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1.
Organ Transplantation ; (6): 152-156, 2015.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-731580

ABSTRACT

Objective To discuss the effect of G-protein-coupled receptor 49 (GPR49)gene on proliferation and invasive ability of hepatoma cell line Huh7 and its molecular biological mechanism.Methods According to the different transfected small interfering RNA(si-RNA),Huh7 cells were divided into the GPR49-siRNA(si-GPR49)group and the NC-siRNA (si-NC)group.Untransfected Huh7 cells were set as the control group. Messenger RNA (mRNA )and protein expression of GPR49, cyclin D1 and matrix metalloproteinase 9 (MMP9)in the cells of the three groups were respectively detected by reverse transcription-polymerase chain reaction (RT-PCR)and Western blot method.The proliferation and invasive ability of the cells of each group were respectively detected by MTT method and Transwell method.Results The relative expression of GPR49 mRNA of the si-GPR49 group was (23.8 ±3.1)% of the control group (P <0.05). Compared with the control group,the protein expression of GPR49,cyclin D1 and MMP9 of the si-GPR49 group decreased significantly (all in P <0.05).The proliferation experiment results by MTT indicated that the optical density(OD)of the cells of the si-GPR49 group at 72 h was (0.53 ±0.12),which was significantly lower than that of the control group (1.35 ±0.28).The difference had statistical significance (P <0.05). The average invaded cell counts of the si-GPR49 group were (13.6 ±2.5),which was significantly lower than (65.3 ±6.1 )of the control group.The difference had statistical significance (P <0.05 ).Conclusions GPR49-siRNA may inhibit the gene expression of GPR49 in Huh7 cells.Its mechanism may be that the proliferation of Huh7 cells is inhibited by reducing the level of cyclin D1;the migration and invasive ability of Huh7 cells is inhibited by affecting the expression level of MMP9.

2.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-599416

ABSTRACT

Objective To discuss the relationship between the abdominal microenvironment with abdominal cavity metastasis of epithelial ovarian cancer.Methods In order to reveal the mechanism of chemokines mediating epithelial ovarian cancer abdominal cavity metastasis,the expressions of chemokine receptor and its ligand in the epithelial ovarian carcinoma tissue and the peritoneal tissue were detected by RT-PCR and immunohistochemical.Results The expression of chemokine receptor CXCR4 in the epithelial ovarian carcinoma tissue was significantly higher than that of other chemokine receptors (P <0.01).The CXCR4 ligand SDF-1 was high-expressed in the epithelial ovarian carcinoma tissue and the peritoneal tissue.Conclusion The CXCR4 and SDF-1 are high-ex-pressed in the ovarian cancer tissue and may stimulate the excessive growth of ovarian cancer cells by the autocrine function;SDF-1 in the peritoneal tissue is high-expressed and may mediate the ovarian cancer cells expressing CXCR4 transferred to the abdominal cavity.

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