Evidence map›Paper›PMID 39654143›Full record

ArticleJournal of integrative bioinformatics2024

TREMSUCS-TCGA - an integrated workflow for the identification of biomarkers for treatment success.

Gabor Balogh, Natasha Jorge, Célia Dupain, Maud Kamal, Nicolas Servant, Christophe Le Tourneau, Peter F Stadler, Stephan H Bernhart

Abstract read
In one paragraph

Article in Journal of integrative bioinformatics, 2024. 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

8 authors.

Gabor BaloghInterdisciplinary Center of Bioinformatics, 9180 Leipzig University , Härtelstraße 16-18, D-04107 Leipzig, Germany.ORCID https://orcid.org/0009-0000-6056-7728
Natasha JorgeInterdisciplinary Center of Bioinformatics, 9180 Leipzig University , Härtelstraße 16-18, D-04107 Leipzig, Germany.
Célia DupainDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.
Maud KamalDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.
Nicolas ServantInserm U900 Research Unit, Saint Cloud, France.
Christophe Le TourneauDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.
Peter F StadlerInterdisciplinary Center of Bioinformatics, 9180 Leipzig University , Härtelstraße 16-18, D-04107 Leipzig, Germany.
Stephan H BernhartInterdisciplinary Center of Bioinformatics, 9180 Leipzig University , Härtelstraße 16-18, D-04107 Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many publicly available databases provide disease related data, that makes it possible to link genomic data to medical and meta-data. The cancer genome atlas (TCGA), for example, compiles tens of thousand of datasets covering a wide array of cancer types. Here we introduce an interactive and highly automatized TCGA-based workflow that links and analyses epigenomic and transcriptomic data with treatment and survival data in order to identify possible biomarkers that indicate treatment success. TREMSUCS-TCGA is flexible with respect to type of cancer and treatment and provides standard methods for differential expression analysis or DMR detection. Furthermore, it makes it possible to examine several cancer types together in a pan-cancer type approach. Parallelisation and reproducibility of all steps is ensured with the workflowmanagement system Snakemake. TREMSUCS-TCGA produces a comprehensive single report file which holds all relevant results in descriptive and tabular form that can be explored in an interactive manner. As a showcase application we describe a comprehensive analysis of the available data for the combination of patients with squamous cell carcinomas of head and neck, cervix and lung treated with cisplatin, carboplatin and the combination of carboplatin and paclitaxel. The best ranked biomarker candidates are discussed in the light of the existing literature, indicating plausible causal relationships to the relevant cancer entities.

Indexed as

Biomarkers, TumorWorkflowDatabases, GeneticFemaleHumansLung NeoplasmsNeoplasmsPaclitaxelTreatment OutcomeBiomarkers, TumorPaclitaxelbiomarkerdifferential expressiondifferentially methylated regionsprecision medicineSCCTCGA

Identifiers

PMID39654143
PMCPMC11698617

What Socratic 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 Socratic graph.