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细胞周期蛋白依赖性激酶作为开发新型抗病毒治疗药物的新兴靶点。

Cyclin-dependent Kinases as Emerging Targets for Developing Novel Antiviral Therapeutics.

机构信息

AIDS Research Institute-IrsiCaixa and Health Research Institute Germans Trias i Pujol (IGTP), Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, 08916, Badalona, Spain.

AIDS Research Institute-IrsiCaixa and Health Research Institute Germans Trias i Pujol (IGTP), Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, 08916, Badalona, Spain; B-ARGO (Badalona Applied Research Group in Oncology) and Health Research Institute Germans Trias i Pujol (IGTP), ICO-Badalona, Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, 08916, Badalona, Spain.

出版信息

Trends Microbiol. 2021 Sep;29(9):836-848. doi: 10.1016/j.tim.2021.01.014. Epub 2021 Feb 19.

Abstract

Besides its prominent role in cell proliferation, cyclin-dependent kinases (CDKs) are key players in viral infections as both DNA and RNA viruses modify CDK function to favor viral replication. Recently, a number of specific pharmacological CDK inhibitors have been developed and approved for cancer treatment. The repurposing of these specific CDK inhibitors for the treatment of viral infections may represent a novel effective therapeutic strategy to combat old and emergent viruses. In this review, we describe the role, mechanisms of action, and potential of CDKs as antiviral drug targets. We also discuss the current clinical state of novel specific CDK inhibitors, focusing on their putative use as antivirals, especially against new emerging viruses.

摘要

除了在细胞增殖中发挥突出作用外,细胞周期蛋白依赖性激酶(CDKs)也是病毒感染的关键因素,因为 DNA 和 RNA 病毒都会改变 CDK 的功能以促进病毒复制。最近,已经开发出许多特定的细胞周期蛋白依赖性激酶抑制剂并批准用于癌症治疗。将这些特定的细胞周期蛋白依赖性激酶抑制剂重新用于治疗病毒感染可能代表一种对抗旧病毒和新兴病毒的新型有效治疗策略。在这篇综述中,我们描述了 CDK 作为抗病毒药物靶点的作用、作用机制和潜力。我们还讨论了新型特定 CDK 抑制剂的当前临床状态,重点讨论了它们作为抗病毒药物的潜在用途,特别是针对新出现的病毒。

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