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: UMLS:C0019204 (
hepatocellular carcinoma
)
71,386
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Using a combination of hybridization of PAC to a cDNA library and RACE technique, we isolated a novel cDNA, designated as
C17orf25
(Chromosome 17 open reading frame 25, previously named it HC71A), from the deletion region on chromosome 17p13.3. The cDNA encodes a protein of 313 amino acids with a calculated molecular mass of 34.8 kDa.
C17orf25
is divided into 10 exons and 9 introns, spanning 23 kb of genomic DNA. Northern blot analysis showed that the mRNA expression of
C17orf25
was decreased in
hepatocellular carcinoma
samples as compared to adjacent noncancerous liver tissues from the same patients. The transfection of
C17orf25
into the
hepatocellular carcinoma
cell SMMC7721 and overexpression could inhibit the cell growth. The above results indicate that
C17orf25
is a novel human gene, and the cloning and preliminary characterization of
C17orf25
is a prerequisite for further functional analysis of this novel gene in human
hepatocellular carcinoma
.
...
PMID:Cloning and characterization of a novel gene (C17orf25) from the deletion region on chromosome 17p13.3 in hepatocelular carcinoma. 1164 6
The human
C17orf25
gene (Accession No. AF177342) is one of thirteen genes cloned from a region displaying a high score of loss of heterozygosity within chromosome 17p13.3 in human
hepatocellular carcinoma
in China. To unveil the underlying mechanisms for the transcription regulation of this gene and understand its implication to the hepatocellular carcinogenesis, we looked into the relevant aspects by both bioinformatic and experimental executions. We found: 1, The abundant expression of the
C17orf25
gene was evident in all the cell lines and tissue samples tested, showing little
hepatoma
-selectivity; 2, Its transcription starts at a single site, locating at -60 from the translation initiation codon; 3, A 58 bp fragment containing the transcription start, extending from -112 to -55, represents the minimal promoter; 4, The consensus sequence within this fragment recognized by SP1 contributes predominantly to the activity of the minimal promoter; 5, The bioinformatic analysis suggests that the
C17orf25
gene may encode a protein in the family of the glyoxalase. Our data has provided some deep insight into both function and regulation of the
C17orf25
gene in the context of the normal liver and
hepatocellular carcinoma
.
...
PMID:The promoter analysis of the human C17orf25 gene, a novel chromosome 17p13.3 gene. 1252 92