Proteome landscape of B-cell malignancies identifies mantle cell lymphoma protein signature

Mantle cell lymphoma (MCL) is one of the deadliest forms of Non-Hodgkins B-cell lymphoma. Typically, patients present with both overexpression of CyclinD1 and secondary mutations identified by genomic sequencing. Although MCL patients may initially respond to treatment, they eventually relapse and succumb to disease, highlighting the essential need to identify new targets for treatment. Here we performed proteomic profiling of healthy B cells and three different forms of B-cell malignancies, including MCL, to define the proteomic signature of MCL. We compared the proteome of each to MCL and identified 10 proteins that are specifically upregulated in MCL. Of these 10 proteins, seven of them show no transcriptional changes and have been overlooked by conventional RNA expression analysis. Further analysis of the proteomic signature reveals potential avenues for dual targeting in CAR T-cell therapy and provides guidance for personalized therapeutics based on protein expression.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-05
DOI
https://doi.org/10.64898/2026.03.02.709116
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Proteome landscape of B-cell malignancies identifies mantle cell lymphoma protein signature

Timothy C. Greiner, Karli J. Wittorf, Samantha Swenson, Kasidy K. Dobish et al.
bioRxiv (Cold Spring Harbor Laboratory)
Lymphoma Diagnosis and Treatment
article

Proteome landscape of B-cell malignancies identifies mantle cell lymphoma protein signature

Timothy C. Greiner, Karli J. Wittorf, Samantha Swenson, Kasidy K. Dobish, Nicholas T R Woods, Shannon M Buckley, Michael R Green, Julie M Vose, C Bea Winship, Henry CH Law
article en

Abstract

Mantle cell lymphoma (MCL) is one of the deadliest forms of Non-Hodgkins B-cell lymphoma. Typically, patients present with both overexpression of CyclinD1 and secondary mutations identified by genomic sequencing. Although MCL patients may initially respond to treatment, they eventually relapse and succumb to disease, highlighting the essential need to identify new targets for treatment. Here we performed proteomic profiling of healthy B cells and three different forms of B-cell malignancies, including MCL, to define the proteomic signature of MCL. We compared the proteome of each to MCL and identified 10 proteins that are specifically upregulated in MCL. Of these 10 proteins, seven of them show no transcriptional changes and have been overlooked by conventional RNA expression analysis. Further analysis of the proteomic signature reveals potential avenues for dual targeting in CAR T-cell therapy and provides guidance for personalized therapeutics based on protein expression.

bioRxiv (Cold Spring Harbor Laboratory)
Creighton University (US), The University of Texas MD Anderson Cancer Center (US), University of Utah (US), Huntsman Cancer Institute (US), University of Nebraska Medical Center (US)
Good health and well-being
Openalex Percentile: Top 34%
Lymphoma Diagnosis and Treatment
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