| Literature DB >> 29735546 |
Qiheng Gou1,2, Linbo Gao3, Xinwen Nie4, Wenchen Pu1, Jingqiang Zhu5, Yichao Wang5, Xuesha Liu1, Shuangyan Tan1, Jian-Kang Zhou1, Yanqiu Gong1, Juan He1, Ke Wu1, Yuxin Xie1, Wanjun Zhao5, Lunzhi Dai1, Lunxu Liu1, Rong Xiang6, Yu-Quan Wei1, Lin Zhang7, Yong Peng8.
Abstract
Long noncoding RNAs (lncRNA) are emerging as a novel class of regulators in gene expression associated with tumorigenesis. However, the role of lncRNAs in papillary thyroid carcinoma (PTC) is poorly understood. Here, we conducted global lncRNA profiling and identified lncRNA AB074169 (lncAB) as significantly downregulated in PTC. Decreased expression of lncAB in PTC was caused by CpG hypermethylation within its gene promoter. Functional studies showed that lncAB overexpression led to cell-cycle arrest and tumor growth inhibition in vitro and in vivo, whereas lncAB knockdown promoted cell proliferation. Mechanistic analyses revealed that lncAB bound KH-type splicing regulatory protein (KHSRP) and also decreased expression of KHSRP, thus increasing CDKN1a (p21) expression and decreasing CDK2 expression to repress cell proliferation. Taken together, these findings demonstrate that lncAB functions as a tumor suppressor during PTC tumorigenesis.Significance: These findings identify a tumor-suppressive long noncoding RNA in papillary thyroid carcinoma.Graphical Abstract: http://cancerres.aacrjournals.org/content/canres/78/15/4163/F1.large.jpg Cancer Res; 78(15); 4163-74. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29735546 DOI: 10.1158/0008-5472.CAN-17-3766
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701