The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer

Research on tumor angiogenesis has mainly focused on the vascular endothelial growth factor (VEGF) family and on methods to block its actions. However, reports on VEGF receptor (VEGFR) expression in tumor-associated endothelial cells (ECs) are limited. Thus, we evaluated VEGF, VEGFR-1 and VEGFR-2 ex...

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Main Authors: Nicky D’Haene, Caroline Koopmansch, Yves-Rémi Van Eycke, Françoise Hulet, Justine Allard, Sarah Bouri, Sandrine Rorive, Myriam Remmelink, Christine Decaestecker, Calliope Maris, Isabelle Salmon
Format: Article
Language:English
Published: MDPI AG 2018-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/19/11/3536
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spelling doaj-0c7e31e910654402a5f35829a5c00b0e2020-11-25T00:34:54ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-11-011911353610.3390/ijms19113536ijms19113536The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal CancerNicky D’Haene0Caroline Koopmansch1Yves-Rémi Van Eycke2Françoise Hulet3Justine Allard4Sarah Bouri5Sandrine Rorive6Myriam Remmelink7Christine Decaestecker8Calliope Maris9Isabelle Salmon10Department of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDIAPath—Center for Microscopy and Molecular Imaging, ULB, 6041 Gosselies, BelgiumCMP-Cerba European Labs, 1070 Brussels, BelgiumDIAPath—Center for Microscopy and Molecular Imaging, ULB, 6041 Gosselies, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDIAPath—Center for Microscopy and Molecular Imaging, ULB, 6041 Gosselies, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles (ULB),1070 Brussels, BelgiumResearch on tumor angiogenesis has mainly focused on the vascular endothelial growth factor (VEGF) family and on methods to block its actions. However, reports on VEGF receptor (VEGFR) expression in tumor-associated endothelial cells (ECs) are limited. Thus, we evaluated VEGF, VEGFR-1 and VEGFR-2 expression in ECs of colorectal cancer (CRC) using immunohistochemistry. VEGF, VEGFR-1 and -2 expression in ECs was quantitatively evaluated by digital image analysis in a retrospective series of 204 tumor tissue samples and related to clinical variables. The data show that the VEGF, VEGFR-1 and VEGFR-2 expression in ECs is heterogeneous. Multivariate analysis including a set of clinicopathological variables reveals that high EC VEGFR-1 expression is an independent prognostic factor for overall survival (OS). The combination of low VEGFR-1 and high VEGFR-2 expression in ECs outperforms models integrating VEGFR-1 and VEGFR-2 as separate markers. Indeed, this VEGFR-1_VEGFR-2 combination is an independent negative prognostic factor for OS (<i>p</i> = 0.012) and metastasis-free survival (<i>p</i> = 0.007). In conclusion, this work illustrates the importance of studying the distribution of VEGF members in ECs of CRC. Interestingly, our preliminary data suggest that high VEGFR-1 and low VEGFR-2 expression in ECs appear to be involved in the progression of CRC, suggesting that targeting EC VEGFR-1 could offer novel opportunities for CRC treatment. However, a prospective validation study is needed.https://www.mdpi.com/1422-0067/19/11/3536VEGFR-1VEGFR-2endothelial cellscolorectal cancerprognosis
collection DOAJ
language English
format Article
sources DOAJ
author Nicky D’Haene
Caroline Koopmansch
Yves-Rémi Van Eycke
Françoise Hulet
Justine Allard
Sarah Bouri
Sandrine Rorive
Myriam Remmelink
Christine Decaestecker
Calliope Maris
Isabelle Salmon
spellingShingle Nicky D’Haene
Caroline Koopmansch
Yves-Rémi Van Eycke
Françoise Hulet
Justine Allard
Sarah Bouri
Sandrine Rorive
Myriam Remmelink
Christine Decaestecker
Calliope Maris
Isabelle Salmon
The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
International Journal of Molecular Sciences
VEGFR-1
VEGFR-2
endothelial cells
colorectal cancer
prognosis
author_facet Nicky D’Haene
Caroline Koopmansch
Yves-Rémi Van Eycke
Françoise Hulet
Justine Allard
Sarah Bouri
Sandrine Rorive
Myriam Remmelink
Christine Decaestecker
Calliope Maris
Isabelle Salmon
author_sort Nicky D’Haene
title The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
title_short The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
title_full The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
title_fullStr The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
title_full_unstemmed The Prognostic Value of the Combination of Low VEGFR-1 and High VEGFR-2 Expression in Endothelial Cells of Colorectal Cancer
title_sort prognostic value of the combination of low vegfr-1 and high vegfr-2 expression in endothelial cells of colorectal cancer
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-11-01
description Research on tumor angiogenesis has mainly focused on the vascular endothelial growth factor (VEGF) family and on methods to block its actions. However, reports on VEGF receptor (VEGFR) expression in tumor-associated endothelial cells (ECs) are limited. Thus, we evaluated VEGF, VEGFR-1 and VEGFR-2 expression in ECs of colorectal cancer (CRC) using immunohistochemistry. VEGF, VEGFR-1 and -2 expression in ECs was quantitatively evaluated by digital image analysis in a retrospective series of 204 tumor tissue samples and related to clinical variables. The data show that the VEGF, VEGFR-1 and VEGFR-2 expression in ECs is heterogeneous. Multivariate analysis including a set of clinicopathological variables reveals that high EC VEGFR-1 expression is an independent prognostic factor for overall survival (OS). The combination of low VEGFR-1 and high VEGFR-2 expression in ECs outperforms models integrating VEGFR-1 and VEGFR-2 as separate markers. Indeed, this VEGFR-1_VEGFR-2 combination is an independent negative prognostic factor for OS (<i>p</i> = 0.012) and metastasis-free survival (<i>p</i> = 0.007). In conclusion, this work illustrates the importance of studying the distribution of VEGF members in ECs of CRC. Interestingly, our preliminary data suggest that high VEGFR-1 and low VEGFR-2 expression in ECs appear to be involved in the progression of CRC, suggesting that targeting EC VEGFR-1 could offer novel opportunities for CRC treatment. However, a prospective validation study is needed.
topic VEGFR-1
VEGFR-2
endothelial cells
colorectal cancer
prognosis
url https://www.mdpi.com/1422-0067/19/11/3536
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