Mouse Gene Set: FUJIWARA_PARK2_HEPATOCYTE_PROLIFERATION_UP

For the Human gene set with the same name, see FUJIWARA_PARK2_HEPATOCYTE_PROLIFERATION_UP

Standard name FUJIWARA_PARK2_HEPATOCYTE_PROLIFERATION_UP
Systematic name MM559
Brief description Genes commonly up-regulated in both non-tumorous and tumorous liver tissues of PARK2 [GeneID=5071] knockout mice.
Full description or abstract The parkin was first identified as a gene implicated in autosomal recessive juvenile Parkinsonism. Deregulation of the parkin gene, however, has been observed in various human cancers, suggesting that the parkin gene may be important in tumorigenesis. To gain insight into the physiologic role of parkin, we generated parkin-/- mice lacking exon 3 of the parkin gene. We demonstrated here that parkin-/- mice had enhanced hepatocyte proliferation and developed macroscopic hepatic tumors with the characteristics of hepatocellular carcinoma. Microarray analyses revealed that parkin deficiency caused the alteration of gene expression profiles in the liver. Among them, endogenous follistatin is commonly upregulated in both nontumorous and tumorous liver tissues of parkin-deficient mice. Parkin deficiency resulted in suppression of caspase activation and rendered hepatocytes resistant to apoptosis in a follistatin-dependent manner. These results suggested that parkin deficiency caused enhanced hepatocyte proliferation and resistance to apoptosis, resulting in hepatic tumor development, partially through the upregulation of endogenous follistatin. The finding that parkin-deficient mice are susceptible to hepatocarcinogenesis provided the first evidence showing that parkin is indeed a tumor suppressor gene.
Collection M2: Curated
      CGP: Chemical and Genetic Perturbations
Source publication Pubmed 18574468   Authors: Fujiwara M,Marusawa H,Wang HQ,Iwai A,Ikeuchi K,Imai Y,Kataoka A,Nukina N,Takahashi R,Chiba T
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Source species Mus musculus
Contributed by Jessica Robertson (MSigDB Team)
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Mouse_RefSeq
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Version history 2022.1.Mm: First Introduced.

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