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)
Long non-coding RNAs (lncRNAs) have previously been implicated in human disease states, especially cancer. Although the aberrant expression of lncRNAs has been observed in cancer, the biological functions and molecular mechanisms underlying aberrantly expressed lncRNAs in
hepatocellular carcinoma
(
HCC
) have not been widely established. In the present study, we investigated a novel lncRNA, termed URHC (up-regulated in
hepatocellular carcinoma
), and evaluated its role in the progression of
HCC
. Expression profiling using a lncRNA microarray revealed that URHC was highly expressed in 3
HCC
cell lines compared to normal hepatocytes. Quantitative real-time polymerase chain reaction (qRT-PCR) analyses confirmed that URHC expression was increased in
hepatoma
cells and
HCC
tissues. Moreover, using qRT-PCR, we confirmed that URHC expression was up-regulated in 30
HCC
cases (57.7%) and that its higher expression was correlated with poor overall survival. We further demonstrated that URHC inhibition reduced cell proliferation and promoted apoptosis. We hypothesize that URHC may function by regulating the
sterile alpha motif and leucine zipper containing kinase AZK
(ZAK) gene, which is located near URHC on the same chromosome. We found that ZAK mRNA levels were down-regulated in
HCC
tissues and the expression levels of ZAK were negatively correlated with those of URHC in the above
HCC
tissues. Next, we confirmed that URHC down-regulated ZAK, which is involved in URHC-mediated cell proliferation and apoptosis. Furthermore, ERK/MAPK pathway inactivation partially accounted for URHC-ZAK-induced cell growth and apoptosis. Thus, we concluded that high URHC expression can promote cell proliferation and inhibit apoptosis by repressing ZAK expression through inactivation of the ERK/MAPK pathway. These findings may provide a novel mechanism and therapeutic targets for the treatment of
HCC
.
...
PMID:Long non-coding RNA URHC regulates cell proliferation and apoptosis via ZAK through the ERK/MAPK signaling pathway in hepatocellular carcinoma. 2501 76