Prognostic Ability of Enhancer RNAs in Metastasis of Non-Small Cell Lung Cancer

被引:5
作者
Liu, Jun [1 ,2 ]
Jia, Jingyi [1 ,2 ,3 ,4 ]
Wang, Siqiao [2 ]
Zhang, Junfang [2 ]
Xian, Shuyuan [2 ]
Zheng, Zixuan [2 ]
Deng, Lin [5 ]
Feng, Yonghong [2 ,3 ,4 ]
Zhang, Yuan [6 ]
Zhang, Jie [1 ,2 ]
机构
[1] Shanghai Pulm Hosp, Tongji Univ, Dept Anesthesiol, Sch Med, Shanghai 200433, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai 200092, Peoples R China
[3] Shanghai Pulm Hosp, Tongji Univ, Shanghai Key Lab TB, Sch Med, Shanghai 200433, Peoples R China
[4] Tongji Univ, Shanghai Pulm Hosp, Sch Med, Shanghai Clin Res Ctr Infect Dis Tuberculosis, Shanghai 200433, Peoples R China
[5] Qingdao Univ, Normal Coll, Qingdao 266071, Peoples R China
[6] Shanghai Pulm Hosp, Tongji Univ, Dept Pulm & Crit Care Med, Sch Med, Shanghai 200433, Peoples R China
关键词
Non-small cell lung cancer; metastasis; enhancer RNAs; regulatory network; prognosis; GENE-EXPRESSION; CHROMATIN ACCESSIBILITY; CONNECTIVITY MAP; DENDRITIC CELLS; CHIP-SEQ; TRANSCRIPTION; EPIDEMIOLOGY; PROLIFERATION; METABOLISM; GLYCOLYSIS;
D O I
10.3390/molecules27134108
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
(1) Background: Non-small cell lung cancer (NSCLC) is the most common lung cancer. Enhancer RNA (eRNA) has potential utility in the diagnosis, prognosis and treatment of cancer, but the role of eRNAs in NSCLC metastasis is not clear; (2) Methods: Differentially expressed transcription factors (DETFs), enhancer RNAs (DEEs), and target genes (DETGs) between primary NSCLC and metastatic NSCLC were identified. Prognostic DEEs (PDEEs) were screened by Cox regression analyses and a predicting model for metastatic NSCLC was constructed. We identified DEE interactions with DETFs, DETGs, reverse phase protein arrays (RPPA) protein chips, immunocytes, and pathways to construct a regulation network using Pearson correlation. Finally, the mechanisms and clinical significance were explained using multi-dimensional validation unambiguously; (3) Results: A total of 255 DEEs were identified, and 24 PDEEs were selected into the multivariate Cox regression model (AUC = 0.699). Additionally, the NSCLC metastasis-specific regulation network was constructed, and six key PDEEs were defined (ANXA8L1, CASTOR2, CYP4B1, GTF2H2C, PSMF1 and TNS4); (4) Conclusions: This study focused on the exploration of the prognostic value of eRNAs in the metastasis of NSCLC. Finally, six eRNAs were identified as potential markers for the prediction of metastasis of NSCLC.
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页数:25
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