| Literature DB >> 27443606 |
Jianlu Kong1, Wenjie Sun1, Chen Li1, Ledong Wan1, Shuo Wang1, Yihua Wu1, Enping Xu1, Honghe Zhang2, Maode Lai3.
Abstract
Long non-coding RNAs (lncRNAs) play crucial roles in many biological and pathological processes, including tumor metastasis. Here we reported a novel lncRNA, LINC01133 that was downregulated by TGF-β, which could inhibit epithelial-mesenchymal transition (EMT) and metastasis in colorectal cancer (CRC) cells. An alternative splicing factor SRSF6 was identified to directly interact with LINC01133, and SRSF6 promoted EMT and metastasis in CRC cells independent of LINC01133 And we confirmed that the EMT process was regulated by LINC01133 in CRC cells dependent on the presence of SRSF6. The observation for LINC01133 to inhibit metastasis was also verified in vivo. Moreover clinical data showed that the LINC01133 expression was positively correlated with E-cadherin, and negatively correlated with Vimentin, and there was a robust association of low LIINC01133 expression in tumors with poor survival in CRC samples. These data suggest that LINC01133 inhibits the EMT and metastasis by directly binding to SRSF6 as a target mimic, and may serve as a prognostic biomarker and an effective target for anti-metastasis therapies for CRC.Entities:
Keywords: Colorectal cancer; EMT; Metastasis; SRSF6; lncRNA
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Year: 2016 PMID: 27443606 DOI: 10.1016/j.canlet.2016.07.015
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679