Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P05231 (
interleukin-6
)
23,907
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The novel human gene
MIA2
encoding a melanoma inhibitory activity (MIA) homologous protein was identified by a GenBank(TM) search.
MIA2
, together with MIA, OTOR, and TANGO, belongs to the novel MIA gene family sharing important structural features, significant homology at both the nucleotide and protein levels, and similar genomic organization. In situ hybridization, reverse transcriptase-PCR, and Northern blots presented a highly tissue-specific
MIA2
expression pattern in the liver. Promoter studies analyzing transcriptional regulation of
MIA2
revealed an HNF-1-binding site at position -236 controlling hepatocyte-specific expression. Mutation of the site led to a complete loss of promoter activity in HepG2 cell. Further sites detected in the
MIA2
promoter were consensus binding sites for SMAD and STAT3, Consistently, stimulation of
MIA2
mRNA expression occurred by treatment with
interleukin-6
, transforming growth factor-beta, and conditioned medium from activated hepatic stellate cells. In accordance with these results,
MIA2
mRNA was found to be increased in liver tissue of patients with chronic hepatitis C infection compared with controls.
MIA2
mRNA levels were significantly higher in patients with severe fibrosis or inflammation than in patients with less severe fibrosis or inflammation. In summary our data indicate that
MIA2
represents a potential novel acute phase protein and
MIA2
expression responds to liver damage. The increased transcription in more severe chronic liver disease suggests that
MIA2
may serve as a marker of hepatic disease activity and severity.
...
PMID:Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. 1258 26