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: EC:2.7.13.3 (
histidine kinase
)
2,405
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Hepatocellular carcinoma
(
HCC
) is known as a frequent type of primary cancer in the liver, and it is the third-most common cause of cancer-related death all over the world. However, the molecular mechanism in the progression of
HCC
is still unclear. The current study was designed to investigate the expression and function of microRNA-34a (miR-34a) in
HCC
. In
HCC
tissues and cells, the expression levels of miR-34a were analyzed by quantitative real-time polymerase chain reaction. The association between the level of miR-34a and hexokinase (HK)-1 was also investigated via luciferase reporter assay. Cell viability and proliferation were detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and flow cytometry. To assess whether miR-34a can limit tumor growth in vivo, animal models and terminal deoxynucleotidyl transferase dUTP nick end labeling assay were used for examining the role of miR-34a on the development of
HCC
and cell apoptosis. The expression level of miR-34a was reduced in
HCC
samples and cells. The expression of miR-34a was associated with the viability and proliferation capacity of
HCC
cells, and miR-34a could inhibit
HCC
cells proliferation by inhibiting
HK1
. In the mouse model of
HCC
, volumes and weight of the tumors were significantly decreased by transfection with miR-34a mimic compared with the control group. Furthermore, miR-34a mimics could induce apoptosis in a greater proportion of cells compared with the control group. Taken together, the data may provide some novel insights into the molecular mechanism of miR-34a and
HK1
in the progression of
HCC
. Thus, miR-34a/
HK1
axis might be a novel promising therapeutic target for treating
HCC
.
...
PMID:MicroRNA-34a inhibit hepatocellular carcinoma progression by repressing hexokinase-1. 3047 1