LncRNA NEAT1 promotes autophagy via regulating miR‐204/ATG3 and enhanced cell resistance to sorafenib in hepatocellular carcinoma. Issue 4 (23rd September 2019)

• Record Type: Journal Article
• Authors: Li, Xinyu; Zhou, Yong; Yang, Liang; Ma, Yingbo; Peng, Xueqiang; Yang, Shuo; Li, Hangyu; Liu, Jingang
• Is Part Of: Journal of cellular physiology. Volume 235:Issue 4(2020:Apr.)
• Page Start: 3402
• Page End: 3413
• Publication Date: 2019-09-23
• Subjects: autophagy -- HCC -- miRNA -- NEAT1 -- sorafenib; Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.29230
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: Long noncoding RNAs (lncRNAs) has been acknowledged in tumorigenesis gradually because of the great importance in different cancers. LncRNA nuclear enriched abundant transcript 1 (NEAT1) is a novel lncRNA and has been reported to promote multiple cancer progression. However, the biological roles of NEAT1 in hepatocellular carcinoma (HCC) is not cleared nowadays. In the present research, the level of NEAT1 was found to be upregulated in HCC by The Cancer Genome Atlas. In addition, NEAT1 expression is negatively correlated with the survival rate in HCC. Further investigation revealed that NEAT1 upregulation inhibited sorafenib efficacy and promoted autophagy. We found that NEAT1 could be a sponge for microRNA‐204 (miR‐204) and inhibits its level to upregulate ATG3 expression. In addition to the above, we demonstrated that miR‐204 mimics also attenuated tumor autophagy. And rescue assays demonstrated that NEAT1 promotes HCC autophagy through modulating miR‐204/ATG3 pathway. Collectively, this study first demonstrated that a novel NEAT1/miR‐204/ATG3 signaling regulates HCC progression. Abstract : Nuclear enriched abundant transcript 1 (NEAT1) could be a sponge for microRNA‐204 (miR‐204) and inhibits its level to upregulate ATG3 expression. We demonstrated that miR‐204 mimics also attenuated tumor autophagy. And rescue assays demonstrated that NEAT1 promotes hepatocellular carcinoma (HCC) autophagy through modulating miR‐204/ATG3 pathway.