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Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data

In the tumor microenvironment (TME), functional interactions among tumor, immune, and stromal cells and the extracellular matrix play key roles in tumor progression, invasion, immune modulation, and response to treatment. Intratumor heterogeneity is ubiquitous not only at the genetic and transcripto...

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Autores principales: Biswas, Antara, Ghaddar, Bassel, Riedlinger, Gregory, De, Subhajyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410565/
https://www.ncbi.nlm.nih.gov/pubmed/36035873
http://dx.doi.org/10.1002/cso2.1043
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author Biswas, Antara
Ghaddar, Bassel
Riedlinger, Gregory
De, Subhajyoti
author_facet Biswas, Antara
Ghaddar, Bassel
Riedlinger, Gregory
De, Subhajyoti
author_sort Biswas, Antara
collection PubMed
description In the tumor microenvironment (TME), functional interactions among tumor, immune, and stromal cells and the extracellular matrix play key roles in tumor progression, invasion, immune modulation, and response to treatment. Intratumor heterogeneity is ubiquitous not only at the genetic and transcriptomic levels but also in the composition and characteristics of TME. However, quantitative inference on spatial heterogeneity in the TME is still limited. Here, we propose a framework to use network graph-based spatial statistical models on spatially annotated molecular data to gain insights into modularity and spatial heterogeneity in the TME. Applying the framework to spatial transcriptomics data from pancreatic ductal adenocarcinoma samples, we observed significant global and local spatially correlated patterns in the abundance score of tumor cells; in contrast, immune cell types showed dispersed patterns in the TME. Hypoxia, EMT, and inflammation signatures contributed to intra-tumor spatial variations. Spatial patterns in cell type abundance and pathway signatures in the TME potentially impact tumor growth dynamics and cancer hallmarks. Tumor biopsies are integral to the diagnosis and clinical management of cancer patients; our data suggest that owing to intra-tumor non-genetic spatial heterogeneity, individual biopsies may underappreciate the extent of clinically relevant, functional variations across geographic regions within tumors.
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spelling pubmed-94105652022-09-01 Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data Biswas, Antara Ghaddar, Bassel Riedlinger, Gregory De, Subhajyoti Comput Syst Oncol Article In the tumor microenvironment (TME), functional interactions among tumor, immune, and stromal cells and the extracellular matrix play key roles in tumor progression, invasion, immune modulation, and response to treatment. Intratumor heterogeneity is ubiquitous not only at the genetic and transcriptomic levels but also in the composition and characteristics of TME. However, quantitative inference on spatial heterogeneity in the TME is still limited. Here, we propose a framework to use network graph-based spatial statistical models on spatially annotated molecular data to gain insights into modularity and spatial heterogeneity in the TME. Applying the framework to spatial transcriptomics data from pancreatic ductal adenocarcinoma samples, we observed significant global and local spatially correlated patterns in the abundance score of tumor cells; in contrast, immune cell types showed dispersed patterns in the TME. Hypoxia, EMT, and inflammation signatures contributed to intra-tumor spatial variations. Spatial patterns in cell type abundance and pathway signatures in the TME potentially impact tumor growth dynamics and cancer hallmarks. Tumor biopsies are integral to the diagnosis and clinical management of cancer patients; our data suggest that owing to intra-tumor non-genetic spatial heterogeneity, individual biopsies may underappreciate the extent of clinically relevant, functional variations across geographic regions within tumors. 2022-09 2022-08-11 /pmc/articles/PMC9410565/ /pubmed/36035873 http://dx.doi.org/10.1002/cso2.1043 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Biswas, Antara
Ghaddar, Bassel
Riedlinger, Gregory
De, Subhajyoti
Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title_full Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title_fullStr Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title_full_unstemmed Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title_short Inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
title_sort inference on spatial heterogeneity in tumor microenvironment using spatial transcriptomics data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410565/
https://www.ncbi.nlm.nih.gov/pubmed/36035873
http://dx.doi.org/10.1002/cso2.1043
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AT desubhajyoti inferenceonspatialheterogeneityintumormicroenvironmentusingspatialtranscriptomicsdata