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Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis

BACKGROUND: Canine visceral hemangiosarcoma (HSA) is a highly aggressive cancer of endothelial origin that closely resembles visceral angiosarcoma in humans, both clinically and histopathologically. Currently there is an unmet need for new diagnostics and therapies for both forms of this disease. Th...

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Autores principales: Mukai, Chinatsu, Choi, Eunju, Sams, Kelly L., Klampen, Elena Zu, Anguish, Lynne, Marks, Brooke A., Rice, Edward J., Wang, Zhong, Choate, Lauren A., Chou, Shao-Pei, Kato, Yukinari, Miller, Andrew D., Danko, Charles G., Coonrod, Scott A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310061/
https://www.ncbi.nlm.nih.gov/pubmed/32571313
http://dx.doi.org/10.1186/s12917-020-02395-3
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author Mukai, Chinatsu
Choi, Eunju
Sams, Kelly L.
Klampen, Elena Zu
Anguish, Lynne
Marks, Brooke A.
Rice, Edward J.
Wang, Zhong
Choate, Lauren A.
Chou, Shao-Pei
Kato, Yukinari
Miller, Andrew D.
Danko, Charles G.
Coonrod, Scott A.
author_facet Mukai, Chinatsu
Choi, Eunju
Sams, Kelly L.
Klampen, Elena Zu
Anguish, Lynne
Marks, Brooke A.
Rice, Edward J.
Wang, Zhong
Choate, Lauren A.
Chou, Shao-Pei
Kato, Yukinari
Miller, Andrew D.
Danko, Charles G.
Coonrod, Scott A.
author_sort Mukai, Chinatsu
collection PubMed
description BACKGROUND: Canine visceral hemangiosarcoma (HSA) is a highly aggressive cancer of endothelial origin that closely resembles visceral angiosarcoma in humans, both clinically and histopathologically. Currently there is an unmet need for new diagnostics and therapies for both forms of this disease. The goal of this study was to utilize Chromatin run-on sequencing (ChRO-seq) and immunohistochemistry (IHC) to identify gene and protein expression signatures that may be important drivers of HSA progression. RESULTS: ChRO-seq was performed on tissue isolated from 17 HSA samples and 4 normal splenic samples. Computational analysis was then used to identify differentially expressed genes and these factors were subjected to gene ontology analysis. ChRO-seq analysis revealed over a thousand differentially expressed genes in HSA tissue compared with normal splenic tissue (FDR < 0.005). Interestingly, the majority of genes overexpressed in HSA tumor tissue were associated with extracellular matrix (ECM) remodeling. This observation correlated well with our histological analysis, which found that HSA tumors contain a rich and complex collagen network. Additionally, we characterized the protein expression patterns of two highly overexpressed molecules identified in ChRO-seq analysis, podoplanin (PDPN) and laminin alpha 4 (LAMA4). We found that the expression of these two ECM-associated factors appeared to be largely limited to transformed endothelial cells within the HSA lesions. CONCLUSION: Outcomes from this study suggest that ECM remodeling plays an important role in HSA progression. Additionally, our study identified two potential novel biomarkers of HSA, PDPN and LAMA4. Interestingly, given that function-blocking anti-PDPN antibodies have shown anti-tumor effects in mouse models of canine melanoma, our studies raise the possibility that these types of therapeutic strategies could potentially be developed for treating canine HSA.
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spelling pubmed-73100612020-06-23 Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis Mukai, Chinatsu Choi, Eunju Sams, Kelly L. Klampen, Elena Zu Anguish, Lynne Marks, Brooke A. Rice, Edward J. Wang, Zhong Choate, Lauren A. Chou, Shao-Pei Kato, Yukinari Miller, Andrew D. Danko, Charles G. Coonrod, Scott A. BMC Vet Res Research Article BACKGROUND: Canine visceral hemangiosarcoma (HSA) is a highly aggressive cancer of endothelial origin that closely resembles visceral angiosarcoma in humans, both clinically and histopathologically. Currently there is an unmet need for new diagnostics and therapies for both forms of this disease. The goal of this study was to utilize Chromatin run-on sequencing (ChRO-seq) and immunohistochemistry (IHC) to identify gene and protein expression signatures that may be important drivers of HSA progression. RESULTS: ChRO-seq was performed on tissue isolated from 17 HSA samples and 4 normal splenic samples. Computational analysis was then used to identify differentially expressed genes and these factors were subjected to gene ontology analysis. ChRO-seq analysis revealed over a thousand differentially expressed genes in HSA tissue compared with normal splenic tissue (FDR < 0.005). Interestingly, the majority of genes overexpressed in HSA tumor tissue were associated with extracellular matrix (ECM) remodeling. This observation correlated well with our histological analysis, which found that HSA tumors contain a rich and complex collagen network. Additionally, we characterized the protein expression patterns of two highly overexpressed molecules identified in ChRO-seq analysis, podoplanin (PDPN) and laminin alpha 4 (LAMA4). We found that the expression of these two ECM-associated factors appeared to be largely limited to transformed endothelial cells within the HSA lesions. CONCLUSION: Outcomes from this study suggest that ECM remodeling plays an important role in HSA progression. Additionally, our study identified two potential novel biomarkers of HSA, PDPN and LAMA4. Interestingly, given that function-blocking anti-PDPN antibodies have shown anti-tumor effects in mouse models of canine melanoma, our studies raise the possibility that these types of therapeutic strategies could potentially be developed for treating canine HSA. BioMed Central 2020-06-22 /pmc/articles/PMC7310061/ /pubmed/32571313 http://dx.doi.org/10.1186/s12917-020-02395-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Mukai, Chinatsu
Choi, Eunju
Sams, Kelly L.
Klampen, Elena Zu
Anguish, Lynne
Marks, Brooke A.
Rice, Edward J.
Wang, Zhong
Choate, Lauren A.
Chou, Shao-Pei
Kato, Yukinari
Miller, Andrew D.
Danko, Charles G.
Coonrod, Scott A.
Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title_full Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title_fullStr Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title_full_unstemmed Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title_short Chromatin run-on sequencing analysis finds that ECM remodeling plays an important role in canine hemangiosarcoma pathogenesis
title_sort chromatin run-on sequencing analysis finds that ecm remodeling plays an important role in canine hemangiosarcoma pathogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310061/
https://www.ncbi.nlm.nih.gov/pubmed/32571313
http://dx.doi.org/10.1186/s12917-020-02395-3
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