Evidence map›Paper›PMID 39424730›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Phosphoproteomic Analysis of Signaling Pathways in Lymphomas.

Björn Häupl, Anne Christine Wilke, Henning Urlaub, Thomas Oellerich

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Björn HäuplDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt, Germany.
Anne Christine WilkeDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt, Germany.
Henning UrlaubBioanalytical Mass Spectrometry, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Thomas OellerichDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt, Germany. oellerich@em.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular fate is regulated by intricate signal transduction mediated by posttranslational protein modifications like phosphorylation to transmit information. As other cancer types, lymphomas frequently show dysregulation of signaling pathways that contribute to malignant transformation and tumor progression. For example, in diffuse large B-cell lymphoma the B-cell antigen receptor was identified as an oncogenic driver mediating cellular growth and survival signals. Thus, the elucidation of these complex signaling networks is crucial to gain insight into the mechanisms underlying tumorigenesis and to identify target proteins for innovative therapeutic approaches.Here, we describe a mass spectrometry-based phosphoproteomic approach for the global analysis of intracellular signaling events and their dynamics. The workflow combines phosphopeptide enrichment and fractionation with liquid chromatography-coupled mass spectrometry for the amino acid site-specific identification and quantification of thousands of phosphorylation events. Such global signaling analyses have great potential for the elucidation of oncogenic pathomechanisms, diagnostic biomarkers, and drug targets.

Indexed as

LymphomaPhosphoproteinsProteomicsSignal TransductionCell Line, TumorChromatography, LiquidHumansMass SpectrometryPhosphopeptidesPhosphorylationProteomeTandem Mass SpectrometryPhosphopeptidesPhosphoproteinsProteomeAntigen receptorsCellular signalingLymphomaMass spectrometryPhosphoproteomics

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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.