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Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients

BACKGROUND: Stromal and collagen biology has a significant impact on tumorigenesis and metastasis. Collagen is a major structural extracellular matrix component in breast cancer, but its role in cancer progression is the subject of historical debate. Collagen may represent a protective layer that pr...

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Autores principales: Gole, Laurent, Yeong, Joe, Lim, Jeffrey Chun Tatt, Ong, Kok Haur, Han, Hao, Thike, Aye Aye, Poh, Yong Cheng, Yee, Sidney, Iqbal, Jabed, Hong, Wanjin, Lee, Bernett, Yu, Weimiao, Tan, Puay Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204022/
https://www.ncbi.nlm.nih.gov/pubmed/32375854
http://dx.doi.org/10.1186/s13058-020-01282-x
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author Gole, Laurent
Yeong, Joe
Lim, Jeffrey Chun Tatt
Ong, Kok Haur
Han, Hao
Thike, Aye Aye
Poh, Yong Cheng
Yee, Sidney
Iqbal, Jabed
Hong, Wanjin
Lee, Bernett
Yu, Weimiao
Tan, Puay Hoon
author_facet Gole, Laurent
Yeong, Joe
Lim, Jeffrey Chun Tatt
Ong, Kok Haur
Han, Hao
Thike, Aye Aye
Poh, Yong Cheng
Yee, Sidney
Iqbal, Jabed
Hong, Wanjin
Lee, Bernett
Yu, Weimiao
Tan, Puay Hoon
author_sort Gole, Laurent
collection PubMed
description BACKGROUND: Stromal and collagen biology has a significant impact on tumorigenesis and metastasis. Collagen is a major structural extracellular matrix component in breast cancer, but its role in cancer progression is the subject of historical debate. Collagen may represent a protective layer that prevents cancer cell migration, while increased stromal collagen has been demonstrated to facilitate breast cancer metastasis. METHODS: Stromal remodeling is characterized by collagen fiber restructuring and realignment in stromal and tumoral areas. The patients in our study were diagnosed with triple-negative breast cancer in Singapore General Hospital from 2003 to 2015. We designed novel image processing and quantification pipelines to profile collagen structures using numerical imaging parameters. Our solution differentiated the collagen into two distinct modes: aggregated thick collagen (ATC) and dispersed thin collagen (DTC). RESULTS: Extracted parameters were significantly associated with bigger tumor size and DCIS association. Of numerical parameters, ATC collagen fiber density (CFD) and DTC collagen fiber length (CFL) were of significant prognostic value for disease-free survival and overall survival for the TNBC patient cohort. Using these two parameters, we built a predictive model to stratify the patients into four groups. CONCLUSIONS: Our study provides a novel insight for the quantitation of collagen in the tumor microenvironment and will help predict clinical outcomes for TNBC patients. The identified collagen parameters, ATC CFD and DTC CFL, represent a new direction for clinical prognosis and precision medicine. We also compared our result with benign samples and DICS samples to get novel insight about the TNBC heterogeneity. The improved understanding of collagen compartment of TNBC may provide insights into novel targets for better patient stratification and treatment.
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spelling pubmed-72040222020-05-12 Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients Gole, Laurent Yeong, Joe Lim, Jeffrey Chun Tatt Ong, Kok Haur Han, Hao Thike, Aye Aye Poh, Yong Cheng Yee, Sidney Iqbal, Jabed Hong, Wanjin Lee, Bernett Yu, Weimiao Tan, Puay Hoon Breast Cancer Res Research Article BACKGROUND: Stromal and collagen biology has a significant impact on tumorigenesis and metastasis. Collagen is a major structural extracellular matrix component in breast cancer, but its role in cancer progression is the subject of historical debate. Collagen may represent a protective layer that prevents cancer cell migration, while increased stromal collagen has been demonstrated to facilitate breast cancer metastasis. METHODS: Stromal remodeling is characterized by collagen fiber restructuring and realignment in stromal and tumoral areas. The patients in our study were diagnosed with triple-negative breast cancer in Singapore General Hospital from 2003 to 2015. We designed novel image processing and quantification pipelines to profile collagen structures using numerical imaging parameters. Our solution differentiated the collagen into two distinct modes: aggregated thick collagen (ATC) and dispersed thin collagen (DTC). RESULTS: Extracted parameters were significantly associated with bigger tumor size and DCIS association. Of numerical parameters, ATC collagen fiber density (CFD) and DTC collagen fiber length (CFL) were of significant prognostic value for disease-free survival and overall survival for the TNBC patient cohort. Using these two parameters, we built a predictive model to stratify the patients into four groups. CONCLUSIONS: Our study provides a novel insight for the quantitation of collagen in the tumor microenvironment and will help predict clinical outcomes for TNBC patients. The identified collagen parameters, ATC CFD and DTC CFL, represent a new direction for clinical prognosis and precision medicine. We also compared our result with benign samples and DICS samples to get novel insight about the TNBC heterogeneity. The improved understanding of collagen compartment of TNBC may provide insights into novel targets for better patient stratification and treatment. BioMed Central 2020-05-06 2020 /pmc/articles/PMC7204022/ /pubmed/32375854 http://dx.doi.org/10.1186/s13058-020-01282-x 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
Gole, Laurent
Yeong, Joe
Lim, Jeffrey Chun Tatt
Ong, Kok Haur
Han, Hao
Thike, Aye Aye
Poh, Yong Cheng
Yee, Sidney
Iqbal, Jabed
Hong, Wanjin
Lee, Bernett
Yu, Weimiao
Tan, Puay Hoon
Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title_full Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title_fullStr Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title_full_unstemmed Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title_short Quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
title_sort quantitative stain-free imaging and digital profiling of collagen structure reveal diverse survival of triple negative breast cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204022/
https://www.ncbi.nlm.nih.gov/pubmed/32375854
http://dx.doi.org/10.1186/s13058-020-01282-x
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