NCF1/2/4 Are Prognostic Biomarkers Related to the Immune Infiltration of Kidney Renal Clear Cell Carcinoma

被引:18
作者
Chen, Yifei [1 ]
He, Fei [2 ]
Wang, Ruhua [1 ]
Yao, Menglin [1 ]
Li, Yarui [1 ]
Guo, Dan [1 ]
He, Shuixiang [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Gastroenterol, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Dept Urol, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
关键词
SYSTEMIC THERAPY; GENE-EXPRESSION; CANCER; PROMOTE; SERVER;
D O I
10.1155/2021/5954036
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Neutrophil cytoplasmic factor 1/2/4 (NCF1/2/4) belongs to the NADPH oxidase complex, which is a cytoplasmic component, and its polymorphism is the main factor related to autoimmune diseases, which is probably caused by the regulation of peroxide. They also play a role in tumor growth and metastasis. This research is aimed at evaluating the biological function and prognostic role of NCF1, NCF2, and NCF4 genes in kidney renal clear cell carcinoma (KIRC) by using multiple online bioinformatics website, including Oncomine, GEPIA, UALCAN, Kaplan-Meier Plotter, TIMER, TISIDB, cBioPortal, LinkedOmics, GeneMANIA, and DAVID databases. The mRNA levels of NCFs were higher in KIRC tissues than in normal tissues. The overexpression of NCFs was significantly correlated with advanced pathological grades and individual cancer stages in KIRC. Meanwhile, the expressions of NCFs played an important role in the tumorigenesis and progression of KIRC. Prognostic value analysis suggested that high transcription levels of NCF1/4 were associated with poor overall survival in KIRC patients. In addition, results from the LinkedOmics database showed that the KEGG pathway related to NCFs mainly focused on immune activation and immune regulation function. NCF genetic alterations, including copy number amplification, missense mutation, and deep deletion, could be found through the cBioPortal database. Further, NCF expression was significantly correlated with infiltration levels of various immune cells as well as immune signatures. Protein-protein interaction network and enrichment analysis of NCF1/2/4 in KIRC showed that NCF coexpressed genes mainly associated with diverse immune marker sets showed significance. Overall, these results indicated that NCFs could be prognostic biomarkers as well as effective targets for diagnosis in KIRC.
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页数:31
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[1]   EMT, MET, Plasticity, and Tumor Metastasis [J].
Bakir, Basil ;
Chiarella, Anna M. ;
Pitarresi, Jason R. ;
Rustgi, Anil K. .
TRENDS IN CELL BIOLOGY, 2020, 30 (10) :764-776
[2]   UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses [J].
Chandrashekar, Darshan S. ;
Bashel, Bhuwan ;
Balasubramanya, Sai Akshaya Hodigere ;
Creighton, Chad J. ;
Ponce-Rodriguez, Israel ;
Chakravarthi, Balabhadrapatruni V. S. K. ;
Varambally, Sooryanarayana .
NEOPLASIA, 2017, 19 (08) :649-658
[3]   Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects [J].
Chiriaco, Maria ;
Salfa, Irene ;
Di Matteo, Gigliola ;
Rossi, Paolo ;
Finocchi, Andrea .
PEDIATRIC ALLERGY AND IMMUNOLOGY, 2016, 27 (03) :242-253
[4]   Evaluation of ITGB2 (CD18) and SELL (CD62L) genes expression and methylation of ITGB2 promoter region in patients with systemic sclerosis [J].
Dashti, Navid ;
Mahmoudi, Mahdi ;
Gharibdoost, Farhad ;
Kavosi, Hoda ;
Rezaei, Ramazan ;
Imeni, Vahideh ;
Jamshidi, Ahmadreza ;
Aslani, Saeed ;
Mostafaei, Shayan ;
Vodjgani, Mohammad .
RHEUMATOLOGY INTERNATIONAL, 2018, 38 (03) :489-498
[5]   Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease [J].
Denson, Lee A. ;
Jurickova, Ingrid ;
Karns, Rebekah ;
Shaw, Kelly A. ;
Cutler, David J. ;
Okou, David T. ;
Dodd, Anne ;
Quinn, Kathryn ;
Mondal, Kajari ;
Aronow, Bruce J. ;
Haberman, Yael ;
Linn, Aaron ;
Price, Adam ;
Bezold, Ramona ;
Lake, Kathleen ;
Jackson, Kimberly ;
Walters, Thomas D. ;
Griffiths, Anne ;
Baldassano, Robert N. ;
Noe, Joshua D. ;
Hyams, Jeffrey S. ;
Crandall, Wallace V. ;
Kirschner, Barbara S. ;
Heyman, Melvin B. ;
Snapper, Scott ;
Guthery, Stephen L. ;
Dubinsky, Marla C. ;
Leleiko, Neal S. ;
Otley, Anthony R. ;
Xavier, Ramnik J. ;
Stevens, Christine ;
Daly, Mark J. ;
Zwick, Michael E. ;
Kugathasan, Subra .
GASTROENTEROLOGY, 2018, 154 (08) :2097-2110
[6]   The immunology of renal cell carcinoma [J].
Diaz-Montero, C. Marcela ;
Rini, Brian I. ;
Finke, James H. .
NATURE REVIEWS NEPHROLOGY, 2020, 16 (12) :721-735
[7]   Reactive oxygen species and cancer paradox: To promote or to suppress? [J].
Galadari, Sehamuddin ;
Rahman, Anees ;
Pallichankandy, Siraj ;
Thayyullathil, Faisal .
FREE RADICAL BIOLOGY AND MEDICINE, 2017, 104 :144-164
[8]   Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal [J].
Gao, Jianjiong ;
Aksoy, Buelent Arman ;
Dogrusoz, Ugur ;
Dresdner, Gideon ;
Gross, Benjamin ;
Sumer, S. Onur ;
Sun, Yichao ;
Jacobsen, Anders ;
Sinha, Rileen ;
Larsson, Erik ;
Cerami, Ethan ;
Sander, Chris ;
Schultz, Nikolaus .
SCIENCE SIGNALING, 2013, 6 (269) :pl1
[9]   Hodgkin-Reed-Sternberg Cells in Classical Hodgkin Lymphoma Show Alterations of Genes Encoding the NADPH Oxidase Complex and Impaired Reactive Oxygen Species Synthesis Capacity [J].
Giefing, Maciej ;
Winoto-Morbach, Supandi ;
Sosna, Justyna ;
Doering, Claudia ;
Klapper, Wolfram ;
Kueppers, Ralf ;
Boettcher, Sebastian ;
Adam, Dieter ;
Siebert, Reiner ;
Schuetze, Stefan .
PLOS ONE, 2013, 8 (12)
[10]  
GILLON G, 1988, EUR UROL, V14, P391