Identification of a Gene-Related Risk Signature in Melanoma Patients Using Bioinformatic Profiling

• Published in: Journal of oncology Vol. 2020; no. 2020; pp. 1 - 13
• Main Authors: Kong, Xin, Chen, Zong-Ke, Chen, Jing-Jing, Li, Chuan-Ying, Shao, Jian-Yong, Li, Ming, Weng, Hai-Yan, Zhou, Hang-Cheng, Wu, Wen-Qing, Song, Di, Wang, Hai-Yun, Kong, Peng-Fei, Wang, Jing, Meng, Bo
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 2020; Hindawi; John Wiley & Sons, Inc; Hindawi Limited
• Subjects: Cancer; Gene expression; Genes; Genetic aspects; Genomes; Genomics; Immunotherapy; Medical prognosis; Medical research; Medicine, Experimental; Melanoma; Metastasis; Patients; Prognosis; Regression analysis; Software; China
• ISSN: 1687-8450; 1687-8450; 1687-8469
• DOI: 10.1155/2020/7526204

Introduction. Gene signature has been used to predict prognosis in melanoma patients. Meanwhile, the efficacy of immunotherapy was correlated with particular genes expression or mutation. In this study, we systematically explored the gene expression pattern in the melanoma-immune microenvironment and its relationship with prognosis. Methods. A cohort of 122 melanoma cases with whole-genome microarray expression data were enrolled from the Gene Expression Omnibus (GEO) database. The findings were validated using The Cancer Genome Atlas (TCGA) database. A principal component analysis (PCA), gene set enrichment analysis (GSEA), and gene oncology (GO) analysis were performed to explore the bioinformatic implications. Results. Different gene expression patterns were identified according to the clinical stage. All eligible gene sets were analyzed, and the 8 genes (GPR87, KIT, SH3GL3, PVRL1, ATP1B1, CDAN1, FAU, and TNFSF14) with the greatest prognostic impact on melanoma. A gene-related risk signature was developed to distinguish patients with a high or low risk of an unfavorable outcome, and this signature was validated using the TCGA database. Furthermore, the prognostic significance of the signature between the classified subgroups was verified as an independent prognostic predictor of melanoma. Additionally, the low-risk melanoma patients presented an enhanced immune phenotype compared to that of the high-risk gene signature patients. Conclusions. The gene pattern differences in melanoma were profiled, and a gene signature that could independently predict melanoma patients with a high risk of poor survival was established, highlighting the relationship between prognosis and the local immune response.