肾透明细胞癌
基因沉默
癌症研究
转移
E2F1
细胞生长
医学
癌症
转录因子
肾细胞癌
生物
病理
细胞周期
内科学
生物化学
遗传学
基因
作者
Yu Gao,Hongzhao Li,Xin Ma,Fan Yang,Dong Ni,Yu Zhang,Qingbo Huang,Kan Liu,Xintao Li,Lei Wang,Liangyou Gu,Yuanxin Yao,Qing Ai,Qingshan Du,Erlin Song,Xu Zhang
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2016-10-26
卷期号:77 (2): 330-342
被引量:70
标识
DOI:10.1158/0008-5472.can-16-0348
摘要
The transcription factor KLF6 has an essential role in the development and metastasis of multiple human cancers. Paradoxically, KLF6 expression was found to be attenuated in primary metastatic clear cell renal cell carcinoma (ccRCC), such that it is unclear how KLF6 affects malignant progression in this setting. In this study, we demonstrate that KLF6 attenuation in renal cells is sufficient to promote E2F1-mediated epithelial-mesenchymal transition and metastatic prowess. In a mouse xenograft model of human ccRCC, silencing KLF6 increased tumor cell proliferation and malignant character, whereas E2F1 silencing reversed these properties. These effects were corroborated in a metastatic model system, where we observed a greater number of pulmonary metastatic lesions formed by ccRCC cells where KLF6 was silenced and E2F1 enforced. Analysis of clinical specimens of ccRCC revealed that low levels of KLF6 and high levels of E2F1 correlated closely with ccRCC development. Overall, our results established the significance of activating the KLF6-E2F1 axis in aggressive ccRCC, defining a novel critical signaling mechanism that drives human ccRCC invasion and metastasis. Cancer Res; 77(2); 330-42. ©2016 AACR.
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