Enam Sahnila, Gan Dai-Di, White Martyn K, Del Valle Luis, Khalili Kamel
Center for Neurovirology, Department of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19122, USA.
Anticancer Res. 2006 Mar-Apr;26(2A):833-41.
Recently, the genome of the human polyomavirus, JC (JCV), and expression of its early and late regulatory proteins (T-antigen and agnoprotein) have been demonstrated in neoplastic cells of colonic cancer cases.
Regulation of JCV was investigated in a human colon cancer cell line (SW480) and compared to a human glioblastoma cell line (U87-MG) that is permissive for JCV replication.
SW480 cells supported basal transcription of both early and late JCV promoters. The expression of TCF-4, a component of Wnt signaling, modulated JCV transcription in a cell type-specific manner. Both TCF-4 and T-antigen bound to the JCV promoter region and bound to each other. In addition, the expression of TCF-4 caused a decrease in the ability of the T-antigen to stimulate viral DNA replication in U87-MG cells.
Wnt pathway signaling proteins and T-antigen interact to regulate JCV in colonic epithelial cells.
最近,已在结肠癌病例的肿瘤细胞中证实了人多瘤病毒JC(JCV)的基因组及其早期和晚期调节蛋白(T抗原和agnoprotein)的表达。
在人结肠癌细胞系(SW480)中研究JCV的调节,并与允许JCV复制的人胶质母细胞瘤细胞系(U87-MG)进行比较。
SW480细胞支持JCV早期和晚期启动子的基础转录。Wnt信号通路的一个组成部分TCF-4的表达以细胞类型特异性方式调节JCV转录。TCF-4和T抗原均与JCV启动子区域结合并相互结合。此外,TCF-4的表达导致T抗原刺激U87-MG细胞中病毒DNA复制的能力下降。
Wnt信号通路信号蛋白与T抗原相互作用以调节结肠上皮细胞中的JCV。