Gankyrin Promotes Tumor Growth and Metastasis Through Activation of IL-6/STAT3 Signaling in Human Cholangiocarcinoma

被引:143
作者
Zheng, Tongsen [1 ]
Hong, Xuehui [1 ]
Wang, Jiabei [1 ]
Pei, Tiemin [1 ]
Liang, Yingjian [1 ]
Yin, Dalong [1 ]
Song, Ruipeng [1 ]
Song, Xuan [1 ]
Lu, Zhaoyang [1 ]
Qi, Shuyi [2 ]
Liu, Jiaren [3 ,4 ]
Sun, Boshi [1 ]
Xie, Changming [1 ]
Pan, Shangha [1 ]
Li, Yuejin [1 ]
Luo, Xiaohe [1 ]
Li, Shuai [1 ]
Fang, Xiang [5 ]
Bhatta, Nishant [1 ]
Jiang, Hongchi [1 ]
Liu, Lianxin [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Key Lab Hepatosplen Surg, Minist Educ,Dept Gen Surg, Harbin 150001, Heilongjiang Pr, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 1, Dept Gerontol, Harbin 150001, Heilongjiang Pr, Peoples R China
[3] Childrens Hosp, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Harbin Med Univ, Affiliated Hosp 1, Dept Pathol, Harbin 150001, Heilongjiang Pr, Peoples R China
关键词
CELL-CYCLE; S6; ATPASE; OVEREXPRESSION; ONCOPROTEIN; EXPRESSION; PROTEIN; P53; HEPATOCYTES; ASSOCIATION; DEGRADATION;
D O I
10.1002/hep.26705
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Although gankyrin is involved in the tumorigenicity and metastasis of some malignancies, the role of gankyrin in cholangiocarcinoma (CCA) is unclear. In this study we investigated the expression of gankyrin in human CCA tissues and cell lines. The effects of gankyrin on CCA tumor growth and metastasis were determined both in vivo and in vitro. The results showed that gankyrin was overexpressed in CCA tissues and cell lines. Gankyrin expression was associated with CCA histological differentiation, TNM stage, and metastasis. The multivariate Cox analysis revealed that gankyrin was an independent prognostic indicator for overall survival. Gankyrin overexpression promoted CCA cell proliferation, migration, and invasion, while gankyrin knockdown inhibited CCA tumor growth, metastasis, and induced Rb-dependent senescence and G(1) phase cell cycle arrest. Gankyrin increased the phosphorylation of signal transducer and activator of transcription 3 (STAT3) and promoted the nuclear translocation of p-STAT3. Suppression of STAT3 signaling by small interfering RNA (siRNA) or STAT3 inhibitor interfered with gankyrin-mediated carcinogenesis and metastasis, while interleukin (IL)-6, a known upstream activator of STAT3, could restore the proliferation and migration of gankyrin-silenced CCA cells. The IL-6 level was decreased by gankyrin knockdown, while increased by gankyrin overexpression. Gankyrin regulated IL-6 expression by way of facilitating the phosphorylation of Rb; meanwhile, rIL-6 treatment increased the expression of gankyrin, suggesting that IL-6 was regulated by a positive feedback loop involving gankyrin in CCA. In the xenograft experiments, gankyrin overexpression accelerated tumor formation and increased tumor weight, whereas gankyrin knockdown showed the opposite effects. The in vivo spontaneous metastasis assay revealed that gankyrin promoted CCA metastasis through IL-6/STAT3 signaling pathway. Conclusion: Gankyrin is crucial for CCA carcinogenesis and metastasis by activating IL-6/STAT3 signaling pathway through down-regulating Rb protein. (Hepatology 2014;59:935-946)
引用
收藏
页码:935 / 946
页数:12
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