Wu Julie H, Simonette Rebecca A, Nguyen Harrison P, Rady Peter L, Tyring Stephen K
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.
Virus Genes. 2016 Jun;52(3):397-9. doi: 10.1007/s11262-016-1304-3. Epub 2016 Mar 19.
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.
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。