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.

Abstract

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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