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长链非编码RNA ST8SIA6-AS1通过调控miR-142-3p促进肝癌的增殖和侵袭。

lncRNA ST8SIA6-AS1 facilitates proliferation and invasion in liver cancer by regulating miR-142-3p.

作者信息

Zhang Yang, Yang Yan, Zhang Yi, Liu Zhisu

机构信息

Department of General Surgery, The General Hospital of The Central Military Theater of The People's Liberation Army, Wuhan, Hubei 430030, P.R. China.

Department of Pediatric Hematology, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430031, P.R. China.

出版信息

Exp Ther Med. 2021 Dec;22(6):1348. doi: 10.3892/etm.2021.10783. Epub 2021 Sep 23.

Abstract

Long non-coding RNA ST8 α-N-acetyl-neuraminide α-2,8-sialyltransferase 6 antisense 1 (ST8SIA6-AS1) has been identified as a novel oncogene in breast cancer. However, its involvement in liver cancer has remained elusive. In the present study, the expression of ST8SIA6-AS1 and microRNA (miR)-142-3p in liver cancer tissues and cell lines was detected by reverse transcription-quantitative PCR. Tumor cell proliferation, migration and invasion assays were performed to determine the biological functions of ST8SIA6-AS1. The targeting interaction between ST8SIA6-AS1 and miR-142-3p predicted by bioinformatics was verified by a luciferase reporter assay and a biotin pulldown assay. The results indicated that ST8SIA6-AS1 was highly expressed in liver cancer tissues and cell lines, and the high expression of ST8SIA6-AS1 in liver cancer tissues was associated with poor prognosis. Knockdown of ST8SIA6-AS1 inhibited the proliferation, metastasis and invasion of liver cancer cells. Mechanistic investigation revealed that ST8SIA6-AS1 sequesters miR-142-3p and negatively regulates miR-142-3p expression in liver cancer cells. Further investigation indicated that the tumor-inhibitory effect of ST8SIA6-AS1 silencing was reversed by miR-142-3p depletion. In conclusion, ST8SIA6-AS1 was indicated to exert an oncogenic function in liver cancer by competitively sponging miR-142-3p.

摘要

长链非编码RNA ST8 α-N-乙酰神经氨酸α-2,8-唾液酸转移酶6反义1(ST8SIA6-AS1)已被确定为乳腺癌中的一种新型致癌基因。然而,其在肝癌中的作用仍不明确。在本研究中,通过逆转录定量PCR检测了肝癌组织和细胞系中ST8SIA6-AS1和微小RNA(miR)-142-3p的表达。进行肿瘤细胞增殖、迁移和侵袭实验以确定ST8SIA6-AS1的生物学功能。通过荧光素酶报告基因实验和生物素下拉实验验证了生物信息学预测的ST8SIA6-AS1与miR-142-3p之间的靶向相互作用。结果表明,ST8SIA6-AS1在肝癌组织和细胞系中高表达,且肝癌组织中ST8SIA6-AS1的高表达与预后不良相关。敲低ST8SIA6-AS1可抑制肝癌细胞的增殖、转移和侵袭。机制研究表明,ST8SIA6-AS1在肝癌细胞中可隔离miR-142-3p并负向调节miR-142-3p的表达。进一步研究表明,miR-142-3p缺失可逆转ST8SIA6-AS1沉默的肿瘤抑制作用。总之,ST8SIA6-AS1通过竞争性结合miR-142-3p在肝癌中发挥致癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3de/8515546/7bfaa54681fe/etm-22-06-10783-g00.jpg

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