The role of galectin-3 in the tumorigenesis and progression of pituitary tumors

被引:14
|
作者
Diao, Bo [1 ,2 ]
Liu, Ying [3 ]
Xu, Guo-Zheng [1 ,2 ]
Zhang, Yi [4 ]
Xie, Jun [5 ]
Gong, Jie [1 ,2 ]
机构
[1] Wuhan Gen Hosp Guangzhou Command, Dept Neurosurg, 627 Wuluo Rd, Wuhan 430070, Hubei, Peoples R China
[2] Hubei Key Lab Cent Nervous Syst Tumor & Intervent, 627 Wuluo Rd, Wuhan 430070, Hubei, Peoples R China
[3] Wuhan Gen Hosp Guangzhou Command, Dept Clin Lab, Wuhan 430070, Hubei, Peoples R China
[4] Wuhan Gen Hosp Guangzhou Command, Dept Clin Expt, Wuhan 430070, Hubei, Peoples R China
[5] Wuhan Gen Hosp Guangzhou Command, Dept Sci & Training, 627 Wuluo Rd, Wuhan 430070, Hubei, Peoples R China
关键词
pituitary adenomas; galectin-3; proliferation; apoptosis; migration; GENE-EXPRESSION; CANCER;
D O I
10.3892/ol.2018.7931
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Galectin-3 (Gal-3), a beta-galactoside-binding protein, has been implicated in cell proliferation, cell adhesion, and the progression and metastasis of various types of cancer. The present study investigated the involvement of Gal-3 in the tumorigenesis and progression of pituitary tumors using three rat pituitary tumor cell lines. Following transfection with Gal-3 expression and interference vectors, the impact of Gal-3 on proliferation, apoptosis and migration of pituitary tumor cells was been investigated. Meanwhile, BCL2 associated X, apoptosis regulator (Bax), caspase-3 and matrix metalloproteinase 7 (MMP7) protein expression levels were analyzed by western blotting. The results of the present study revealed that Gal-3 expression in GH3 and GH4C1 cells was higher than in RC-4B/C cells. Furthermore, Gal-3 was demonstrated to promote the proliferation and migration of GH3 and GH4C1 cells, and inhibit cell apoptosis. Caspase-3 and MMP7 protein expression was also increased by Gal-3, while Bax expression was decreased. These results suggested that Gal-3 serves an important function in the tumorigenesis and development of pituitary tumors, and it may be a useful target for the treatment of pituitary tumors in the future.
引用
收藏
页码:4919 / 4925
页数:7
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