bioRxiv Science⌕ Search

Biology subjects

Chung, E. K.

Publications and source records attributed to Chung, E. K..

2 recordsLinked to original sources

Spatialproteomics - an interoperable toolbox for analyzing highly multiplexed fluorescence image data

SummaryHighly multiplexed immunofluorescence imaging is a recent method to characterize tissues at single-cell resolution on the protein level, offering low cost, high scalability, and the ability to analyze paraffin-embedded tissue samples. However, the analysis of these data involves a sequence of steps, including segmentation, image processing, marker quantification, cell type classification, and neighborhood analysis, each of which involves a multitude of method and parameter choices that need to be adapted to the data and analytical objective at hand. Moreover, variations in data quality can be high and unpredictable, which necessitates further flexibility and interactivity. While individual components exist, there is an unmet need for a coherent toolbox that offers end-to-end coverage of the workflow, flexibility, and automation. We present spatialproteomics, a Python package that addresses these challenges. Built on top of xarray and dask, spatialproteomics can process images that are larger than the working memory. It supports synchronization of shared coordinates across data modalities such as images, segmentation masks, and expression matrices, which facilitates easy and safe subsetting and transformation. We demonstrate spatialproteomics on a set of images of reactive lymph nodes or different forms of B cell Non-Hodgkin lymphomas (BNHL) from 132 patients. We showcase an end-to-end analysis from raw images to statistical characterization of cell type composition and spatial distribution across indolent and aggressive lymphomas. Furthermore, we show how spatialproteomics can process gigapixel whole slide images. Altogether, we propose spatialproteomics as an easy-to-install, easy-to-learn, comprehensive toolbox for constructing powerful end-to-end image analysis solutions for highly multiplexed immunofluorescence imaging. Availability and ImplementationThe source code for spatialproteomics is freely available at https://github.com/sagar87/spatialproteomics under the MIT license. Contactwolfgang.huber@embl.org, Peter-Martin.Bruch@med.uni-duesseldorf.de

bioinformatics↗

A single-cell multi-omic and spatial atlas of nodal B-cell lymphomas reveals B-cell maturation drives intratumor heterogeneity

Intratumor heterogeneity underpins cancer pathogenesis and evolution, although it is typically considered independent from the differentiation processes that drive physiological cell-type diversity. As cancer types and subtypes arise from different cell types, we investigated whether cellular differentiation influences intratumor heterogeneity. Nodal B-cell non-Hodgkin lymphomas are a diverse set of cancers originating from different stages of B-cell maturation. Through single-cell transcriptome and surface epitope profiling (CITE-Seq) of diffuse large B-cell, mantle cell, follicular, and marginal zone lymphomas in addition to reactive lymph nodes from 51 patients, we found multiple B-cell maturation states within tumors. Intratumor maturation states emerged from the same clone, revealing divergent differentiation from a shared cell of origin. Maturation state composition varied across subtypes and tumors, which encompassed mixed cell-of-origin diagnostic subtypes. Through highly multiplexed immunohistochemistry (CODEX) of samples from 19 of these patients, we found that intratumor maturation states inhabited distinct spatial niches, displaying cellular interactions and regulatory networks typical of their maturation states while harboring different genetic variants. By deconvoluting intratumor maturation states from a microarray dataset of 507 patients, we identified risk groups within diagnoses with striking differences in survival, including IgM memory-enriched germinal center B-cell (M = 1.9 vs >10 years, p = 0.00039) and activated B-cell (M = 2.4 vs 9.6 years, p = 0.016) diffuse large B-cell lymphoma, and dark zone-enriched follicular lymphoma (M = 8.6 vs 13 years; p = 0.0019). Our findings reveal cellular differentiation remains plastic in B-cell lymphomas, driving tumor variation, evolution, and response. Key PointsO_LICellular differentiation remains plastic in B-cell lymphomas, driving tumor variation, evolution, and response. C_LIO_LIIntratumor maturation states occupy unique immune niches, harbor distinct genetic variants, and are tied to different survival outcomes. C_LI

cancer biology↗