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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Main Authors: 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
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/4/906
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spelling 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
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