Watanabe, TakaoHiasa, YoichiTokumoto, YoshioHirooka, MasashiAbe, MasanoriIkeda, YoshioMatsuura, BunzoChung, RaymondOnji, Morikazu2014-02-182013Watanabe, Takao, Yoichi Hiasa, Yoshio Tokumoto, Masashi Hirooka, Masanori Abe, Yoshio Ikeda, Bunzo Matsuura, Raymond T. Chung, and Morikazu Onji. 2013. “Protein Kinase R Modulates c-Fos and c-Jun Signaling to Promote Proliferation of Hepatocellular Carcinoma with Hepatitis C Virus Infection.” PLoS ONE 8 (7): e67750. doi:10.1371/journal.pone.0067750. http://dx.doi.org/10.1371/journal.pone.0067750.1932-6203http://nrs.harvard.edu/urn-3:HUL.InstRepos:11717663Double-stranded RNA-activated protein kinase R (PKR) is known to be upregulated by hepatitis C virus (HCV) and overexpressed in hepatocellular carcinoma (HCC). However, the precise roles of PKR in HCC with HCV infection remain unclear. Two HCV replicating cell lines (JFH-1 and H77s), generated by transfection of Huh7.5.1 cells, were used for experiments reported here. PKR expression was modulated with siRNA and a PKR expression plasmid, and cancer-related genes were assessed by real-time PCR and Western blotting; cell lines were further analyzed using a proliferation assay. Modulation of genes by PKR was also assessed in 34 human HCC specimens. Parallel changes in c-Fos and c-Jun gene expression with PKR were observed. Levels of phosphorylated c-Fos and c-Jun were upregulated by an increase of PKR, and were related to levels of phosphorylated JNK1 and Erk1/2. DNA binding activities of c-Fos and c-Jun also correlated with PKR expression, and cell proliferation was dependent on PKR-modulated c-Fos and c-Jun expression. Coordinate expression of c-Jun and PKR was confirmed in human HCC specimens with HCV infection. PKR upregulated c-Fos and c-Jun activities through activation of Erk1/2 and JNK1, respectively. These modulations resulted in HCC cell proliferation with HCV infection. These findings suggest that PKR-related proliferation pathways could be an attractive therapeutic target.en-USBiologyMolecular Cell BiologySignal TransductionSignaling CascadesERK signaling cascadeProtein Kinase Signaling Cascadec-Jun N-terminal kinase signaling cascadeMedicineGastroenterology and HepatologyLiver DiseasesInfectious HepatitisHepatitis CGastrointestinal CancersOncologyCancers and NeoplasmsGastrointestinal TumorsHepatocellular CarcinomaJournal Article2014-02-1810.1371/journal.pone.0067750