LASP-1 induces proliferation, metastasis and cell cycle arrest at the G2/M phase in gallbladder cancer by down-regulating S100P via the Pl3K/AKT pathway

被引:43
作者
Li, ZhiZhen [1 ,2 ,3 ]
Chen, YuanYuan [1 ,2 ,3 ]
Wang, XuAn [1 ,2 ,3 ]
Zhang, HongChen [1 ,2 ,3 ]
Zhang, Yijian [1 ,2 ,3 ]
Gao, YaoHui [1 ,2 ,3 ]
Weng, Mingzhe [1 ,2 ,3 ]
Wang, Lei [1 ,2 ,3 ]
Liang, HaiBin [1 ,2 ,3 ]
Li, MaoLan [1 ,2 ,3 ]
Zhang, Fei [1 ,2 ,3 ]
Zhao, Shuai [1 ,2 ,3 ]
Liu, Shibo [1 ,2 ,3 ]
Cao, Yang [1 ,2 ,3 ]
Shu, Yijun [1 ,2 ,3 ]
Bao, Runfa [1 ,2 ,3 ]
Zhou, Jian [1 ,2 ,3 ]
Liu, Xiyong [1 ,2 ,3 ]
Yan, Yun [1 ,2 ,3 ]
Zhen, Lei [1 ,2 ,3 ]
Dong, Qian [1 ,2 ,3 ]
Liu, Yingbin [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Gen Surg, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Lab Gen Surg, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Inst Biliary Tract Dis Res, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
Gallbladder cancer; LASP-1; S100P; Proliferation; Metastasis; Cell cycle; SH3; PROTEIN-1; HEPATOCELLULAR-CARCINOMA; PANCREATIC-CANCER; BREAST-CANCER; SNP DISCOVERY; MIGRATION; SURVIVAL; LIM; OVEREXPRESSION; LOCALIZATION;
D O I
10.1016/j.canlet.2016.01.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
LASP-1 is an actin-binding protein that regulates cytoskeletal dynamics and cell migration. LASP-1 was previously identified in a cDNA library from metastatic breast cancer samples. This protein has since been detected in multiple human cancers, including liver cancer, gastric cancer and pancreatic cancer. S100P is a small calcium-binding protein in the 5100 protein family that regulates cellular, physiological and pathological processes in various cancers. However, the clinical significance of LASP-1 and S100P expression in gallbladder cancer (GBC) is not yet clear. In our study, we focused on the clinical significance, biological function and mechanism of LASP-1 in gallbladder cancer and detected LASP-1 and S100P overexpression in GBC tissues. The expression of LASP-1 was significantly correlated with poor prognosis in GBC patients (P < 0.05). Furthermore, down-regulation of LASP-1 expression resulted in the obvious inhibition of proliferation and migration and caused cell cycle arrest by down-regulating S100P via the PI3K/AKT pathway; in mice, tumor volume was signifidantly decreased. In conclusion, LASP-1 may act as an oncogene to regulate the expression of S100P to influence cellular functions in GBC. LASP-1 could serve as a genetic treatment target in GBC patients. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:239 / 250
页数:12
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