Identification of differentially expressed genes in non-small cell lung cancer

被引:31
作者
Wang, Ke [1 ,2 ]
Chen, Ruo [1 ,2 ]
Feng, Zhuan [1 ,2 ]
Zhu, Yu-Meng [1 ,2 ]
Sun, Xiu-Xuan [1 ,2 ]
Huang, Wan [1 ,2 ]
Chen, Zhi-Nan [1 ,2 ]
机构
[1] Fourth Mil Med Univ, Natl Translat Sci Ctr Mol Med, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Dept Cell Biol, Xian 710032, Shaanxi, Peoples R China
来源
AGING-US | 2019年 / 11卷 / 23期
基金
中国国家自然科学基金;
关键词
NSCLC; bioinformatics; biomarkers; TOP2A; WEB SERVER; II-ALPHA; CARCINOMA; MARKER; GLUCOSE-TRANSPORTER-1; APOPTOSIS; ASPM;
D O I
10.18632/aging.102521
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung cancer is the most common malignant tumor and the leading cause of cancer-related deaths worldwide. Because current treatments for advanced non-small cell lung cancer (NSCLC), the most prevalent lung cancer histological subtype, show limited efficacy, screening for tumor-associated biomarkers using bioinformatics reflects the hope to improve early diagnosis and prognosis assessment. In our study, a Gene Expression Omnibus dataset was analyzed to identify genes with prognostic significance in NSCLC. Upon comparison with matched normal tissues, 118 differentially expressed genes (DEGs) were identified in NSCLC, and their functions were explored through bioinformatics analyses. The most significantly upregulated DEGs were TOP2A, SLC2A1, TPX2, and ASPM, all of which were significantly associated with poor overall survival (OS). Further analysis revealed that TOP2A had prognostic significance in early-stage lung cancer patients, and its expression correlated with levels of immune cell infiltration, especially dendritic cells (DCs). Our study provides a dataset of potentially prognostic NSCLC biomarkers, and highlights TOP2A as a valuable survival biomarker to improve prediction of prognosis in NSCLC.
引用
收藏
页码:11170 / 11185
页数:16
相关论文
共 42 条
[1]   Regulatory T-cell Genes Drive Altered Immune Microenvironment in Adult Solid Cancers and Allow for Immune Contextual Patient Subtyping [J].
Brouwer-Visser, Jurriaan ;
Cheng, Wei-Yi ;
Bauer-Mehren, Anna ;
Maisel, Daniela ;
Lechner, Katharina ;
Andersson, Emilia ;
Dudley, Joel T. ;
Milletti, Francesca .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2018, 27 (01) :103-112
[2]   Biomarkers in Early-Stage Non-Small-Cell Lung Cancer Current Concepts and Future Directions [J].
Burotto, Mauricio ;
Thomas, Anish ;
Subramaniam, Deepa ;
Giaccone, Giuseppe ;
Rajan, Arun .
JOURNAL OF THORACIC ONCOLOGY, 2014, 9 (11) :1609-1617
[3]   Identification of Novel MicroRNAs and Their Diagnostic and Prognostic Significance in Oral Cancer [J].
Falzone, Luca ;
Lupo, Gabriella ;
La Rosa, Giusy Rita Maria ;
Crimi, Salvatore ;
Anfuso, Carmelina Daniela ;
Salemi, Rossella ;
Rapisarda, Ernesto ;
Libra, Massimo ;
Candido, Saverio .
CANCERS, 2019, 11 (05)
[4]   Role of glucose metabolism related gene GLUT1 in the occurrence and prognosis of colorectal cancer [J].
Feng, Wenming ;
Cui, Ge ;
Tang, Cheng-Wu ;
Zhang, Xiao-Lan ;
Dai, Chuang ;
Xu, Yong-Qiang ;
Gong, Hui ;
Xue, Tao ;
Guo, Hui-Hui ;
Bao, Ying .
ONCOTARGET, 2017, 8 (34) :56850-56857
[5]   Online Survival Analysis Software to Assess the Prognostic Value of Biomarkers Using Transcriptomic Data in Non-Small-Cell Lung Cancer [J].
Gyorffy, Balazs ;
Surowiak, Pawel ;
Budczies, Jan ;
Lanczky, Andras .
PLOS ONE, 2013, 8 (12)
[6]  
Haber RS, 1998, CANCER, V83, P34, DOI 10.1002/(SICI)1097-0142(19980701)83:1<34::AID-CNCR5>3.0.CO
[7]  
2-E
[8]  
Hanagiri Takeshi, 2011, Journal of UOEH, V33, P205
[9]   Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources [J].
Huang, Da Wei ;
Sherman, Brad T. ;
Lempicki, Richard A. .
NATURE PROTOCOLS, 2009, 4 (01) :44-57
[10]   Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists [J].
Huang, Da Wei ;
Sherman, Brad T. ;
Lempicki, Richard A. .
NUCLEIC ACIDS RESEARCH, 2009, 37 (01) :1-13