Abstract
BackgroundIntensive evidence has highlighted the effect of aberrant alternative splicing (AS) events on cancer progression when triggered by dysregulation of the SR protein family. Nonetheless, the underlying mechanism in breast cancer (BRCA) remains elusive. Here we sought to explore the molecular function of SRSF1 and identify the key AS events regulated by SRSF1 in BRCA.MethodsWe conducted a comprehensive analysis of the expression and clinical correlation of SRSF1 in BRCA based on the TCGA dataset, Metabric database and clinical tissue samples. Functional analysis of SRSF1 in BRCA was conducted in vitro and in vivo. SRSF1-mediated AS events and their binding motifs were identified by RNA-seq, RNA immunoprecipitation-PCR (RIP-PCR) and in vivo crosslinking followed by immunoprecipitation (CLIP), which was further validated by the minigene reporter assay. PTPMT1 exon 3 (E3) AS was identified to partially mediate the oncogenic role of SRSF1 by the P-AKT/C-MYC axis. Finally, the expression and clinical significance of these AS events were validated in clinical samples and using the TCGA database.ResultsSRSF1 expression was consistently upregulated in BRCA samples, positively associated with tumor grade and the Ki-67 index, and correlated with poor prognosis in a hormone receptor-positive (HR+) cohort, which facilitated proliferation, cell migration and inhibited apoptosis in vitro and in vivo. We identified SRSF1-mediated AS events and discovered the SRSF1 binding motif in the regulation of splice switching of PTPMT1. Furthermore, PTPMT1 splice switching was regulated by SRSF1 by binding directly to its motif in E3 which partially mediated the oncogenic role of SRSF1 by the AKT/C-MYC axis. Additionally, PTPMT1 splice switching was validated in tissue samples of BRCA patients and using the TCGA database. The high-risk group, identified by AS of PTPMT1 and expression of SRSF1, possessed poorer prognosis in the stage I/II TCGA BRCA cohort.ConclusionsSRSF1 exerts oncogenic roles in BRCA partially by regulating the AS of PTPMT1, which could be a therapeutic target candidate in BRCA and a prognostic factor in HR+ BRCA patient.
Highlights
Intensive evidence has highlighted the effect of aberrant alternative splicing (AS) events on cancer progression when triggered by dysregulation of the SR protein family
SRSF1 is increased in breast cancer (BRCA), and its high expression predicts poor prognosis in HR+ BRCA patients To explore the expression alteration of SR family proteins in BRCA, we analyzed the differentially expressed SR proteins in the samples from the TCGA dataset (Fig. 1a)
KaplanMeier analysis showed that patients with higher expression levels of SRSF1 had poorer overall survival (OS) in the HR+ cohort (P = 0.0114) (Fig. 1e), while there was no significant difference in the OS of the HR- cohort (P = 0.1452) (Fig. 1f)
Summary
Intensive evidence has highlighted the effect of aberrant alternative splicing (AS) events on cancer progression when triggered by dysregulation of the SR protein family. We sought to explore the molecular function of SRSF1 and identify the key AS events regulated by SRSF1 in BRCA. Statistics in 2019 showed that among all age groups, HR+ BRCA is the most prevalent molecular subtype [2]. As a widespread and pivotal posttranscriptional regulation method, aberrant AS events are involved in the pathogenesis of various diseases, including cancer. Switching of splice isoforms caused by abnormal AS is widely involved in the regulation of cancer phenotypes, including proliferation, apoptosis, cell cycle progression, invasion and metastasis, angiogenesis, abnormal energy metabolism and immune escape [5]. In BRCA, multiple genes such as BRAC1, FGFR1/2, HER2, and DMTF1/KLF6 have been reported to undergo abnormal AS, resulting in isoforms with different or even opposite functions [6]
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