Gankyrin promotes tumor growth and metastasis through activation of IL-6/STAT3 signaling in human cholangiocarcinoma

车站3 癌症研究 转移 信号转导 医学 生物 癌症 细胞生物学 内科学
作者
Tongsen Zheng,Xuehui Hong,Jiabei Wang,Tiemin Pei,Yingjian Liang,Dalong Yin,Ruipeng Song,Xuan Song,Zhao‐Yang Lu,Shuyi Qi,Jia Liu,Boshi Sun,Changming Xie,Shangha Pan,Yuejin Li,Xiaohe Luo,Shuai Li,Xiang Fang,Nishant Bhatta,Hongchi Jiang
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:59 (3): 935-946 被引量:99
标识
DOI:10.1002/hep.26705
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)
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
紫枫完成签到,获得积分10
2秒前
JUN完成签到,获得积分10
3秒前
ll完成签到,获得积分10
5秒前
瞿人雄完成签到,获得积分10
6秒前
没心没肺完成签到,获得积分10
8秒前
时代更迭完成签到 ,获得积分10
10秒前
12秒前
学术霸王完成签到,获得积分10
13秒前
隐形曼青应助科研通管家采纳,获得10
14秒前
Jerry完成签到,获得积分10
14秒前
叨叨发布了新的文献求助10
15秒前
22秒前
刘可完成签到 ,获得积分10
23秒前
谢大喵发布了新的文献求助10
24秒前
zhangguo完成签到 ,获得积分10
26秒前
叨叨完成签到,获得积分10
28秒前
夜霄咕咕鸽完成签到 ,获得积分10
28秒前
孙晓燕完成签到 ,获得积分10
28秒前
1111111111发布了新的文献求助30
28秒前
sandyleung完成签到 ,获得积分10
30秒前
青水完成签到 ,获得积分10
33秒前
wushuimei完成签到 ,获得积分0
34秒前
Young完成签到 ,获得积分10
35秒前
snubdisphenoid完成签到 ,获得积分10
36秒前
谦让又琴发布了新的文献求助10
36秒前
昵称什么的不重要啦完成签到 ,获得积分10
37秒前
阿童木完成签到 ,获得积分10
37秒前
38秒前
wdmz发布了新的文献求助10
44秒前
九花青完成签到,获得积分10
46秒前
爆米花应助Liangstar采纳,获得10
48秒前
娅娃儿完成签到 ,获得积分10
56秒前
AmyHu完成签到,获得积分10
58秒前
111完成签到 ,获得积分10
58秒前
AbdoSpace完成签到,获得积分10
1分钟前
yushiolo完成签到 ,获得积分10
1分钟前
cqnuly完成签到,获得积分10
1分钟前
1分钟前
长情的八宝粥完成签到 ,获得积分10
1分钟前
不是吧不是吧完成签到 ,获得积分10
1分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Lewis’s Child and Adolescent Psychiatry: A Comprehensive Textbook Sixth Edition 2000
Cronologia da história de Macau 1600
Treatment response-adapted risk index model for survival prediction and adjuvant chemotherapy selection in nonmetastatic nasopharyngeal carcinoma 1000
Lloyd's Register of Shipping's Approach to the Control of Incidents of Brittle Fracture in Ship Structures 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
Atlas of Anatomy 5th original digital 2025的PDF高清电子版(非压缩版,大小约400-600兆,能更大就更好了) 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6203184
求助须知:如何正确求助?哪些是违规求助? 8030030
关于积分的说明 16720002
捐赠科研通 5295147
什么是DOI,文献DOI怎么找? 2821547
邀请新用户注册赠送积分活动 1801044
关于科研通互助平台的介绍 1662993