中文摘要：

目的: 鞘氨醇 kinase (SPHK1 ) 1 涉及各种各样的细胞的函数包括房间生长，移植， apoptosis，细胞骨架体系结构和钙 homoeostasis，等等。作为 oncogenic kinase， SPHK1 与癌症的发展和前进被联系。这研究的目的是调查 SPHK1 是否涉及肝炎 B 病毒 X 蛋白质(HBx ) 导致的 hepatocarcinogenesis。

英文摘要：

Aim： Sphingosine kinase 1 （SPHK1） is involved in various cellular functions, including cell growth, migration, apoptosis, cytoskeleton architecture and calcium homoeostasis, etc. As an oncogenic kinase, SPHK1 is associated with the development and progression of cancers. The aim of this study was to investigate whether SPHK1 was involved in hepatocarcinogenesis induced by the hepatitis B virus X protein （HBx）. Methods： The expression of SPHK1 in hepatocellular carcinoma （HCC） tissue and hepatoma cells were measured using qRT-PCR and Western blot analysis. HBx expression levels in hepatoma cells were modulated by transiently transfected with HBx or psi-HBx plasmids. The SPHK1 promoter activity was measured using luciferase reporter gene assay, and the interaction of the transcription factor AP2α with the SPHK1 promoter was studied with chromatin immunoprecipitation assay. The growth of hepatoma cells was evaluated in vitro using MTT and colony formation assays, and in a tumor xenograft model.Results： A positive correlation was found between the mRNA levels of SPHK1 and HBx in 38 clinical HCC samples （r=＋0.727, P〈0.01）. Moreover, the expression of SPHK1 was markedly increased in the liver cancer tissue of HBx-transgenic mice. Overexpressing HBx in normal liver cells LO2 and hepatoma cells HepG2 dose-dependently increased the expression of SPHK1, whereas silencing HBx in HBx-expressing hepatoma cells HepG2-X and HepG2.2.15 suppressed SPHK1 expression. Furthermore, overexpressing HBx in HepG2 cells dose-dependently increased the SPHK1 promoter activity, whereas silencing HBx in HepG2-X cells suppressed this activity. In HepG2-X cells, AP2α was found to directly interact with the SPHK1 promoter, and silencing AP2α suppressed the SPHK1 promoter activity and SPHK1 expression. Silencing HBx in HepG2-X cells abolished the HBx-enhanced proliferation and colony formation in vitro, and tumor growth in vivo.Conclusion： HBx upregulates SPHK1 through the transcription factor AP2α, which promotes