| Literature DB >> 27929737 |
Tao Li1, Xiao-Dong Yang1, Chun-Xiang Ye1, Zhan-Long Shen1, Yang Yang1, Bo Wang1, Peng Guo1, Zhi-Dong Gao1, Ying-Jiang Ye1, Ke-Wei Jiang1, Shan Wang1.
Abstract
Accumulating evidence suggests that long noncoding RNAs (lncRNAs) play an important role in oncogenesis and tumor progression. However, our knowledge of lncRNAs in thyroid cancer is still limited. To explore the crucial lncRNAs involved in oncogenesis of papillary thyroid cancer (PTC), we acquired data of differentially expressed lncRNAs between PTC tissues and paired adjacent noncancerous thyroid tissues through lncRNA microarray. In the microarray data, we observed that a newly identified lncRNA, HIT000218960, was significantly upregulated in PTC tissues and associated with a well-known oncogene, high mobility group AT-hook 2 (HMGA2) gene. Both in normal thyroid tissues and PTC tissues, the expression of HIT000218960 was significantly positively correlated with that of HMGA2 mRNA. Knockdown of HIT000218960 in PTC cells resulted in downregulation of HMGA2. In addition, functional assays indicated that inhibition of HIT000218960 in PTC cells suppressed cell proliferation, colony formation, migration and invasion in vitro. Increased HIT000218960 expression in PTC tissues was obviously correlated with lymph node metastasis and multifocality, as well as TNM stage. Those findings suggest that HIT000218960 might acts as a tumor promoter through regulating the expression of HMGA2.Entities:
Keywords: HIT000218960; HMGA2; long noncoding RNA; oncogenesis; papillary thyroid cancer
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Year: 2016 PMID: 27929737 PMCID: PMC5283824 DOI: 10.1080/15384101.2016.1261768
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534