Title of article
BZW1, a novel proliferation regulator that promotes growth of salivary muocepodermoid carcinoma
Author/Authors
Li، نويسنده , , Shaoqing and Chai، نويسنده , , Zhiguo and Li، نويسنده , , Yan and Liu، نويسنده , , Daqing and Bai، نويسنده , , Zhongcheng and Li، نويسنده , , Yan and Li، نويسنده , , Yunming and Situ، نويسنده , , Zhenqiang، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
9
From page
86
To page
94
Abstract
Mucoepidermoid carcinoma (MEC) is the most common primary malignancy in the salivary glands; however, its oncogenesis is poorly understood. Here, we show that the homo sapiens basic leucine zipper and W2 domains 1 (BZW1 or BZAP45) is a critical factor in the regulation of MEC growth. Firstly, BZW1 was highly expressed in MEC tissues and cells, determined by quantitative real time polymerase chain reaction. Higher levels of BZW1 proteins were detected in MEC tissues, particularly in high-grade MEC, by immunohistochemistry. Furthermore, down-regulation of BZW1 expression by infection with BZW1-specific RNAi-expressing lentivirus inhibited Mc3 cell proliferation and colony formation in vitro. In addition, down-regulation of BZW1 expression arrested Mc3 cell cycling at the G0/G1 phase and mitigated Mc3 cell migration and invasiveness in vitro, determined by wound healing and transwell invasion assays. Importantly, down-regulation of BZW1 expression significantly reduced the tumorigenicity of Mc3 cells in vivo, evidenced by the slow progression of small tumors induced by BZW1-specific RNAi expressing Mc3 cells. Apparently, BZW1 is a novel factor, promoting the growth of MEC cells. Our findings may provide a base for design of new strategy for diagnosis and therapy for human MEC.
Keywords
mucoepidermoid carcinoma , BZW1 , Cell cycling , Tumorigenicity
Journal title
Cancer Letters
Serial Year
2009
Journal title
Cancer Letters
Record number
1817793
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