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默克尔细胞多瘤病毒在默克尔细胞癌发生中的作用:小T抗原介导c-Jun磷酸化。

Merkel cell polyomavirus in Merkel cell carcinogenesis: small T antigen-mediates c-Jun phosphorylation.

作者信息

Wu Julie H, Simonette Rebecca A, Nguyen Harrison P, Rady Peter L, Tyring Stephen K

机构信息

Department of Dermatology, University of Texas Medical School at Houston, 6431 Fannin Street, Houston, TX, 77030, USA.

Baylor College of Medicine, Houston, TX, 77030, USA.

出版信息

Virus Genes. 2016 Jun;52(3):397-9. doi: 10.1007/s11262-016-1304-3. Epub 2016 Mar 19.

Abstract

Merkel cell carcinoma (MCC) is a highly aggressive neuroendocrine skin cancer associated with the Merkel cell polyomavirus (MCPyV). The MCPyV genome, which is clonally integrated in the majority of MCCs, encodes the regulatory small T (sT) antigen. Previously, reports have established MCPyV sT antigen as a potent oncogene capable of inducing cell transformation. In the current study, we demonstrate a distinct role for c-Jun hyperactivation in MCPyV sT antigen pathogenesis. As MCPyV sT antigen's association with aggressive cancer growth has been previously established, this finding may represent a potential therapeutic target for the treatment of MCCs.

摘要

默克尔细胞癌(MCC)是一种与默克尔细胞多瘤病毒(MCPyV)相关的侵袭性很强的神经内分泌皮肤癌。MCPyV基因组在大多数MCC中呈克隆性整合,编码调节性小T(sT)抗原。此前,有报道称MCPyV sT抗原是一种能够诱导细胞转化的强效癌基因。在本研究中,我们证明了c-Jun过度激活在MCPyV sT抗原发病机制中的独特作用。由于此前已证实MCPyV sT抗原与侵袭性癌症生长有关,这一发现可能代表了治疗MCC的一个潜在治疗靶点。

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