Evidence map›Paper›PMID 40464949›Full record

ArticleCellular and molecular life sciences : CMLS2025

CD151 interacts with integrin beta 2 in B cell lymphomas.

Philipp M Hagemann, Angelique N Kenyon, Alfredo Cabrera-Orefice, Abbey B Arp, Eva A M Hesius, Michiel van den Brand, Sjoerd J van Deventer, Daphne de Jong, Blanca Scheijen, Zijun Y Xu-Monette and 6 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. 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

16 authors.

Philipp M HagemannDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-2139-9471
Angelique N KenyonDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0009-0005-9295-1923
Alfredo Cabrera-OreficeRadboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-2042-3794
Abbey B ArpDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0009-0003-6727-3273
Eva A M HesiusDepartment of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0009-0000-0319-7505
Michiel van den BrandPathology-DNA, Rijnstate Hospital, Arnhem, The Netherlands.ORCID http://orcid.org/0000-0001-8871-6254
Sjoerd J van DeventerDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0001-8972-6665
Daphne de JongDepartment of Pathology, Antoni Van Leeuwenhoek Hospital/The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-9725-4060
Blanca ScheijenDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0001-8029-9230
Zijun Y Xu-MonetteHematopathology Division and Department of Pathology, Duke University Medical Center, Durham, NC, USA.ORCID http://orcid.org/0000-0002-7615-3949
Ulrich BrandtRadboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-1869-6811
Cornelia G SpruijtDepartment of Molecular Biology, Faculty of Science, Oncode Institute, Radboud University Nijmegen, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-1789-670X
Michiel VermeulenDepartment of Molecular Biology, Faculty of Science, Oncode Institute, Radboud University Nijmegen, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-0836-6894
Martin Ter BeestDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.
Ken H YoungHematopathology Division and Department of Pathology, Duke University Medical Center, Durham, NC, USA.ORCID http://orcid.org/0000-0002-5755-8932
Annemiek B van SprielDepartment of Medical BioSciences, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands. annemiek.vanspriel@radboudumc.nl.ORCID http://orcid.org/0000-0002-3590-2368

Funding

European Research Council 101112687H2020 European Research Council 724281KWF Kankerbestrijding 12949KWF Kankerbestrijding 14726Nederlandse Organisatie voor Wetenschappelijk Onderzoek Gravitation programme IMAGINE! (project number 24.005.009Nederlandse Organisatie voor Wetenschappelijk Onderzoek the Institute of Chemical Immunology (project ICI 000-23)ZonMw 09120012010023
6 · The paper itself

Abstract

CD151 is a broadly expressed four-transmembrane protein (tetraspanin) that interacts with laminin-binding integrins like integrin alpha 3 (ITGA3). CD151 drives tumor development and expression correlates with poor prognosis in solid cancers, but CD151 has not been studied in B cell malignancies. We investigated CD151 expression on normal human B cells and B cell lymphomas using highly sensitive flow cytometry and immunohistochemistry. Expression of CD151 increased during B cell differentiation from naïve to memory B cells to plasma cells. B lymphoma cell lines and human lymphoma biopsy samples expressed higher levels of CD151 compared to normal B cells, but CD151-deficient lymphomas were identified as well. To investigate the function of CD151 in B cells, CD151-deficient and stably transduced CD151 expressing B lymphoma cell lines were generated. Immunoprecipitation-mass spectrometry analysis of CD151 protein complexes identified integrin beta 2 (ITGB2) as new interaction partner in lymphoma cells. Deficiency of CD151 decreased cell surface expression of alpha integrin subunits L (ITGAL) and M (ITGAM), and impaired ICAM-1-mediated cell spreading. Interestingly, B cells and lymphomas did not express ITGA3-bound CD151 compared to T cells that expressed two different populations of integrin-bound and integrin-free CD151. Despite CD151 expression not being related to clinical outcome of patients with diffuse large B cell lymphoma (DLBCL), CD151 expression was predominantly detected in the activated (ABC) subset of DLBCL. Taken together, we identified a new molecular association of CD151 with ITGB2, and targeting integrin-free CD151 in DLBCL may represent a new target for immunotherapy.

Indexed as

Lymphoma, B-CellTetraspanin 24B-LymphocytesCell Line, TumorHumansIntegrin alpha3Protein BindingCD151 protein, humanIntegrin alpha3Tetraspanin 24CD18Cell spreadingMembrane proteinNon-Hodgkin lymphomaTSPAN24

Identifiers

PMID40464949
PMCPMC12137850

What OpenQuestion 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 OpenQuestion graph.