Evidence map›Paper›PMID 33992102›Full record

ArticleJournal of experimental & clinical cancer research : CR2021

Splicing factor SRSF1 promotes breast cancer progression via oncogenic splice switching of PTPMT1.

Jun-Xian Du, Yi-Hong Luo, Si-Jia Zhang, Biao Wang, Cong Chen, Gui-Qi Zhu, Ping Zhu, Cheng-Zhe Cai, Jing-Lei Wan, Jia-Liang Cai and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 114 citations in OpenAlex.

  1. SRSF3 plays a key role in liver cancer sex disparity by facilitating hepatocyte expression of ERα and FOXA.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. The cellular landscape of druggable RNA-binding proteins.Nature reviews. Drug discovery · 2026
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10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Jun-Xian Du *Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Yi-Hong Luo *Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Si-Jia Zhang *Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Biao Wang *Liver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China.
Cong ChenDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Gui-Qi ZhuLiver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China.
Ping ZhuDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Fudan University, No. 130 Dongan Road, Shanghai, 200032, China.
Cheng-Zhe CaiDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Jing-Lei WanLiver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China.
Jia-Liang CaiLiver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China.
Shi-Ping ChenLiver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China.
Zhi DaiLiver Cancer Institute, Zhongshan Hospital, Fudan University & State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, 200032, China. dai.zhi@zs-hospital.sh.cn.
Wei ZhuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. drzhu@163.com.
Zhongshan Hospital · CNFudan University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CN

Funding

Excellent Backbone Plan of Zhongshan Hospital in 2019 2019ZSGG08National Natural Science Fund of China 81871916; 82072670; 81672330National Natural Science Fund of China 82072908
6 · The paper itself

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.

Indexed as

Alternative SplicingBreast NeoplasmsDisease ProgressionFemaleHumansOncogenesProtein Tyrosine PhosphatasesPTEN PhosphohydrolaseSerine-Arginine Splicing FactorsProtein Tyrosine PhosphatasesPTEN PhosphohydrolasePtpmt1 protein, humanSerine-Arginine Splicing FactorsSRSF1 protein, humanAlternative splicingBreast cancerP-AKT-C-MYCPTPMT1SRSF1

Identifiers

PMID33992102
PMCPMC8122567
OpenAlexW3161397791

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.