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Updated: Nov 5, 2025

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
Published on: April 26, 2017
Splicing factor SRSF1 promotes breast cancer progression via oncogenic splice switching of PTPMT1
Jun-Xian Du1, Yi-Hong Luo1, Si-Jia Zhang1
1Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Background:
Intensive 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.
Methods:
We 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.
Results:
SRSF1 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.
Conclusions:
SRSF1 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.
Insights
SRSF1 promotes breast cancer (BRCA) by regulating alternative splicing (AS) of PTPMT1, impacting proliferation and migration. This splicing event offers a potential therapeutic target and prognostic marker for BRCA patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Aberrant alternative splicing (AS) driven by SR protein family dysregulation impacts cancer progression.
- The specific role of SRSF1 in breast cancer (BRCA) and its associated AS events remain unclear.
Purpose of the Study:
- To investigate the molecular function of SRSF1 in BRCA.
- To identify key AS events regulated by SRSF1 in BRCA progression.
Main Methods:
- Comprehensive analysis of SRSF1 expression and clinical correlation using TCGA, Metabric, and clinical samples.
- In vitro and in vivo functional assays to assess SRSF1's role in BRCA.
- RNA-seq, RIP-PCR, and CLIP to identify SRSF1-mediated AS events and binding motifs.
- Minigene reporter assays for validation.
- Analysis of PTPMT1 exon 3 (E3) AS and its mediation of SRSF1's oncogenic role via the AKT/C-MYC axis.
Main Results:
- SRSF1 is upregulated in BRCA, correlating with higher tumor grade, Ki-67 index, and poorer prognosis in HR+ patients.
- SRSF1 promotes proliferation, migration, and inhibits apoptosis in BRCA cells.
- SRSF1 directly binds to a motif in PTPMT1 exon 3, regulating its alternative splicing.
- PTPMT1 splice switching partially mediates SRSF1's oncogenic function through the AKT/C-MYC pathway.
- PTPMT1 AS and SRSF1 expression identify a high-risk group with poorer prognosis in early-stage BRCA.
Conclusions:
- SRSF1 plays an oncogenic role in BRCA by regulating PTPMT1 alternative splicing.
- PTPMT1 AS is a potential therapeutic target and prognostic factor in HR+ BRCA.
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