Literature DB >> 9192090

dl-propranolol negatively regulates the transcription of proliferating cell nuclear antigen (PCNA)-gene and thereby suppresses DNA synthesis in regenerating rat liver.

J H Hong1, E S Hwang, C H Lee, Y H Lee, S K Lee.   

Abstract

Previous reports have suggested that dl-propranolol (PRL) suppresses DNA synthesis by blocking cAMP-mediated signaling in rat liver after partial hepatectomy (PH). Here, we examined if PRL negatively regulates the expression of genes involved in cell cycle progression. Immunoblotting assays showed that the protein levels of cyclins A and E, Cdk2, p21WAF1, and p27KIP1 did not significantly change in liver tissues from either vehicle- or PRL-injected rats after PH. However, the levels of PCNA and PCNA-mRNA markedly decreased in the remnant liver in response to PRL-injection. Similarly, PCNA-CRE binding activity of nuclear 43kDa CREB was suppressed, although the protein levels were not altered. We suggest that PRL negatively regulates the PCNA-gene transcription by interfering with the cAMP/PKA-mediated induction of CREB binding to the CRE-sequences and thereby suppresses DNA synthesis in regenerating rat liver.

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Year:  1997        PMID: 9192090     DOI: 10.1080/15216549700202481

Source DB:  PubMed          Journal:  Biochem Mol Biol Int        ISSN: 1039-9712


  1 in total

1.  Functional integration of hepatocytes derived from human mesenchymal stem cells into mouse livers.

Authors:  Ines Aurich; Lutz P Mueller; Hendryk Aurich; Jana Luetzkendorf; Kai Tisljar; Matthias M Dollinger; Wiebke Schormann; Jens Walldorf; Jan G Hengstler; Wolfgang E Fleig; Bruno Christ
Journal:  Gut       Date:  2006-08-23       Impact factor: 23.059

  1 in total

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