Evidence map›Paper›PMID 34430408›Full record

ArticleTranslational andrology and urology2021

Comprehensive analysis of alternative splicing profiling reveals novel events associated with prognosis and the infiltration of immune cells in prostate cancer.

Tianqi Wu, Wenfeng Wang, Yanhao Wang, Mengfei Yao, Leilei Du, Xingming Zhang, Yongqiang Huang, Jianhua Wang, Hongbo Yu, Xiaojie Bian

Open access · diamondAbstract read
In one paragraph

Article in Translational andrology and urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Tianqi WuShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Wenfeng WangShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Yanhao WangShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Mengfei YaoShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Leilei DuShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Xingming ZhangShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Yongqiang HuangShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Jianhua WangShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Hongbo YuDepartment of Urology, Affiliated Mingji Hospital of Nanjing Medical University, Nanjing, China.
Xiaojie BianShanghai Urological Cancer Institute, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Fudan University Shanghai Cancer Center · CNAnhui University of Science and Technology · CNNanjing Medical University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlternative splicing (AS) is believed to play a vital role in tumor development. Therefore, comprehensive investigation of AS and its biological function in prostate cancer (PCa) is crucial.

methodsThe AS profiling of 489 patients with PCa was obtained from The Cancer Genome Atlas (TCGA) SpliceSeq database. Bioinformatics tools were used to describe splicing associations and build prognostic models. Unsupervised clustering of the determined prognostic AS events and the relationship with immune characteristics were also explored.

resultsIn total, 20,723 AS events were detected and 2,805 were identified in PCa. In the regulatory networks, the data suggested a significant correlation between splicing factor (SF) expression and AS events. To stratify the progression risk of PCa patients, prognostic models were constructed using splicing patterns. Six AS events were screened out as independent prognostic factors for progression-free survival. Based on the gene features, we constructed the combined prognostic predictors model, and the receiver operating characteristic (ROC) curve for this model reached a high area under the ROC curve (AUC) of 0.729793, indicating a favorable ability to predict patient outcomes. Through unsupervised clustering analysis, the correlations between AS-based clusters and prognosis as well as immune characteristics were revealed. The correlation analysis on TIMER revealed the relationship between gene expression and immune cell infiltration.

conclusionsThis in-depth genome-wide analysis of the AS profiling in PCa revealed unique AS events associated with cancer progression and the infiltration of immune cells, with potential for predicting outcomes and therapeutic responses.

Indexed as

Alternative splicing (AS)immune cells infiltrationprognosisprostate cancer (PCa)

Identifiers

PMID34430408
PMCPMC8350246
OpenAlexW3186490731

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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.