A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker
In cancer biology, epithelial-to-mesenchymal transition (EMT) is associated with tumorigenesis, stemness, invasion, metastasis, and resistance to therapy. Evidence of co-expression of epithelial and mesenchymal markers suggests that EMT should be a stepwise process with distinct intermediate states...
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doaj-54d04fe499f44faeb5567c5edd1bb0e02020-11-25T02:43:22ZengMDPI AGCancers2072-66942020-04-011290690610.3390/cancers12040906A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic MarkerLouis Godin0Cédric Balsat1Yves-Rémi Van Eycke2Justine Allard3Claire Royer4Myriam Remmelink5Ievgenia Pastushenko6Nicky D’Haene7Cédric Blanpain8Isabelle Salmon9Sandrine Rorive10Christine Decaestecker11Department of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDIAPath, Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles (ULB), CPI 305/1, Rue Adrienne Bolland, 8, 6041 Gosselies, BelgiumDIAPath, Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles (ULB), CPI 305/1, Rue Adrienne Bolland, 8, 6041 Gosselies, BelgiumDIAPath, Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles (ULB), CPI 305/1, Rue Adrienne Bolland, 8, 6041 Gosselies, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, BelgiumDIAPath, Center for Microscopy and Molecular Imaging, Université Libre de Bruxelles (ULB), CPI 305/1, Rue Adrienne Bolland, 8, 6041 Gosselies, BelgiumIn cancer biology, epithelial-to-mesenchymal transition (EMT) is associated with tumorigenesis, stemness, invasion, metastasis, and resistance to therapy. Evidence of co-expression of epithelial and mesenchymal markers suggests that EMT should be a stepwise process with distinct intermediate states rather than a binary switch. In the present study, we propose a morphological approach that enables the detection and quantification of cancer cells with hybrid E/M states, i.e., which combine partially epithelial (E) and partially mesenchymal (M) states. This approach is based on a sequential immunohistochemistry technique performed on the same tissue section, the digitization of whole slides, and image processing. The aim is to extract quantitative indicators able to quantify the presence of hybrid E/M states in large series of human cancer samples and to analyze their relationship with cancer aggressiveness. As a proof of concept, we applied our methodology to a series of about a hundred urothelial carcinomas and demonstrated that the presence of cancer cells with hybrid E/M phenotypes at the time of diagnosis is strongly associated with a poor prognostic value, independently of standard clinicopathological features. Although validation on a larger case series and other cancer types is required, our data support the hybrid E/M score as a promising prognostic biomarker for carcinoma patients.https://www.mdpi.com/2072-6694/12/4/906computational pathologyhybrid E/M statepartial EMTprognosisquantificationsequential immunohistochemistry |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Louis Godin Cédric Balsat Yves-Rémi Van Eycke Justine Allard Claire Royer Myriam Remmelink Ievgenia Pastushenko Nicky D’Haene Cédric Blanpain Isabelle Salmon Sandrine Rorive Christine Decaestecker |
spellingShingle |
Louis Godin Cédric Balsat Yves-Rémi Van Eycke Justine Allard Claire Royer Myriam Remmelink Ievgenia Pastushenko Nicky D’Haene Cédric Blanpain Isabelle Salmon Sandrine Rorive Christine Decaestecker A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker Cancers computational pathology hybrid E/M state partial EMT prognosis quantification sequential immunohistochemistry |
author_facet |
Louis Godin Cédric Balsat Yves-Rémi Van Eycke Justine Allard Claire Royer Myriam Remmelink Ievgenia Pastushenko Nicky D’Haene Cédric Blanpain Isabelle Salmon Sandrine Rorive Christine Decaestecker |
author_sort |
Louis Godin |
title |
A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker |
title_short |
A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker |
title_full |
A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker |
title_fullStr |
A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker |
title_full_unstemmed |
A Novel Approach for Quantifying Cancer Cells Showing Hybrid Epithelial/Mesenchymal States in Large Series of Tissue Samples: Towards a New Prognostic Marker |
title_sort |
novel approach for quantifying cancer cells showing hybrid epithelial/mesenchymal states in large series of tissue samples: towards a new prognostic marker |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2020-04-01 |
description |
In cancer biology, epithelial-to-mesenchymal transition (EMT) is associated with tumorigenesis, stemness, invasion, metastasis, and resistance to therapy. Evidence of co-expression of epithelial and mesenchymal markers suggests that EMT should be a stepwise process with distinct intermediate states rather than a binary switch. In the present study, we propose a morphological approach that enables the detection and quantification of cancer cells with hybrid E/M states, i.e., which combine partially epithelial (E) and partially mesenchymal (M) states. This approach is based on a sequential immunohistochemistry technique performed on the same tissue section, the digitization of whole slides, and image processing. The aim is to extract quantitative indicators able to quantify the presence of hybrid E/M states in large series of human cancer samples and to analyze their relationship with cancer aggressiveness. As a proof of concept, we applied our methodology to a series of about a hundred urothelial carcinomas and demonstrated that the presence of cancer cells with hybrid E/M phenotypes at the time of diagnosis is strongly associated with a poor prognostic value, independently of standard clinicopathological features. Although validation on a larger case series and other cancer types is required, our data support the hybrid E/M score as a promising prognostic biomarker for carcinoma patients. |
topic |
computational pathology hybrid E/M state partial EMT prognosis quantification sequential immunohistochemistry |
url |
https://www.mdpi.com/2072-6694/12/4/906 |
work_keys_str_mv |
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