| Literature DB >> 28754672 |
Wei Du1, Xing Xu1, Qing Niu1, Xuexi Zhang1, Yiliang Wei1, Ziqiao Wang1,2, Wei Zhang1, Jun Yan3, Yongxin Ru4, Zheng Fu1,5, Xiaobo Li1, Yuan Jiang1,5, Zhenyi Ma1,5, Zhenfa Zhang6, Zhi Yao1,5, Zhe Liu7,5.
Abstract
Dissociation from epithelial sheets and invasion through the surrounding stroma are critical early events during epithelial cancer metastasis. Here we find that a lymphocyte lineage-restricted transcription factor, Spi-B, is frequently expressed in human lung cancer tissues. The Spi-B-expressing cancer cells coexpressed vimentin but repressed E-cadherin and exhibited invasive behavior. Increased Spi-B expression was associated with tumor grade, lymphatic metastasis, and short overall survival. Mechanistically, Spi-B disrupted intercellular junctions and enhanced invasiveness by reconfiguring the chromatin structure of the tight junction gene claudin-2 (CLDN2) and repressing its transcription. These data suggest that Spi-B participates in mesenchymal invasion, linking epithelial cancer metastasis with a lymphatic transcriptional program. Cancer Res; 77(18); 4809-22. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 28754672 DOI: 10.1158/0008-5472.CAN-17-0020
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701