Evidence map›Paper›PMID 42878760›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Pathway and Kinase Analysis in Proteomics and Phosphoproteomics with rROMA.

Stéphane Liva, Anne-Claire Kröger, Michael Richard, Patrick Poullet, Loredana Martignetti

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Article in Methods in molecular biology (Clifton, N.J.), 2027. 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
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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.

Stéphane LivaInstitut Curie, PSL University, Paris, France.
Anne-Claire KrögerInstitut Curie, PSL University, Paris, France.
Michael RichardInstitut Curie, PSL University, Paris, France.
Patrick PoulletInstitut Curie, PSL University, Paris, France.
Loredana MartignettiInstitut Curie, PSL University, Paris, France. Loredana.Martignetti@curie.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in data acquisition tools, particularly mass spectrometry-based techniques, have made high-throughput methods like proteomics and phosphoproteomics increasingly accessible. However, the volume and complexity of the data require specialized computational tools for analysis and interpretation to extract meaningful insights. Here, we describe the use of rROMA software to analyze pathway and kinase activity in proteomic and phosphoproteomic datasets. rROMA is an open-source package available on Github at: www.github.com/sysbio-curie/rROMA . As a case study, we applied rROMA to breast cancer samples from the Clinical Proteomic Tumor Analysis Consortium (CPTAC), which provides precise relative quantification of proteins and phosphorylation sites of a large cohort of breast cancer samples through Tandem mass tag (TMT)-based mass spectrometry. These analyses illustrate how to identify active pathways and kinase-driven mechanisms potentially involved in disease subtypes, along with their associated proteins and phosphosites.

Indexed as

Computational BiologyPhosphoproteinsPhosphotransferasesProtein KinasesProteomicsSoftwareBreast NeoplasmsFemaleHumansPhosphorylationSignal TransductionTandem Mass SpectrometryPhosphoproteinsPhosphotransferasesProtein KinasesKinase activityPathway analysisPhosphoproteomicsProteomics

Identifiers

PMID42878760

What OpenQuestion holds

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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.