Linc00511 Indicates A Poor Prognosis Of Liver Hepatocellular Carcinoma
Authors Hu P, Cui H, Lei T, Li S, Mai E, Jia F
Received 22 August 2019
Accepted for publication 18 October 2019
Published 8 November 2019 Volume 2019:12 Pages 9367—9376
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Shashank Kaushik (PT)
Peer reviewer comments 2
Editor who approved publication: Dr Sanjeev Srivastava
Pingan Hu,1 Huxiao Cui,2 Ting Lei,1 Siqiao Li,1 Erhui Mai,1 Fuxin Jia1
1Department of Hepatobiliary Surgery, Luoyang Center Hospital, Luoyang, People’s Republic of China; 2Department of Hepatobiliary Surgery, Xuchang Central Hospital, Xuchang, People’s Republic of China
Correspondence: Pingan Hu
Department of Hepatobiliary Surgery, Luoyang Center Hospital, No. 288, Zhongzhou Middle Road, Xigong District, Luoyang, Henan 471000, People’s Republic of China
Objective: To uncover the specific function of linc00511 in the progression of liver hepatocellular carcinoma (LIHC) and the underlying mechanism.
Patients and methods: GEPIA dataset containing 9736 LIHC samples and 857 normal samples were downloaded from TCGA. Expression pattern and prognostic potential of linc00511 in LIHC were analyzed. Subsequently, expression level of linc00511 in LIHC tissues collected in our hospital and cell lines were determined by quantitative real-time polymerase chain reaction (qRT-PCR). Differential expressions of linc00511 in LIHC with different tumor grades and metastatic status were compared. After transfection of si-linc00511, proliferative and migratory changes in Huh7 and Hep3B cells were assessed by cell counting kit-8 (CCK-8), 5-ethynyl-2ʹ-deoxyuridine (EdU) and Transwell assay. Lastly, Pearson correlation analysis and qRT-PCR were conducted to investigate the interaction between linc00511 and miR-29c.
Results: Linc00511 was upregulated in LIHC tissues and cell lines. Its level was positively correlated to TNM staging, lymphatic metastasis and poor prognosis in LIHC patients. Knockdown of linc00511 attenuated proliferative and migratory abilities in Huh7 and Hep3B cells. In addition, miR-29c was downregulated in LIHC and negatively linked to linc00511 level. A negative interaction between linc00511 and miR-29c could be a regulatory feedback influencing the progression of LIHC.
Conclusion: Linc00511 accelerates the proliferation and migration in LIHC, thus aggravating tumor progression. Meanwhile, linc00511 could be utilized as a hallmark predicting poor prognosis in LIHC patients.
Keywords: LIHC, linc00511, miRNA-29c, proliferation, migration
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