4.7 Article

Reduced LINC00551 expression promotes proliferation and invasion of esophageal squamous cancer by increase in HSP27 phosphorylation

期刊

JOURNAL OF CELLULAR PHYSIOLOGY
卷 236, 期 2, 页码 1418-1431

出版社

WILEY
DOI: 10.1002/jcp.29947

关键词

esophageal squamous cell carcinoma; HSP27; invasion; lncRNA LINC00551; proliferation

资金

  1. National Natural Science Foundation of China [81672308, 81673516]
  2. Hunan Provincial Science and Technology Department [2017JJ2345]
  3. Hunan Provincial Key Area RD Programmes [2019SK2253]

向作者/读者索取更多资源

The lncRNA LINC00551 plays a significant role in ESCC development and progression, with downregulated expression associated with poor prognosis for ESCC patients. Overexpression of LINC00551 inhibits ESCC cell proliferation and invasion, while knockdown promotes these processes. LINC00551 binds to HSP27 and decreases its phosphorylation, thereby regulating ESCC cell proliferation and invasion.
Esophageal squamous cell carcinoma (ESCC) is one of the deadliest cancers, and long noncoding RNAs (lncRNAs) regulate gene expression or activities. This study investigated the role of lncRNA LINC00551 in ESCC development and progression. Three paired ESCC and normal tissues were subjected to next-generation sequencing and we identified 82 upregulated and 60 downregulated lncRNAs, including LINC00551, which was confirmed to markedly downregulated in 78 ESCC tissues and in the Gene Expression Profiling Interactive Analysis data set. Downregulated LINC00551 expression was associated with lymph node metastasis, advanced TNM stage, and tumor size. Moreover, downregulated LINC00551 expression was also associated with poor progression-free survival and overall survival of ESCC patients. In vitro and in vivo, LINC00551 overexpression inhibited ESCC cell proliferation and invasion, whereas knockdown of LINC00551 expression promoted ESCC cell proliferation and invasion. RNA pull-down and mass spectrometry assays identified the potential LINC00551 binding proteins, and HSP27 was a promising LINC00551 targeting proteins after RNA immunoprecipitation assay. At the protein level, LINC00551 bound to and decreased HSP27 phosphorylation, and in turn, downregulated ESCC cell proliferation and invasion. The current study demonstrated the functional significance of LINC00551 in ESCC development, progression, and prognosis. Further study will assess LINC00551 as a novel prognostic marker or therapeutic target for ESCC.

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