Expression of LAPTM4B in Gallbladder Carcinoma Cells: The Role in Invasive Potential

被引:0
|
作者
Zhou, Li [1 ]
He, Xiao-Dong [1 ]
Yu, Jian-Chun [1 ]
Zhou, Rou-Li [2 ]
Xiong, Fu-Xia [2 ]
Qu, Qiang [1 ]
Rui, Jing-An [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Peking Union Med Coll, Dept Gen Surg, Beijing 100730, Peoples R China
[2] Peking Univ, Sch Basic Med Sci, Dept Cell Biol, Beijing 100191, Peoples R China
关键词
LAPTM4B; Expression; Migration; Invasion; GBC-SD; HEPATOCYTE GROWTH-FACTOR; HEPATOCELLULAR-CARCINOMA; GENE-EXPRESSION; IN-VITRO; CANCER; SURVIVAL; OVEREXPRESSION; CARCINOGENESIS; PROGRESSION; INHIBITION;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: It was previously established that LAPTM4B-35 highly expressed in gallbladder carcinoma and being of clinicopathological and prognostic significances. However, expression of LAPTM4B gene in gallbladder carcinoma (GBC-SD), a gallbladder carcinoma cell line, and its role in invasive potential remain unclear. Methodology: Expression of LAPTM4B in GBC-SD cells was first detected. Plasmids, pcDNA3-AE (containing complete open reading frame of LAPTM4B) and Mock (pcDNA3), were transiently transfected into GBC-SD cells. Invasive phenotypes (migration and invasion) and relative molecules were then shown by transwell assay, crossing river test and Western blot analysis. Results: Immunocytochemical staining revealed that LAPTM4B-35 positively expressed in cytoplasm of GBC-SD cells. But LAPTM4B-35 expression was obviously weaker in GBC-SD cells than that in BEL-7402 cells (positive control). Besides, cells transfected with pcDNA3-AE presented shorter crossing river time, less migrated and invaded cell numbers, compared with cells transfected with the Mock plasmid and parent cells. Finally, increased expressions of active uPA, MMP-9, pro MMP-2 and active MMP-2 were also observed in cells transfected with pcDNA3-AE. Conclusions: Our data suggested that LAPTM4B expressed in GBC-SD cells at a relatively low level. Forced overexpression of LAPTM4B increased invasive potential of GBC-SD cells, through modulating molecules associated with degradation of extracellular matrix.
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页码:207 / 211
页数:5
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