Evidence map›Paper›PMID 41096573›Full record

ArticleInternational journal of molecular sciences2025

Proteomic Profiling of Limited-Stage Follicular Lymphoma Reveals Differentially Expressed Proteins Linked to Disease Progression Post-Radiation Therapy.

Jonas Klejs Hemmingsen, Marie Hairing Enemark, Emma Frasez Sørensen, Cecilie Dohrmann, Kristina Lystlund Lauridsen, Stephen Jacques Hamilton-Dutoit, Robert Kridel, Bent Honoré, Maja Ludvigsen

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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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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

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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

9 authors.

Jonas Klejs HemmingsenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0009-0007-5706-3407
Marie Hairing EnemarkDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0003-4086-5183
Emma Frasez SørensenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0009-0003-4588-5607
Cecilie DohrmannDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0009-0001-4076-6516
Kristina Lystlund LauridsenDepartment of Pathology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Stephen Jacques Hamilton-DutoitDepartment of Pathology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0003-2158-3885
Robert KridelPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.ORCID 0000-0003-0287-7124
Bent HonoréDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.ORCID 0000-0002-3459-7429
Maja LudvigsenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0001-5089-3271

Funding

Aarhus University xxxA. P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal xxxKaren Elise Jensen Foundation xxx
6 · The paper itself

Abstract

Follicular lymphoma (FL) is the most common indolent lymphoma. Despite a generally favorable prognosis and long-term survival for many patients, FL remains incurable, with disease progression occurring in approximately half of limited-stage FL cases. In this study, we employed high-throughput mass spectrometry-based proteomics to explore the differential protein expression in diagnostic lymphoma biopsies from 26 limited-stage FL patients. Of these, 9 patients experienced subsequent disease progression (sp-FL), while 17 did not (np-FL). A total of 1940 proteins were identified, with 78 showing significant differential expression between progressing and non-progressing cases. Unsupervised clustering analyses were able to separate the two patient groups based on these differential protein profiles. Notably, proteins involved in metabolism, immune regulation, and apoptosis were downregulated in sp-FL samples. Among the identified proteins, caspase 4 and 8 (CASP4 and CASP8) were further evaluated. The low expression of CASP4 in the diagnostic lymphoma tissue correlated with shorter progression-free survival (PFS) (

Indexed as

Lymphoma, FollicularProteomeProteomicsAdultAgedBiomarkers, TumorCaspase 8Disease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisBiomarkers, TumorCaspase 8Proteomedisease progressionfollicular lymphomanon-Hodgkin lymphomaproteomicsradiation therapy

Identifiers

PMID41096573
PMCPMC12525013

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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.