lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation

Abstract Background Hepatocellular carcinoma (HCC) is one of the most malignant tumors to threaten human life, and the survival rate remains low due to delayed diagnosis. Meanwhile, lncRNAs have great potential for application in tumor prognosis, therefore relevant research in hepatocellular carcino...

Full description

Bibliographic Details
Main Authors: Xia-Hui Lin, Dan-Ying Zhang, Zhi-Yong Liu, Wen-qing Tang, Rong-Xin Chen, Dong-ping Li, Shuqiang Weng, Ling Dong
Format: Article
Language:English
Published: BMC 2022-08-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-022-03573-7
_version_ 1817994131239075840
author Xia-Hui Lin
Dan-Ying Zhang
Zhi-Yong Liu
Wen-qing Tang
Rong-Xin Chen
Dong-ping Li
Shuqiang Weng
Ling Dong
author_facet Xia-Hui Lin
Dan-Ying Zhang
Zhi-Yong Liu
Wen-qing Tang
Rong-Xin Chen
Dong-ping Li
Shuqiang Weng
Ling Dong
author_sort Xia-Hui Lin
collection DOAJ
description Abstract Background Hepatocellular carcinoma (HCC) is one of the most malignant tumors to threaten human life, and the survival rate remains low due to delayed diagnosis. Meanwhile, lncRNAs have great potential for application in tumor prognosis, therefore relevant research in hepatocellular carcinoma is indispensable. Methods Based on the EZH2 expression, the differentially expressed lncRNAs DElncRNAs), miRNAs (DEmiRNAs), and mRNAs (DEmRNAs) were identified in hepatocellular carcinoma by using the TCGA database. Bioinformatics technology was utilized to determine the effect of key genes in HCC progression. The methylation and immune infiltration analyses were performed to explore the underlying function of hub genes. Finally, cellular function experiments were performed to investigate the association between identified genes and biological phenotypes in HCC. Results lncRNA-AC079061.1, hsa-miR-765, and VIPR1 were identified as independent factors that affect the prognosis of hepatocellular carcinoma. The immune infiltration analyses revealed that lncRNA-AC079061.1 can alter the immune microenvironment and thus inhibit the development of HCC by regulating the expression of an immune-related gene (VIPR1). Methylation analyses demonstrated that VIPR1 expression is negatively related to the methylation level in HCC. Experimental results suggested that lncRNA-AC079061.1 and VIPR1 were frequently downregulated in HCC cells, while hsa-miR-765 was significantly upregulated. Moreover, the lncRNA-AC079061.1/VIPR1 axis suppressed the proliferation and invasion of HCC cells. Conclusion The present study identified the lncRNA-AC079061.1/VIPR1 axis as a novel biomarker that inhibited the proliferation and invasion of hepatocellular carcinoma, affecting the ultimate disease outcome.
first_indexed 2024-04-14T01:47:48Z
format Article
id doaj.art-8b64c4a6816443fcae9304f11125709a
institution Directory Open Access Journal
issn 1479-5876
language English
last_indexed 2024-04-14T01:47:48Z
publishDate 2022-08-01
publisher BMC
record_format Article
series Journal of Translational Medicine
spelling doaj.art-8b64c4a6816443fcae9304f11125709a2022-12-22T02:19:27ZengBMCJournal of Translational Medicine1479-58762022-08-0120112110.1186/s12967-022-03573-7lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validationXia-Hui Lin0Dan-Ying Zhang1Zhi-Yong Liu2Wen-qing Tang3Rong-Xin Chen4Dong-ping Li5Shuqiang Weng6Ling Dong7Department of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityLiver Cancer Institute, Zhongshan Hospital, Fudan University and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of EducationDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityDepartment of Gastroenterology and Hepatology, Zhongshan Hospital, Fudan UniversityAbstract Background Hepatocellular carcinoma (HCC) is one of the most malignant tumors to threaten human life, and the survival rate remains low due to delayed diagnosis. Meanwhile, lncRNAs have great potential for application in tumor prognosis, therefore relevant research in hepatocellular carcinoma is indispensable. Methods Based on the EZH2 expression, the differentially expressed lncRNAs DElncRNAs), miRNAs (DEmiRNAs), and mRNAs (DEmRNAs) were identified in hepatocellular carcinoma by using the TCGA database. Bioinformatics technology was utilized to determine the effect of key genes in HCC progression. The methylation and immune infiltration analyses were performed to explore the underlying function of hub genes. Finally, cellular function experiments were performed to investigate the association between identified genes and biological phenotypes in HCC. Results lncRNA-AC079061.1, hsa-miR-765, and VIPR1 were identified as independent factors that affect the prognosis of hepatocellular carcinoma. The immune infiltration analyses revealed that lncRNA-AC079061.1 can alter the immune microenvironment and thus inhibit the development of HCC by regulating the expression of an immune-related gene (VIPR1). Methylation analyses demonstrated that VIPR1 expression is negatively related to the methylation level in HCC. Experimental results suggested that lncRNA-AC079061.1 and VIPR1 were frequently downregulated in HCC cells, while hsa-miR-765 was significantly upregulated. Moreover, the lncRNA-AC079061.1/VIPR1 axis suppressed the proliferation and invasion of HCC cells. Conclusion The present study identified the lncRNA-AC079061.1/VIPR1 axis as a novel biomarker that inhibited the proliferation and invasion of hepatocellular carcinoma, affecting the ultimate disease outcome.https://doi.org/10.1186/s12967-022-03573-7Hepatocellular carcinoma (HCC)ceRNA mechanismBioinformatics analysisProliferationInvasionPrognosis
spellingShingle Xia-Hui Lin
Dan-Ying Zhang
Zhi-Yong Liu
Wen-qing Tang
Rong-Xin Chen
Dong-ping Li
Shuqiang Weng
Ling Dong
lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
Journal of Translational Medicine
Hepatocellular carcinoma (HCC)
ceRNA mechanism
Bioinformatics analysis
Proliferation
Invasion
Prognosis
title lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
title_full lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
title_fullStr lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
title_full_unstemmed lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
title_short lncRNA-AC079061.1/VIPR1 axis may suppress the development of hepatocellular carcinoma: a bioinformatics analysis and experimental validation
title_sort lncrna ac079061 1 vipr1 axis may suppress the development of hepatocellular carcinoma a bioinformatics analysis and experimental validation
topic Hepatocellular carcinoma (HCC)
ceRNA mechanism
Bioinformatics analysis
Proliferation
Invasion
Prognosis
url https://doi.org/10.1186/s12967-022-03573-7
work_keys_str_mv AT xiahuilin lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT danyingzhang lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT zhiyongliu lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT wenqingtang lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT rongxinchen lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT dongpingli lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT shuqiangweng lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation
AT lingdong lncrnaac0790611vipr1axismaysuppressthedevelopmentofhepatocellularcarcinomaabioinformaticsanalysisandexperimentalvalidation