Abstract

BackgroundBreast cancer (BRCA) is one of the most common cancers worldwide. Abnormal alternative splicing (AS) frequently observed in cancers. This study aims to demonstrate AS events and signatures that might serve as prognostic indicators for BRCA.MethodsOriginal data for all seven types of splice events were obtained from TCGA SpliceSeq database. RNA-seq and clinical data of BRCA cohorts were downloaded from TCGA database. Survival-associated AS events in BRCA were analyzed by univariate COX proportional hazards regression model. Prognostic signatures were constructed for prognosis prediction in patients with BRCA based on survival-associated AS events. Pearson correlation analysis was performed to measure the correlation between the expression of splicing factors (SFs) and the percent spliced in (PSI) values of AS events. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were conducted to demonstrate pathways in which survival-associated AS event is enriched.ResultsA total of 45,421 AS events in 21,232 genes were identified. Among them, 1121 AS events in 931 genes significantly correlated with survival for BRCA. The established AS prognostic signatures of seven types could accurately predict BRCA prognosis. The comprehensive AS signature could serve as independent prognostic factor for BRCA. A SF-AS regulatory network was therefore established based on the correlation between the expression levels of SFs and PSI values of AS events.ConclusionsThis study revealed survival-associated AS events and signatures that may help predict the survival outcomes of patients with BRCA. Additionally, the constructed SF-AS networks in BRCA can reveal the underlying regulatory mechanisms in BRCA.

Highlights

  • Breast cancer (BRCA) is one of the most common cancers worldwide

  • 3731 alternate acceptor site (AA) events in 2628 genes, 3246 alternate donor site (AD) events in 2278 genes, 9112 alternate promoter (AP) events in 3654 genes, 8595 alternate terminator (AT) events in 3755 genes, 17,702 exon skip (ES) events in 6812 genes, 233 mutually exclusive exon (ME) events in 227 genes, and 2802 retained intron (RI) events in 1878 genes were observed in preliminary analysis (Fig. 1a)

  • 88 AA events in 85 genes, 83 AD events in 82 genes, 281 AP events in 190 genes, 62 AT events in 42 genes, 526 ES events in 453 genes, 8 ME events in 7 genes, and 74 RI events in 71 genes were identified as prognostic alternative splicing (AS) events (Fig. 1c)

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Summary

Introduction

Breast cancer (BRCA) is one of the most common cancers worldwide. Abnormal alternative splicing (AS) frequently observed in cancers. This study aims to demonstrate AS events and signatures that might serve as prognostic indicators for BRCA. BRCA ranks among the top most common female malignancies in China and worldwide [1, 2]. In the Alternative splicing (AS) is an important posttranscriptional process through which multiple transcripts. There are seven types of AS events including exon skip (ES), alternate donor site (AD), alternate acceptor site (AA), mutually exclusive exon (ME), alternate terminator (AT), alternate promoter (AP), and retained intron (RI). AS events were reported to serve as prognostic predictors for multiple types of cancer [12]

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