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)
Recent studies report that microRNA-519a (miR-519a) is a novel oncomir, which facilitates the onset and progression of human cancers. However, the clinical significance of miR-519a and its functional role and underlying mechanisms in
hepatocellular carcinoma
(
HCC
) are poorly investigated. In the present study, elevated expression of miR-519a was observed in
HCC
tissues compared with adjacent non-tumor tissues. The increased level of miR-519a expression was significantly correlated with adverse clinical features of
HCC
including hepatitis B virus (HBV) infection, large tumor size, cirrhosis and advanced tumor-node-metastasis tumor stage. Furthermore, high expression of miR-519a was prominently associated with a poorer 5-year overall survival and recurrence-free survival of
HCC
patients. Gain- and loss-of function experiments showed that miR-519a overexpression enhanced proliferation and reduced apoptosis of Huh7 cells. By contrast, miR-519a knockdown inhibited SMMC-7721 cell proliferation and induced apoptosis. Importantly, up-regulation of miR-519a reduced the expression of
FOXF2
mRNA and protein in Huh7 cells, while down-regulation of miR-519a resulted in increased expression of
FOXF2
in SMMC-7721 cells. An inverse correlation between mRNA levels of miR-519a and
FOXF2
was observed in
HCC
tissues. Thus,
Forkhead box F2
(
FOXF2
) was identified as a downstream target of miR-519a in
HCC
. Mechanistically, the effects of miR-519a knockdown on SMMC-7721 cells were abrogated by
FOXF2
repression. In conclusion, miR-519a is a novel prognostic predictor for
HCC
patients and it may potentiate proliferation and inhibits apoptosis of
HCC
cells by targeting
FOXF2
.
...
PMID:MicroRNA-519a promotes proliferation and inhibits apoptosis of hepatocellular carcinoma cells by targeting FOXF2. 2669 96