Kindlin-2 promotes clear cell renal cell carcinoma progression through the Wnt signaling pathway

被引:8
|
作者
Li, Muhan [1 ,2 ,3 ,4 ]
Pei, Xuelian [1 ,2 ,5 ,6 ,7 ]
Wang, Guoliang [8 ]
Zhan, Jun [1 ,2 ,5 ]
Du, Juan [1 ,2 ,5 ]
Jiang, Hao [1 ,2 ,5 ]
Tang, Yan [1 ,2 ,5 ]
Zhang, Hongquan [1 ,2 ,5 ]
He, Huiying [1 ,2 ,3 ,4 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Minist Educ, Key Lab Carcinogenesis & Translat Res, Beijing 100191, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[3] Peking Univ, Hlth Sci Ctr, Dept Pathol, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[4] Peking Univ, Hosp 3, Beijing 100191, Peoples R China
[5] Peking Univ, Hlth Sci Ctr, Dept Anat Histol & Embryol, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[6] Shihezi Univ, Sch Med, Dept Histol & Embryol, Shihezi 832000, Xinjiang, Peoples R China
[7] Shihezi Univ, Sch Med, Key Lab Xinjiang Endem & Ethn Dis, Minist Educ, Shihezi 832000, Xinjiang, Peoples R China
[8] Peking Univ, Hosp 3, Dept Urol, Beijing 100083, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Kindlin-2; CCRCC; prognosis; migration; invasion; Wnt pathway; GASTRIC-CANCER CELLS; BETA-CATENIN; ADHESION; INVASION; METASTASIS; EXPRESSION; COMPLEX; BINDING;
D O I
10.3892/or.2017.5789
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Kindlin-2 is an integrin-interacting, FERM-domain containing protein, which plays a critical role in tumor progression. However, the specific role of Kindlin-2 in renal cell carcinoma (RCC) progression has not been described. In this study we investigated the role of Kindlin-2 in progression of clear cell RCC (CCRCC), which is the most common RCC subtype, and its underlying mechanisms. Immunohistochemistry studies show that expression of Kindlin-2 in CCRCC is positively correlated with tumor grade, and Kindlin-2 expression in advanced CCRCC with lymph node metastasis was greater than in localized CCRCC. Kindlin-2 expression in CCRCC tumor specimens is also correlated with short patient survival, but is not an independent prognostic factor. Kindlin-2 promotes CCRCC cell migration and invasion in vitro, whereas knockdown of Kindlin-2 inhibited cell migration and invasion. Knockdown of Kindlin-2 also inhibits ACHN cell proliferation in vitro and tumorigenesis in vivo. Kindlin-2 may be required for Wnt pathway activation which underlies the mechanisms of Kindlin-2 promoting CCRCC progression. These findings demonstrate that expression of Kindlin-2 is associated with tumor grade, lymph node metastasis and poor prognosis in CCRCC patients. Kindlin-2 may regulate CCRCC progression through the Wnt signaling pathway, promoting CCRCC cell proliferation, migration and invasion.
引用
收藏
页码:1551 / 1560
页数:10
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