Evidence map›Paper›PMID 36731897›Full record

ArticleJournal of gynecologic oncology2023

Alternative splicing of

Sisi He, Rong Cao, Yan Mao, Na Li, Yanzhe Wang, Hu Ma, Kunming Tian

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
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

7 authors at 2 institutions in 1 country.

Sisi He *Department of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0002-1492-0532
Rong Cao *The Second Clinical College, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0001-9379-3297
Yan MaoDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0001-5822-1859
Na LiDepartment of Gynecology and Obstetrics, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0002-3681-8168
Yanzhe WangDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0002-8955-7483
Hu MaDepartment of Oncology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0003-3146-293X
Kunming TianDepartment of Gynecology and Obstetrics, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China.ORCID 0000-0002-0570-9540
Zunyi Medical University · CNHuazhong University of Science and Technology · CN

Funding

Natural Science Foundation of Guangzhou City (2022)626Zunyi City Science and Technology Plan Project (2022)402Zunyi Medical University 2018 F-913
6 · The paper itself

Abstract

objectiveAccumulating evidence has shown that aberrant alternative splicing events are closely associated with the onset and development of cancer. However, whether genetic variants-associated alternative splicing is linked to risk of endometrial cancer remains largely uncertain.

methodsWe identified single nucleotide polymorphisms (SNPs) locates in the splicing number trait locus (sQTL) of endometrial cancer using the CancerSplicing QTL database. In parallel with bioinformatics analysis, we conducted a case-control study comprising 2,000 cases and 2,013 controls to assess the association between identified SNP which possesses mRNA splicing function and endometrial cancer susceptibility. Furthermore, we used the Kaplan-Meier Plotter, The Human Protein Atlas, SPNR, and Spliceman2 databases for sQTL and differential gene expression analyses to identify the genetic variant which most potentially influence the risk of endometrial cancer through alternative splicing to reveal the potential mechanism by which candidate SNPs regulate the risk of endometrial cancer.

resultsThe results indicated that SNP rs7128029 A<G was significantly associated with an increased risk of endometrial cancer (odds ratio=1.384; 95% confidence interval=1.038-1.964). Moreover, the carcinogenic effect of SNP rs7128029 A<G was consistently revealed by propensity matching analysis, an additive model, and a dominant model. Importantly, sQTL analysis showed that SNP rs7128029 could affect the transcriptional modification of

conclusionThese findings suggest that SNP rs7128029-mediated alternative splicing events in

Indexed as

Alternative SplicingEndometrial NeoplasmsCase-Control StudiesDatabases, FactualFemaleHumansOdds RatioPolymorphism, Single NucleotideProteasome Endopeptidase ComplexRisk26S proteasome non-ATPase regulatory subunit 13Proteasome Endopeptidase Complex26S Proteasome Non-ATPase Regulatory Subunit 13Alternative SplicingEndometrial CancerSingle Nucleotide Polymorphism

Identifiers

PMID36731897
PMCPMC10157344
OpenAlexW4319058106

What OpenQuestion holds

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Registered trials

None linked

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.