Evidence map›Paper›PMID 33020551›Full record

ArticleScientific reports2020

Transcriptome-wide analysis and modelling of prognostic alternative splicing signatures in invasive breast cancer: a prospective clinical study.

Linbang Wang, Yuanyuan Wang, Bao Su, Ping Yu, Junfeng He, Lei Meng, Qi Xiao, Jinhui Sun, Kai Zhou, Yuzhou Xue and 1 more

Open access · goldAbstract readClinical Study
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Investigation into theFrontiers in pharmacology · 2022
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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

11 authors at 2 institutions in 1 country.

Linbang Wang *Department of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Yuanyuan Wang *Department of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Bao SuDepartment of Orthopedic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Ping YuDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Junfeng HeDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Lei MengDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Qi XiaoDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Jinhui SunDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Kai ZhouDepartment of Orthopedic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Yuzhou XueDepartment of Orthopedic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Jinxiang TanDepartment of Endocrine and Breast Surgery, The First Affliated Hospital of Chongqing Medical University, Chongqing, 400016, China. tjx1202@163.com.
First Affiliated Hospital of Chongqing Medical University · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant alternative splicing (AS) has been highly involved in the tumorigenesis and progression of most cancers. The potential role of AS in invasive breast cancer (IBC) remains largely unknown. In this study, RNA sequencing of IBC samples from The Cancer Genome Atlas was acquired. AS events were screened by conducting univariate and multivariate Cox analysis and least absolute shrinkage and selection operator regression. In total, 2146 survival-related AS events were identified from 1551 parental genes, of which 93 were related to prognosis, and a prognostic marker model containing 14 AS events was constructed. We also constructed the regulatory network of splicing factors (SFs) and AS events, and identified DDX39B as the node SF gene, and verified the accuracy of the network through experiments. Next, we performed quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) in triple negative breast cancer patients with different responses to neoadjuvant chemotherapy, and found that the exon-specific expression of EPHX2, C6orf141, and HERC4 was associated with the different status of patients that received neoadjuvant chemotherapy. In conclusion, this study found that DDX39B, EPHX2 (exo7), and HERC4 (exo23) can be used as potential targets for the treatment of breast cancer, which provides a new idea for the treatment of breast cancer.

Indexed as

Alternative SplicingBiomarkers, TumorBreast NeoplasmsChinaDEAD-box RNA HelicasesEpoxide HydrolasesFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansKaplan-Meier EstimatePrognosisRNA, MessengerRNA Splicing FactorsSequence Analysis, RNABiomarkers, TumorDDX39B protein, humanDEAD-box RNA HelicasesEPHX2 protein, humanEpoxide HydrolasesHERC4 protein, humanRNA, MessengerRNA Splicing FactorsUbiquitin-Protein Ligases

Identifiers

PMID33020551
PMCPMC7536242
OpenAlexW3089579190

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.