Integrating single-cell biophysical and transcriptomic features to resolve functional heterogeneity in mantle cell lymphoma

Intratumor heterogeneity impacts disease progression and therapeutic resistance but remains poorly characterized by conventional histologic, immunophenotypic, and molecular approaches. Single-cell biophysical properties distinguish functional phenotypes complementary to these approaches, providing additional insight into cellular diversity. Here, we link both buoyant mass and stiffness to gene expression to identify clinically relevant phenotypes within primary mantle cell lymphoma (MCL) cells, using MCL as a model of biological and clinical diversity in human cancer. Linked measurements reveal that buoyant mass and stiffness characterize B cell development states from naïve to plasma cell and correlate with expression of oncogenic B cell receptor signaling genes such as <i>BLK</i> and <i>CD79A</i>. In addition, changes in cell buoyant mass within primary patient specimens ex vivo correlate with sensitivity to Bruton's tyrosine kinase inhibitors in vivo in MCL and chronic lymphocytic leukemia, another B cell malignancy. These findings highlight the value of biophysical properties as biomarkers of response in pursuit of future precision therapeutic strategies.

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Publication Details

Journal
Science Advances
Published
2025-12-05
DOI
https://doi.org/10.1126/sciadv.ady2963
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
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article

Integrating single-cell biophysical and transcriptomic features to resolve functional heterogeneity in mantle cell lymphoma

Austin I. Kim, Scott R. Manalis, Robert Allyn Redd, Liam Hackett et al.
Science Advances
Lymphoma Diagnosis and Treatment
article

Integrating single-cell biophysical and transcriptomic features to resolve functional heterogeneity in mantle cell lymphoma

Austin I. Kim, Scott R. Manalis, Robert Allyn Redd, Liam Hackett, David M. Weinstock, Adam Langenbucher, Mark Alan Murakami, Martin J. Aryee, Huiyun Liu, Matthew Steven Davids, Mingzeng Zhang, Jeremy Zhang, Christine E. Ryan, Lydie Debaize, Teemu P. Miettinen, Sarah M. Duquette, Ye Zhang, J Weekes, Ioulia Vogiatzi, Emily Sumpena, Sona Baghiyan
article en

Abstract

Intratumor heterogeneity impacts disease progression and therapeutic resistance but remains poorly characterized by conventional histologic, immunophenotypic, and molecular approaches. Single-cell biophysical properties distinguish functional phenotypes complementary to these approaches, providing additional insight into cellular diversity. Here, we link both buoyant mass and stiffness to gene expression to identify clinically relevant phenotypes within primary mantle cell lymphoma (MCL) cells, using MCL as a model of biological and clinical diversity in human cancer. Linked measurements reveal that buoyant mass and stiffness characterize B cell development states from naïve to plasma cell and correlate with expression of oncogenic B cell receptor signaling genes such as <i>BLK</i> and <i>CD79A</i>. In addition, changes in cell buoyant mass within primary patient specimens ex vivo correlate with sensitivity to Bruton's tyrosine kinase inhibitors in vivo in MCL and chronic lymphocytic leukemia, another B cell malignancy. These findings highlight the value of biophysical properties as biomarkers of response in pursuit of future precision therapeutic strategies.

Science AdvancesVol. 11(49)
Broad Institute (US), Harvard University (US), Dana-Farber Cancer Institute (US), Massachusetts Institute of Technology (US)
Openalex Percentile: Top 46%
Lymphoma Diagnosis and Treatment
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