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沙卡替尼抑制体外中东呼吸综合征冠状病毒复制。

Saracatinib Inhibits Middle East Respiratory Syndrome-Coronavirus Replication In Vitro.

机构信息

Virus Research Group, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea.

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea.

出版信息

Viruses. 2018 May 24;10(6):283. doi: 10.3390/v10060283.

DOI:10.3390/v10060283
PMID:29795047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6024778/
Abstract

The Middle East respiratory syndrome-coronavirus (MERS-CoV), first identified in Saudi Arabia, is an emerging zoonotic pathogen that causes severe acute respiratory illness in humans with a high fatality rate. Since its emergence, MERS-CoV continues to spread to countries outside of the Arabian Peninsula and gives rise to sporadic human infections following the entry of infected individuals to other countries, which can precipitate outbreaks similar to the one that occurred in South Korea in 2015. Current therapeutics against MERS-CoV infection have primarily been adapted from previous drugs used for the treatment of severe acute respiratory syndrome. In search of new potential drug candidates, we screened a library composed of 2334 clinically approved drugs and pharmacologically active compounds. The drug saracatinib, a potent inhibitor of Src-family of tyrosine kinases (SFK), was identified as an inhibitor of MERS-CoV replication in vitro. Our results suggest that saracatinib potently inhibits MERS-CoV at the early stages of the viral life cycle in Huh-7 cells, possibly through the suppression of SFK signaling pathways. Furthermore, saracatinib exhibited a synergistic effect with gemcitabine, an anticancer drug with antiviral activity against several RNA viruses. These data indicate that saracatinib alone or in combination with gemcitabine can provide a new therapeutic option for the treatment of MERS-CoV infection.

摘要

中东呼吸综合征冠状病毒(MERS-CoV)最初在沙特阿拉伯被发现,是一种新兴的人畜共患病原体,可导致人类发生严重急性呼吸道疾病,病死率较高。自出现以来,MERS-CoV 继续传播到阿拉伯半岛以外的国家,并在感染个体进入其他国家后引发散发性人类感染,这可能会引发类似于 2015 年在韩国发生的疫情。目前针对 MERS-CoV 感染的治疗方法主要是从以前用于治疗严重急性呼吸综合征的药物中改编而来。为了寻找新的潜在药物候选物,我们筛选了一个由 2334 种临床批准的药物和具有药理活性的化合物组成的文库。药物 saracatinib 是一种Src 家族酪氨酸激酶(SFK)的强效抑制剂,被鉴定为体外抑制 MERS-CoV 复制的抑制剂。我们的研究结果表明,saracatinib 在 Huh-7 细胞中病毒生命周期的早期阶段强烈抑制 MERS-CoV,可能是通过抑制 SFK 信号通路。此外,saracatinib 与吉西他滨表现出协同作用,吉西他滨是一种具有抗病毒活性的抗癌药物,可对抗几种 RNA 病毒。这些数据表明,saracatinib 单独或与 gemcitabine 联合使用可为治疗 MERS-CoV 感染提供新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/ecce0c84dc75/viruses-10-00283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/25ee8f9a7d35/viruses-10-00283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/319c394d3574/viruses-10-00283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/d82ebf1ff058/viruses-10-00283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/c0a6b1a2a7c4/viruses-10-00283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/8b62ac4372b7/viruses-10-00283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/ecce0c84dc75/viruses-10-00283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/25ee8f9a7d35/viruses-10-00283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/319c394d3574/viruses-10-00283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/d82ebf1ff058/viruses-10-00283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/c0a6b1a2a7c4/viruses-10-00283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/8b62ac4372b7/viruses-10-00283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/6024778/ecce0c84dc75/viruses-10-00283-g006.jpg

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