| Literature DB >> 30502359 |
Min Xie1, Tianshi Ma2, Jiangyang Xue3, Hongwei Ma4, Ming Sun5, Zhihong Zhang6, Minjuan Liu7, Yinghua Liu8, Songwen Ju9, Zhaoxia Wang10, Wei De11.
Abstract
Multiple studies have revealed that long non-coding RNAs (lncRNAs) extensively participate in human cancer malignant progression. The long intergenic non-protein coding RNA 707 (LINC00707), 3087 bp in length, was recently reported to be an essential oncogene in promoting lung adenocarcinoma cell proliferation and metastasis. However, its role in gastric cancer (GC) remains unclear. In this study, we identified that LINC00707 was excessively expressed in GC tissues and correlated with advanced stage, larger tumor size, lymph node metastasis and poorer prognosis in GC patients. In vitro and in vivo assays showed that LINC00707 promote GC cell proliferation and metastasis. Mechanistically, LINC00707 could abundantly interact with mRNA stabilizing protein HuR; "LINC00707-HuR" coalition ulteriorly combined with VAV3/F11R mRNAs and increased their stability. Taken together, our findings prove that LINC00707 may act as an oncogene in GC by regulating mRNA stability and serve as a potential target for GC diagnosis and prognosis.Entities:
Keywords: F11R; VAV3; lncRNA; “LINC00707-HuR” coalition
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Year: 2018 PMID: 30502359 DOI: 10.1016/j.canlet.2018.11.032
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679