Evidence map›Paper›PMID 41024516›Full record

ArticleCell cycle (Georgetown, Tex.)

Identification of progression markers for prostate cancer.

Jie Song, Yang Zhou, Harald Hedman, Tommi Rantapero, Maréne Landström

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Jie SongDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.ORCID 0000-0002-4955-9118
Yang ZhouDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Harald HedmanDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Tommi RantaperoGenevia Technologies, Tampere, Finland.
Maréne LandströmDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.ORCID 0000-0001-6737-7230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TGFβ functions as a tumor suppressor or promoter, depending on the context, making TGFβ a useful predictive biomarker. Genes related to TGFβ signaling and Aurora kinase were tested for their ability to predict the progression risk of primary prostate tumors. Using data from The Cancer Genome Atlas (TCGA), we trained an elastic-net regularized Cox regression model including a minimal set of gene expression, copy number (CN), and clinical data. A multi-step feature selection and regularization scheme was applied to minimize the number of features while maintaining predictive power. An independent hold-out cohort was used to validate the model. Expanding from prostate cancer, predictive models were similarly trained on all other eligible cancer types in TCGA.

Indexed as

Biomarkers, TumorProstatic NeoplasmsAurora Kinase AAurora Kinase BDisease ProgressionGene Expression Regulation, NeoplasticHumansKinesinsMaleProportional Hazards ModelsSignal TransductionTransforming Growth Factor betaAURKA protein, humanAURKB protein, humanAurora Kinase AAurora Kinase BBiomarkers, TumorKinesinsTransforming Growth Factor betaAURKA/BCancerKIF23prognostic modelingTGFBR1

Identifiers

PMID41024516
PMCPMC12533958

What OpenQuestion holds

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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.