网络的已建立的药物靶标的可用性。

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