| First Author | Tian Y | Year | 2016 |
| Journal | Glycoconj J | Volume | 33 |
| Issue | 6 | Pages | 927-936 |
| PubMed ID | 27318478 | Mgi Jnum | J:320870 |
| Mgi Id | MGI:6880818 | Doi | 10.1007/s10719-016-9703-1 |
| Citation | Tian Y, et al. (2016) Age-dependent PPARalpha activation induces hepatic sulfatide accumulation in transgenic mice carrying the hepatitis C virus core gene. Glycoconj J 33(6):927-936 |
| abstractText | Sulfatides, a type of glycosphingolipid, are associated with carcinogenesis. Peroxisome proliferator-activated receptor alpha (PPARalpha) is involved in the regulation of sulfatide metabolism as well as in cancer development. We previously reported that transgenic (Tg) mice expressing hepatitis C virus core protein (HCVcp) exhibited age-dependent PPARalpha activation and carcinogenesis in liver. However, the metabolism of sulfatides in hepatocellular carcinoma is unknown. To examine the relationship between sulfatide metabolism, carcinogenesis, HCVcp, and PPARalpha, age-dependent changes of these factors were examined in HCVcpTg, PPARalpha inhibitor-treated HCVcpTg, and non-Tg mice. The sulfatide content in liver, the hepatic expression of two key enzymes catalyzing the initial and last reactions in sulfatide synthesis, the hepatic expression of known sulfatide-transferring protein, oxidative stress, and hepatic PPARalpha expression and its activation were age-dependently increased in HCVcpTg mice. The increased synthesis and accumulation of sulfatides and PPARalpha activation were significantly enhanced in liver cancer lesions. These changes were attenuated by PPARalpha inhibitor treatment and not observed in non-Tg mice. These results suggest that HCVcp-induced age-dependent PPARalpha activation increases synthesis of sulfatides and the resulting sulfatide accumulation affects HCV-related liver cancer. The monitoring of hepatic sulfatide content and the modulation of sulfatide generation by intervention using a PPARalpha inhibitor might be useful for the prediction and prevention of HCV-related hepatocarcinogenesis, respectively. |
