Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff

Background<p>Dynamic remodelling of the tumour microenvironment (TME) plays a central role in prostate cancer (PCa) progression, immune evasion and therapy resistance. However, the co-existence of both tumour-promoting and tumour-restraining stromal elements necessitates extensive characterisa...

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Glavni avtor: Elisabeth Damisch (22679276) (author)
Drugi avtorji: Elena Brunner (11153976) (author), Lukas Nommensen (22679279) (author), Lucy Neumann (22679282) (author), Georgios Fotakis (9598167) (author), Zlatko Trajanoski (15774) (author), Sieghart Sopper (823900) (author), Georg Schäfer (279214) (author), Martin Puhr (697731) (author), Isabel Heidegger (689987) (author), Marianna Kruithof-de Julio (9014339) (author), Natalie Sampson (6414767) (author)
Izdano: 2025
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author Elisabeth Damisch (22679276)
author2 Elena Brunner (11153976)
Lukas Nommensen (22679279)
Lucy Neumann (22679282)
Georgios Fotakis (9598167)
Zlatko Trajanoski (15774)
Sieghart Sopper (823900)
Georg Schäfer (279214)
Martin Puhr (697731)
Isabel Heidegger (689987)
Marianna Kruithof-de Julio (9014339)
Natalie Sampson (6414767)
author2_role author
author
author
author
author
author
author
author
author
author
author
author_facet Elisabeth Damisch (22679276)
Elena Brunner (11153976)
Lukas Nommensen (22679279)
Lucy Neumann (22679282)
Georgios Fotakis (9598167)
Zlatko Trajanoski (15774)
Sieghart Sopper (823900)
Georg Schäfer (279214)
Martin Puhr (697731)
Isabel Heidegger (689987)
Marianna Kruithof-de Julio (9014339)
Natalie Sampson (6414767)
author_role author
dc.creator.none.fl_str_mv Elisabeth Damisch (22679276)
Elena Brunner (11153976)
Lukas Nommensen (22679279)
Lucy Neumann (22679282)
Georgios Fotakis (9598167)
Zlatko Trajanoski (15774)
Sieghart Sopper (823900)
Georg Schäfer (279214)
Martin Puhr (697731)
Isabel Heidegger (689987)
Marianna Kruithof-de Julio (9014339)
Natalie Sampson (6414767)
dc.date.none.fl_str_mv 2025-11-25T06:25:27Z
dc.identifier.none.fl_str_mv 10.3389/fcell.2025.1653780.s008
dc.relation.none.fl_str_mv https://figshare.com/articles/figure/Image_3_Optimised_dissociation_and_multimodal_profiling_of_prostate_cancer_stroma_reveal_fibromuscular_cell_heterogeneity_with_clinical_correlates_tiff/30704093
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Cell Biology
cancer-associated fibroblast
prostate cancer
smooth muscle cell
tissue dissociation
single cell RNA sequencing
tumour microenvironment
dc.title.none.fl_str_mv Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
dc.type.none.fl_str_mv Image
Figure
info:eu-repo/semantics/publishedVersion
image
description Background<p>Dynamic remodelling of the tumour microenvironment (TME) plays a central role in prostate cancer (PCa) progression, immune evasion and therapy resistance. However, the co-existence of both tumour-promoting and tumour-restraining stromal elements necessitates extensive characterisation of the TME for effective targeting. Fibromuscular cell heterogeneity in PCa remains poorly characterised, in part due to challenges in isolating cells embedded within the desmoplastic stroma. This study therefore aimed to better characterise fibroblast and smooth muscle cell (SMC) populations as the major tissue-resident stromal cell subtypes within the PCa TME.</p>Methods<p>A PCa single-cell RNA sequencing (scRNA-seq) dataset was re-analysed to define fibromuscular subtypes. Due to low fibroblast yields, an optimised tissue dissociation protocol was developed and benchmarked against two commercial kits via flow cytometry, immunostaining of clinical specimens and ex vivo culture. Dimensionality reduction and clustering were applied to the CD31<sup>−</sup> stromal fraction using a multiparameter surface marker panel. Annotation of the resulting clusters based on their surface marker profile was supported by integrating scRNA-seq and immuno-histological findings.</p>Results<p>The optimised protocol yielded over twice the viable cells/mg tissue compared to two commercial kits, preserved surface marker integrity, enhanced successful cultivation of mesenchymal cells and recovered diverse stromal subpopulations from benign and malignant samples. Dimensionality reduction and clustering of flow cytometry counts identified 11 distinct CD31<sup>−</sup> stromal populations. Integration with transcriptomic data and immunofluorescence of clinical specimens identified spatially- and prognostically-distinct fibroblast subtypes, including inflammatory and myofibroblastic cancer-associated fibroblasts, pericytes linked to poor prognosis and a novel SMC subset associated with stromal activation.</p>Conclusion<p>This study presents a robust workflow for improved isolation and characterisation of fibromuscular stromal cells in PCa. The multimodal approach enabled refined characterisation of phenotypically distinct and clinically-relevant stromal subpopulations within their spatial context providing a foundation for future TME-targeted therapies.</p>
