Deleted in liver cancer-1 inhibits cell growth and tumorigenicity in human pancreatic cancer

被引:6
|
作者
Zheng, Zhenjiang [1 ]
Tan, Chunlu [2 ]
Xiang, Guangming [2 ]
Mai, Gang [2 ]
Liu, Xubao [2 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp Chengdu 2, Peoples Hosp Chengdu 3, Dept Gen Surg, Chengdu 610031, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Hepatobiliopancreat Surg, Chengdu 610041, Sichuan, Peoples R China
关键词
deleted in liver cancer; tumor suppressor gene; gene therapy; pancreatic cancer; GTPASE-ACTIVATING PROTEIN; TUMOR-SUPPRESSOR GENE; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; DLC-1; GENE; FOCAL ADHESIONS; RHOGAP PROTEIN; IN-VIVO; EXPRESSION; PROLIFERATION;
D O I
10.3892/ol.2013.1415
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Deleted in liver cancer-1 (DLC-1) has been isolated from primary hepatocellular carcinoma and demonstrated to be a potential tumor suppressor gene. The aim of the present study was to observe the effect of the DLC-1 gene on pancreatic cancer cell growth and evaluate the feasibility of using the DLC-1 gene in gene therapy for pancreatic cancer. A recombinant plasmid (pcDNA3.1/DLC-1) was transfected into PANC-1 cells by liposomes and then the pre-established human PANC-1 pancreatic carcinoma cells were injected into athymic nude mice via the tail vein. The results showed that the overexpression of DLC-1 in the PANC-1 cells inhibited cell proliferation in vitro, while the act of introducing DLC-1 reduced tumorigenicity in the nude mice. The findings suggest that DLC-1 may have an effect on the pathogenesis of pancreatic cancer. The DLC-1 gene may be a promising target in gene therapy for pancreatic cancer.
引用
收藏
页码:521 / 524
页数:4
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