Establishment of an endoplasmic reticulum stress-associated lncRNAs model to predict prognosis and immunological characteristics in hepatocellular carcinoma

被引:4
作者
Shen, Xingyuan [1 ]
Wu, Siyuan [2 ]
Yang, Zhen [1 ]
Zhu, Chunfu [2 ]
机构
[1] Dalian Med Univ, Sch Grad, Dalian, Liaoning, Peoples R China
[2] Nanjing Med Univ, Affiliated Changzhou Peoples Hosp 2, Dept Gen Surg, Changzhou, Peoples R China
关键词
UNFOLDED PROTEIN RESPONSE; MACROPHAGES; DISCOVERY; CELLS; TOOL;
D O I
10.1371/journal.pone.0287724
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
BackgroundThe endoplasmic reticulum stress (ERS) and unfolded protein response (UPR) pathways play an essential role in the pathophysiology of hepatocellular carcinoma (HCC), and activation of the UPR pathway is strongly associated with tumor growth. However, the function of ERS-associated long non-coding RNAs (lncRNAs) in HCC is less recognized.MethodsWe have used TCGA (The Cancer Genome Atlas) to obtain clinical and transcriptome data for HCC patients and the GSEA (Gene Set Enrichment Analysis) molecular signature database to get the ERS gene. ERS-associated prognostic lncRNA was determined using univariate Cox regression study. Then, least absolute shrinkage and selection operator and multivariate Cox regression study were used to construct ERS-associated lncRNAs risk model. Next, we use Kaplan-Meier (KM) survival study, time-dependent receiver operating characteristic (ROC) curve, univariate and multivariate Cox regression study to validate and evaluate the risk model. GSEA reveals the underlying molecular mechanism of the risk model. In addition, differences in Immune cell Infiltration Study, half-maximal inhibitory concentration (IC50) and immune checkpoints blockade (ICB) treatment between high and low risk groups were analyzed.ResultsWe constructed a risk model consisting of 6 ERS-associated lncRNAS (containingMKLN1-AS, LINC01224, AL590705.3, AC008622.2, AC145207.5, and AC026412.3). The KM survival study showed that the prognosis of HCC patients in low-risk group was better than that in high-risk group. ROC study, univariate and multivariate Cox regression study showed that the risk model had good predictive power for HCC patients. Our verification sample verified the aforesaid findings. GSEA suggests that several tumor- and metabolism-related signaling pathways are associated with risk groups. Simultaneously, we discovered that the risk models may help in the treatment of ICB and the selection of chemotherapeutic drugs.ConclusionsIn this article, we created an ERS-associated lncRNAs risk model to help prognostic diagnosis and personalized therapy in HCC.
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页数:18
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共 50 条
[1]   Regulatory T cells in cancer [J].
Beyer, Marc ;
Schultze, Joachim L. .
BLOOD, 2006, 108 (03) :804-811
[2]   Long Noncoding RNA and Cancer: A New Paradigm [J].
Bhan, Arunoday ;
Soleimani, Milad ;
Mandal, Subhrangsu S. .
CANCER RESEARCH, 2017, 77 (15) :3965-3981
[3]   BTK Has Potential to Be a Prognostic Factor for Lung Adenocarcinoma and an Indicator for Tumor Microenvironment Remodeling: A Study Based on TCGA Data Mining [J].
Bi, Ke-Wei ;
Wei, Xu-Ge ;
Qin, Xiao-Xue ;
Li, Bo .
FRONTIERS IN ONCOLOGY, 2020, 10
[4]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[5]   Endoplasmic reticulum stress signals in the tumour and its microenvironment [J].
Chen, Xi ;
Cubillos-Ruiz, Juan R. .
NATURE REVIEWS CANCER, 2021, 21 (02) :71-88
[6]   Membrane phospholipid synthesis and endoplasmic reticulum function [J].
Fagone, Paolo ;
Jackowski, Suzanne .
JOURNAL OF LIPID RESEARCH, 2009, 50 :S311-S316
[7]   Simvastatin re-sensitizes hepatocellular carcinoma cells to sorafenib by inhibiting HIF-1α/PPAR-γ/PKM2-mediated glycolysis [J].
Feng, Jiao ;
Dai, Weiqi ;
Mao, Yuqing ;
Wu, Liwei ;
Li, Jingjing ;
Chen, Kan ;
Yu, Qiang ;
Kong, Rui ;
Li, Sainan ;
Zhang, Jie ;
Ji, Jie ;
Wu, Jianye ;
Mo, Wenhui ;
Xu, Xuanfu ;
Guo, Chuanyong .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2020, 39 (01)
[8]   Hepatocellular carcinoma [J].
Forner, Alejandro ;
Reig, Maria ;
Bruix, Jordi .
LANCET, 2018, 391 (10127) :1301-1314
[9]   Progress and prospects of biomarkers in primary liver cancer (Review) [J].
Gao, Yu-Xue ;
Yang, Tong-Wang ;
Yin, Ji-Ming ;
Yang, Peng-Xiang ;
Kou, Bu-Xin ;
Chai, Meng-Yin ;
Liu, Xiao-Ni ;
Chen, De-Xi .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2020, 57 (01) :54-66
[10]   pRRophetic: An R Package for Prediction of Clinical Chemotherapeutic Response from Tumor Gene Expression Levels [J].
Geeleher, Paul ;
Cox, Nancy ;
Huang, R. Stephanie .
PLOS ONE, 2014, 9 (09)