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Liver tumor gene expression profile of liver-specific PTEN KO, PTEN/SCAP double KO mice

ABSTRACT: Liver tumor gene expression profile of liver-specific PTEN KO, PTEN/SCAP double KO mice

PROVIDER: PRJNA728674 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR14480588_1.fastq.gz	Fastqsanger.gz
	SRR14480588_2.fastq.gz	Fastqsanger.gz
	SRR14480589_1.fastq.gz	Fastqsanger.gz
	SRR14480589_2.fastq.gz	Fastqsanger.gz
	SRR14480590_1.fastq.gz	Fastqsanger.gz

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Liver gene expression profile of wild type, liver-specific PTEN KO, SCAP KO and PTEN/SCAP double KO mice.

Project description:Nonalcoholic steatohepatitis (NASH), a severe form of nonalcoholic fatty liver disease, is characterized by hepatic steatosis and hepatocellular injury and progresses to cirrhosis and hepatocellular carcinoma. Sterol regulatory element-binding proteins (SREBPs) are master regulators of lipogenesis. Liver-specific PTEN knockout (KO) mice show constitutive upregulation of SREBP through PI3K-Akt pathway activation, leading to spontaneous fatty liver and subsequent HCC development. SREBP cleavage-activating protein (SCAP) plays a critical role in SREBP activation. We sought to determine the impact of SREBP inhibition on NASH and HCC development. To this end, we additionally inhibited SREBP pathway in liver-specific PTEN mice by ablating SCAP and generated liver-specific PTEN/SCAP double KO (DKO) mice. However unexpectedly, inhibition of SCAP/SREBP pathway markedly exacerbated liver injury (5weeks), fibrosis (5months), and carcinogenesis (7 months) in PTEN KO mice. To elucidate the mechanisms of liver injury in liver-specific PTEN/SCAP DKO mice, we conducted transcriptome analyses of the livers.

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