Evidence map›Paper›PMID 31074385›Full record

ArticleBMC bioinformatics2019

Predicting stage-specific cancer related genes and their dynamic modules by integrating multiple datasets.

Chaima Aouiche, Bolin Chen, Xuequn Shang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Unveiling the Bioactive Efficacy ofPharmaceuticals (Basel, Switzerland) · 2024
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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

3 authors.

Chaima AouicheSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China.
Bolin ChenSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China. blchen@nwpu.edu.cn.
Xuequn ShangSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mechanism of many complex diseases has not been detected accurately in terms of their stage evolution. Previous studies mainly focus on the identification of associations between genes and individual diseases, but less is known about their associations with specific disease stages. Exploring biological modules through different disease stages could provide valuable knowledge to genomic and clinical research.

resultsIn this study, we proposed a powerful and versatile framework to identify stage-specific cancer related genes and their dynamic modules by integrating multiple datasets. The discovered modules and their specific-signature genes were significantly enriched in many relevant known pathways. To further illustrate the dynamic evolution of these clinical-stages, a pathway network was built by taking individual pathways as vertices and the overlapping relationship between their annotated genes as edges.

conclusionsThe identified pathway network not only help us to understand the functional evolution of complex diseases, but also useful for clinical management to select the optimum treatment regimens and the appropriate drugs for patients.

Indexed as

AlgorithmsGene Regulatory NetworksComputational BiologyDatabases, GeneticDisease ProgressionHumansMolecular Sequence AnnotationNeoplasm ProteinsNeoplasmsNeoplasm StagingPredictive Value of TestsNeoplasm ProteinsClinical stagesDisease evolutionDisease genesDynamic modulesPathway networks

Identifiers

PMID31074385
PMCPMC6509867

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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.