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SRSF3-Regulated RNA Alternative Splicing Promotes Glioblastoma Tumorigenicity by Affecting Multiple Cellular Processes.

Authors :
Song X
Wan X
Huang T
Zeng C
Sastry N
Wu B
James CD
Horbinski C
Nakano I
Zhang W
Hu B
Cheng SY
Source :
Cancer research [Cancer Res] 2019 Oct 15; Vol. 79 (20), pp. 5288-5301. Date of Electronic Publication: 2019 Aug 28.
Publication Year :
2019

Abstract

Misregulated alternative RNA splicing (AS) contributes to the tumorigenesis and progression of human cancers, including glioblastoma (GBM). Here, we showed that a major splicing factor, serine and arginine rich splicing factor 3 (SRSF3), was frequently upregulated in clinical glioma specimens and that elevated SRSF3 was associated with tumor progression and a poor prognosis for patients with glioma. In patient-derived glioma stem-like cells (GSC), SRSF3 expression promoted cell proliferation, self-renewal, and tumorigenesis. Transcriptomic profiling identified more than 1,000 SRSF3-affected AS events, with a preference for exon skipping in genes involved with cell mitosis. Motif analysis identified the sequence of CA(G/C/A)CC(C/A) as a potential exonic splicing enhancer for these SRSF3-regulated exons. To evaluate the biological impact of SRSF3-affected AS events, four candidates were selected whose AS correlated with SRSF3 expression in glioma tissues, and their splicing pattern was modified using a CRISPR/Cas9 approach. Two functionally validated AS candidates were further investigated for the mechanisms underlying their isoform-specific functions. Specifically, following knockout of SRSF3, transcription factor ETS variant 1 ( ETV1 ) gene showed exon skipping at exon 7, while nudE neurodevelopment protein 1 ( NDE1 ) gene showed replacement of terminal exon 9 with a mutually exclusive exon 9'. SRSF3-regulated AS of these two genes markedly increased their oncogenic activity in GSCs. Taken together, our data demonstrate that SRSF3 is a key regulator of AS in GBM and that understanding mechanisms of misregulated AS could provide critical insights for developing effective therapeutic strategies against GBMs. SIGNIFICANCE: SRSF3 is a significant regulator of glioma-associated alternative splicing, implicating SRSF3 as an oncogenic factor that contributes to the tumor biology of GBM.<br /> (©2019 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1538-7445
Volume :
79
Issue :
20
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
31462429
Full Text :
https://doi.org/10.1158/0008-5472.CAN-19-1504