eu_rights_str_mv openAccess
id Manara_e705754e54e3f7066e04baacf6ebc517
identifier_str_mv 10.3389/fcell.2025.1653780.s008
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30704093
publishDate 2025
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repository.name.fl_str_mv
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rights_invalid_str_mv CC BY 4.0
spelling Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiffElisabeth Damisch (22679276)Elena Brunner (11153976)Lukas Nommensen (22679279)Lucy Neumann (22679282)Georgios Fotakis (9598167)Zlatko Trajanoski (15774)Sieghart Sopper (823900)Georg Schäfer (279214)Martin Puhr (697731)Isabel Heidegger (689987)Marianna Kruithof-de Julio (9014339)Natalie Sampson (6414767)Cell Biologycancer-associated fibroblastprostate cancersmooth muscle celltissue dissociationsingle cell RNA sequencingtumour microenvironmentBackground<p>Dynamic remodelling of the tumour microenvironment (TME) plays a central role in prostate cancer (PCa) progression, immune evasion and therapy resistance. However, the co-existence of both tumour-promoting and tumour-restraining stromal elements necessitates extensive characterisation of the TME for effective targeting. Fibromuscular cell heterogeneity in PCa remains poorly characterised, in part due to challenges in isolating cells embedded within the desmoplastic stroma. This study therefore aimed to better characterise fibroblast and smooth muscle cell (SMC) populations as the major tissue-resident stromal cell subtypes within the PCa TME.</p>Methods<p>A PCa single-cell RNA sequencing (scRNA-seq) dataset was re-analysed to define fibromuscular subtypes. Due to low fibroblast yields, an optimised tissue dissociation protocol was developed and benchmarked against two commercial kits via flow cytometry, immunostaining of clinical specimens and ex vivo culture. Dimensionality reduction and clustering were applied to the CD31<sup>−</sup> stromal fraction using a multiparameter surface marker panel. Annotation of the resulting clusters based on their surface marker profile was supported by integrating scRNA-seq and immuno-histological findings.</p>Results<p>The optimised protocol yielded over twice the viable cells/mg tissue compared to two commercial kits, preserved surface marker integrity, enhanced successful cultivation of mesenchymal cells and recovered diverse stromal subpopulations from benign and malignant samples. Dimensionality reduction and clustering of flow cytometry counts identified 11 distinct CD31<sup>−</sup> stromal populations. Integration with transcriptomic data and immunofluorescence of clinical specimens identified spatially- and prognostically-distinct fibroblast subtypes, including inflammatory and myofibroblastic cancer-associated fibroblasts, pericytes linked to poor prognosis and a novel SMC subset associated with stromal activation.</p>Conclusion<p>This study presents a robust workflow for improved isolation and characterisation of fibromuscular stromal cells in PCa. The multimodal approach enabled refined characterisation of phenotypically distinct and clinically-relevant stromal subpopulations within their spatial context providing a foundation for future TME-targeted therapies.</p>2025-11-25T06:25:27ZImageFigureinfo:eu-repo/semantics/publishedVersionimage10.3389/fcell.2025.1653780.s008https://figshare.com/articles/figure/Image_3_Optimised_dissociation_and_multimodal_profiling_of_prostate_cancer_stroma_reveal_fibromuscular_cell_heterogeneity_with_clinical_correlates_tiff/30704093CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307040932025-11-25T06:25:27Z
spellingShingle Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
Elisabeth Damisch (22679276)
Cell Biology
cancer-associated fibroblast
prostate cancer
smooth muscle cell
tissue dissociation
single cell RNA sequencing
tumour microenvironment
status_str publishedVersion
title Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
title_full Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
title_fullStr Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
title_full_unstemmed Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
title_short Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
title_sort Image 3_Optimised dissociation and multimodal profiling of prostate cancer stroma reveal fibromuscular cell heterogeneity with clinical correlates.tiff
topic Cell Biology
cancer-associated fibroblast
prostate cancer
smooth muscle cell
tissue dissociation
single cell RNA sequencing
tumour microenvironment