Abstract

The worldwide incidence of skin cutaneous melanoma (SKCM) is increasing at a more rapid rate than other tumors. Aberrant alternative splicing (AS) is found to be common in cancer; however, how this process contributes to cancer prognosis still remains largely unknown. Mutations in RNA-binding proteins (RBPs) may trigger great changes in the splicing process. In this study, we comprehensively analyzed DNA and RNA sequencing data and clinical information of SKCM patients, together with widespread changes in splicing patterns induced by RBP mutations. We screened mRNA expression-related and prognosis-related mutations in RBPs and investigated the potential affections of RBP mutations on splicing patterns. Mutations in 853 RBPs were demonstrated to be correlated with splicing aberrations (p < 0.01). Functional enrichment analysis revealed that these alternative splicing events (ASEs) may participate in tumor progress by regulating the modification process, cell-cycle checkpoint, metabolic pathways, MAPK signaling, PI3K-Akt signaling, and other important pathways in cancer. We also constructed a prediction model based on overall survival-related AS events (OS-ASEs) affected by RBP mutations, which exhibited a good predict efficiency with the area under the curve of 0.989. Our work highlights the importance of RBP mutations in splicing alterations and provides effective biomarkers for prediction of prognosis of SKCM.

Highlights

  • Skin cutaneous melanoma (SKCM) is the deadliest type of skin cancer, comprising

  • DNA sequence data of 467 SKCM patients were downloaded from the Cancer Genome Atlas (TCGA), while alternative splicing events (ASEs) information of 103 SKCM samples was obtained from TCGA SpliceSeq data

  • Mutations in 853 RNA-binding proteins (RBPs) were found to be obviously correlated with 19748 different ASEs (Supplementary Table 2), including 1,655 alternate acceptor site events (AA) in 1,334 genes, 1,478 alternate donor site events (AD) in 1,161 genes, 3,681 alternate promoter events (AP) in 2,280 genes, 3,665 alternate terminator events (AT) in 2,206 genes, 7,802 ESs in 4,178 genes, 85 mutually exclusive exons events (ME) in 84 genes, and 1,382 retained intron events (RI) in 1,042 genes (Figures 2B,C)

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Summary

Introduction

Skin cutaneous melanoma (SKCM) is the deadliest type of skin cancer, comprising

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