Abstract | OBJECTIVE: METHODS: The PCDGF- shRNA expression vector was transfected into the Eca-109 cells by liposome. After transfection, the mRNA and protein expressions of PCDGF were detected by RT-PCR and Western-blot respectively. Cell Counting Kit-8 (CCK-8) assay and Boyden chamber method were performed to measure the cell proliferation and invasion ability respectively. RESULTS: The expression levels of PCDGF mRNA and protein were both decreased in Eca-109 cells transfected with PCDGF- shRNA expression vector (transfection group). Twenty-four, 48 and 72 h after transfection, the cells proliferation in the transfection group was inhibited, and the inhibition rate was 20.4%, 21.1% and 20.9% respectively. The cell proliferation activity in the transfection group was significantly lower than that in the non-transfection group, liposome group and negative vector group (all P<0.05). The number of cell migration in the non-transfection group,negative vector group, liposome group and transfection group was 118.8±12.0, 100.8±9.0, 114.3±4.7, and 53.5±16.3 respectively. The differences were statistically significant between the transfection group and the other 3 groups (all P<0.05). CONCLUSIONS: PCDGF RNA interference can inhibit the proliferation and invasion abilities of esophageal squamous carcinoma cells in vitro. PCDGF gene may be the new target of gene therapy.
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Authors | Qing-feng Zheng, Shuo-yan Liu, Hai-yan Wang, Feng Wang, Zhen Wang, Xiao-feng Chen, Jian-jian Wang, Min-gang Ying, Xiong-wei Zheng, Xian-dong Lin, Zhi-feng Zhou, Fu-sheng Gong, Yun-qing Xie |
Journal | Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery
(Zhonghua Wei Chang Wai Ke Za Zhi)
Vol. 16
Issue 9
Pg. 874-7
(Sep 2013)
ISSN: 1671-0274 [Print] China |
PMID | 24061998
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- GRN protein, human
- Intercellular Signaling Peptides and Proteins
- Progranulins
- RNA, Small Interfering
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Topics |
- Carcinoma, Squamous Cell
(metabolism, pathology)
- Cell Line, Tumor
- Cell Proliferation
- Esophageal Neoplasms
(metabolism, pathology)
- Esophageal Squamous Cell Carcinoma
- Genetic Vectors
- Humans
- Intercellular Signaling Peptides and Proteins
(genetics, metabolism)
- Progranulins
- RNA Interference
- RNA, Small Interfering
(genetics)
- Transfection
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