Abstract | UNLABELLED: MATERIALS AND METHODS: Using the technique of RNA interference, the expression of CLIC1 was downregulated in the PC-3 and DU145 cell lines. MTT assay, Transwell chamber, and flow cytometry were used to determine the effect of CLIC1 on the proliferation, migration, and apoptosis ability of PC-3 and DU145 cells. The levels of phosphorylated extracellular signal-regulated kinase 1/2 (p-ERK1/2), ERK1/2, matrix metalloproteinase (MMP)-2, and MMP-9 were examined by western blotting. RESULTS: The results showed that the knockdown of CLIC1 exerts inhibitory effects on the proliferation and migration of PC-3 and DU145 cells. At the same time, the authors found that the knockdown of CLIC1 has no effect on the apoptosis in PC-3 and DU145 cells. Meanwhile, the levels of p-ERK1/2, MMP-2, and MMP-9 were decreased in the CLIC1 small interfering RNA ( siRNA) group compared with the control and vector groups. CONCLUSION:
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Authors | Yudong Tian, Yanbin Guan, Yongyan Jia, Qingjun Meng, Jinjian Yang |
Journal | Cancer biotherapy & radiopharmaceuticals
(Cancer Biother Radiopharm)
Vol. 29
Issue 8
Pg. 339-44
(Oct 2014)
ISSN: 1557-8852 [Electronic] United States |
PMID | 25279971
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- CLIC1 protein, human
- Chloride Channels
- Mitogen-Activated Protein Kinase 1
- Mitogen-Activated Protein Kinase 3
- MMP2 protein, human
- Matrix Metalloproteinase 2
- MMP9 protein, human
- Matrix Metalloproteinase 9
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Topics |
- Apoptosis
(physiology)
- Cell Growth Processes
(physiology)
- Cell Line, Tumor
- Cell Movement
(physiology)
- Chloride Channels
(genetics, metabolism)
- Humans
- MAP Kinase Signaling System
(physiology)
- Male
- Matrix Metalloproteinase 2
(metabolism)
- Matrix Metalloproteinase 9
(metabolism)
- Mitogen-Activated Protein Kinase 1
(metabolism)
- Mitogen-Activated Protein Kinase 3
(metabolism)
- Prostatic Neoplasms
(enzymology, genetics, metabolism, pathology)
- RNA Interference
- Transfection
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