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lncRNA SLC16A1-AS1 as a novel prognostic biomarker in non-small cell lung cancer.

Authors :
Hong Yue Liu
Sheng Rong Lu
Zi Han Guo
Zhi Sheng Zhang
Xuan Ye
Qiong Du
Huan Li
Qiang Wu
Bo Yu
Qing Zhai
Jin Long Liu
Liu, Hong Yue
Lu, Sheng Rong
Guo, Zi Han
Zhang, Zhi Sheng
Ye, Xuan
Du, Qiong
Li, Huan
Wu, Qiang
Yu, Bo
Source :
Journal of Investigative Medicine (Sage Publications Inc.); Jan2020, Vol. 68 Issue 1, p52-59, 8p
Publication Year :
2020

Abstract

Long non-coding RNAs (lncRNAs) have proved to act as crucial biomarkers in tumors. Novel biomarkers in non-small cell lung cancer (NSCLC) need to be investigated badly. To identify the differentially expressed lncRNAs between NSCLC tissue and adjacent tissue, microarray analysis was performed. lncRNA SLC16A1-AS1 was significantly less expressed in NSCLC tissue than that in adjacent tissue. Gain-of-function experiments was performed to determine the biological functions of SLC16A1-AS. In situhybridization and survival analysis were applied in lung cancer tissue samples to determine the prognostic role of SLC16A1-AS1. It was showed that SLC16A1-AS1 was remarkably downregulated in NSCLC tissues and cell lines. Functionally, SLC16A1-AS1 overexpression could inhibit the viability and proliferation of lung cancer cell, block the cell cycle and promote cell apoptosis in vitro which may result from reduced phosphorylation of rat sarcoma (RAS)/ proto-oncogene serine/threonine-protein kinase (RAF)/ mitogen-activated protein kinase kinase (MEK)/ extracellular regulated protein kinases (ERK) pathway caused by elevated expression of SLC16A1-AS1. Clinical sample analysis showed that SLC16A1-AS1 had a favorable impact on the overall survival and progression-free survival of patients with NSCLC. Our results suggested that SLC16A1-AS1 may act as a potential biomarker for patients with NSCLC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10815589
Volume :
68
Issue :
1
Database :
Complementary Index
Journal :
Journal of Investigative Medicine (Sage Publications Inc.)
Publication Type :
Academic Journal
Accession number :
148134688
Full Text :
https://doi.org/10.1136/jim-2019-001080