| Literature DB >> 26948025 |
Cai-Yong Lai1,2, Yin Xu1, Gan-Shen Yu1, Xun Wu1, Yun-Fei Li1, Bin Pan1, Bao-Li Heng1, Yi-Jun Xue2, Ze-Xuan Su3.
Abstract
Our preliminary study indicated that Engrailed-2 (EN2) is downregulated but also ectopically expressed in clear-cell renal cell carcinoma (CCRCC), and the absence of EN2 expression was associated with poor histological grade. However, the specific roles of EN2 in CCRCC have yet to be elucidated. In the present study, we examined the effects of inhibiting EN2 expression by human renal tubular epithelial cells (HK-2) and overexpressing EN2 by human clear-cell renal cells (786-O). Results showed that EN2 inhibition accelerated HK-2 cell proliferation, shortened the cell cycle, reduced apoptosis, and acted more invasively. By contrast, EN2 overexpression in 786-O cells decelerated the proliferative ability of 786-O, increased the percentage of cell apoptosis, and weakened the invasive ability. Overall, the results demonstrated that EN2 might play an anti-oncogenic role in oncogenesis and development of CCRCC, thereby maintaining the normal growth of human renal tubular epithelial cells.Entities:
Keywords: Anti-oncogene; Clear-cell renal cell carcinoma; Engrailed-2
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Year: 2016 PMID: 26948025 DOI: 10.1007/s10735-016-9665-4
Source DB: PubMed Journal: J Mol Histol ISSN: 1567-2379 Impact factor: 2.611