| Literature DB >> 28605165 |
Hui Chen1, Xiao Gao1, Zhengwang Sun2, Qingwei Wang1, Di Zuo3, Linian Pan1, Kun Li1, Jiwei Chen2, Geng Chen1, Kewen Hu1, Ke Li1, Abdus Saboor Shah1, Tingmei Huang1, Bhatti Muhammad Zeeshan1, Lu Tong1, Chan Jiao1, Jian Liu4, Tenghui Chen5, Liangfang Yao1, Yongyan Dang1, Tielong Liu2, Lei Li1.
Abstract
It has been reported that the proteasome activator REGγ is associated with multiple oncogenic pathways in human cancers. However, the role of REGγ in the development of melanoma and the underlying mechanisms remain unclear. In this study, we attempted to investigate the effects of REGγ on human melanoma cell proliferation in vitro and in vivo. We demonstrated that knockdown of REGγ inhibited melanoma cell growth and arrested melanoma cell at G1 phase. Furthermore, depletion of REGγ also inhibited the xenograft growth of human melanoma. Mechanistically, REGγ activates Wnt/β-catenin signal pathway by degrading GSK-3β in melanoma cell lines and mouse models. Transient knockdown of β-catenin effectively blocked cell proliferation in REGγ wild-type melanoma cells. In human melanoma samples, REGγ was overexpressed and positively correlated with β-catenin levels. This study demonstrates that REGγ is a central molecule in the development of melanoma by regulating Wnt/β-catenin pathway. This suggests that targeting REGγ could be an alternative therapeutic approach for melanoma.Entities:
Keywords: GSK-3β; REGγ; Wnt/β-catenin; melanoma
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Year: 2017 PMID: 28605165 DOI: 10.1111/exd.13394
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960