Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2001-6-29
pubmed:abstractText
Polymerase chain reaction (PCR) select complementary DNA (cDNA) subtraction of hepatitis B x antigen (HBxAg)-positive compared with -negative HepG2 cells resulted in the up-regulated expression of a cellular gene that encodes a transcript of 745 bases and a polypeptide 99 amino acids long. GenBank analysis revealed extensive homology with the amino terminal domain of cellular multidrug resistant proteins (MRP), although overexpression of this gene did not confer an MRP phenotype. In situ hybridization and immunostaining showed colocalized expression with HBxAg in the liver of hepatitis B carriers. Overexpression of this protein stimulated the growth of HepG2 cells in serum-free medium, and partially protected cells from anti-Fas-mediated killing, but did not promote growth in soft agar or tumor formation in nude mice. Introduction of the dominant negative inhibitor of nuclear factor kappaB (IkappaBalpha) into HBxAg-positive HepG2 cells decreased the levels of messenger RNA (mRNA) and protein, suggesting that its up-regulation is nuclear factor kappaB (NF-kappaB) dependent. Hence, HBxAg activation of NF-kappaB may result in the up-regulation of a cellular protein that promotes growth factor-independent survival and protects against Fas-mediated killing. This factor may contribute to the persistence of infected hepatocytes during chronic infection, which is important for the later development of hepatocellular carcinoma (HCC).
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0270-9139
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
146-57
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11431746-ATP-Binding Cassette Transporters, pubmed-meshheading:11431746-Amino Acid Sequence, pubmed-meshheading:11431746-Animals, pubmed-meshheading:11431746-Antigens, CD95, pubmed-meshheading:11431746-Base Sequence, pubmed-meshheading:11431746-Blotting, Northern, pubmed-meshheading:11431746-Blotting, Western, pubmed-meshheading:11431746-Carcinoma, Hepatocellular, pubmed-meshheading:11431746-Cell Division, pubmed-meshheading:11431746-Cell Survival, pubmed-meshheading:11431746-Cloning, Molecular, pubmed-meshheading:11431746-DNA, Complementary, pubmed-meshheading:11431746-Drug Resistance, Multiple, pubmed-meshheading:11431746-Gene Expression, pubmed-meshheading:11431746-Gene Expression Regulation, pubmed-meshheading:11431746-Humans, pubmed-meshheading:11431746-In Situ Hybridization, pubmed-meshheading:11431746-Liver Neoplasms, pubmed-meshheading:11431746-Mice, pubmed-meshheading:11431746-Mice, Nude, pubmed-meshheading:11431746-Molecular Sequence Data, pubmed-meshheading:11431746-Multidrug Resistance-Associated Proteins, pubmed-meshheading:11431746-NF-kappa B, pubmed-meshheading:11431746-Polymerase Chain Reaction, pubmed-meshheading:11431746-Proteins, pubmed-meshheading:11431746-RNA, Messenger, pubmed-meshheading:11431746-Sequence Homology, pubmed-meshheading:11431746-Trans-Activators, pubmed-meshheading:11431746-Transfection, pubmed-meshheading:11431746-Tumor Cells, Cultured
pubmed:year
2001
pubmed:articleTitle
A cellular gene up-regulated by hepatitis B virus-encoded X antigen promotes hepatocellular growth and survival.
pubmed:affiliation
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA 19107-6799, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S.