4.2 Article

Long Noncoding RNA Linc00152 Functions as a Tumor Propellant in Pan-Cancer

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 44, 期 6, 页码 2476-2490

出版社

KARGER
DOI: 10.1159/000486170

关键词

Linc00152; Tumorigenesis; Pan-cancer; Breast cancer

资金

  1. Heilong Jiang province Health and Family Planning Commission Foundation Grant [2016-087]
  2. National Natural Science Foundation of China [81602323]
  3. China Postdoctoral Science Foundation Grant [2016M600262]
  4. Heilong Jiang postdoctoral Foundation Grant [LBH-Z16163]
  5. Wu Lien-teh Science Foundation of Harbin Medical University [WLD-QN1706]
  6. Young Elite Training Foundation Grant of Harbin Medical University Cancer Hospital [JY2016-02]

向作者/读者索取更多资源

Background/Aims: The oncogenic role of linc00152 in pan-cancer is unclear. Methods: In this study, RNA-Seq of 33 breast specimens was performed, and the expression of linc00152 was validated by qPCR using 50 paired breast cancer tissues and adjacent normal tissues. This result combined with the expression of linc00152 in pan-cancer was revalidated by Gene Expression Omnibus and The Cancer Genome Atlas data. Next, the oncogenic roles of linc00152 in view of prognosis, chemoresistance, genomic and epigenetic regulation, including DNA methylation and histone modification, potential biological function enrichment, and basic molecular function in pan-cancer, were also evaluated in vitro and in vivo. Results: Linc00152 is upregulated in pan-cancer, especially in progressive cancer, and the high expression of linc00152 may lead to a worse prognosis and chemoresistance in pan-cancer patients. Amplification, DNA hypomethylation, promoter-like lncRNA characteristics and super-enhancer regulation are the drivers that lead to the upregulation of linc00152 in pan-cancer. Meanwhile, linc00152 was involved in cancer-related pathways, infection and immune response-associated pathways by enriched analysis using TCGA data. Finally, linc00152 was confirmed to promote the proliferation, migration and invasion in MDA-MB-231, SGC-7901 and 786-O. Moreover, RIP and RNA pull-down assays indicated that linc00152 can bind to EZH2 directly. Conclusion: All of the results indicated that linc00152 acted as an oncogenic propellant from various perspectives, and it may be an effective therapy target in pan-cancer. (C) 2017 The Author(s) Published by S. Karger AG, Basel

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据