Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study

Abstract Circulating plasma and peripheral blood mononuclear (PBMCs) cells provide an informative snapshot of the systemic physiological state. Moreover, they provide a non-invasively accessible compartment to identify biomarkers for personalized medicine in advanced breast cancer. The role of Neuro...

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Autores principales: Adviti Naik, Noura Al-Zeheimi, Charles Saki Bakheit, Marwa Al Riyami, Adil Al Jarrah, Mansour S. Al Moundhri, Zamzam Al Habsi, Maysoon Basheer, Sirin A. Adham
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/087d3ded70bd4d49b2929792f742aed6
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spelling oai:doaj.org-article:087d3ded70bd4d49b2929792f742aed62021-12-02T12:32:13ZNeuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study10.1038/s41598-017-03280-02045-2322https://doaj.org/article/087d3ded70bd4d49b2929792f742aed62017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03280-0https://doaj.org/toc/2045-2322Abstract Circulating plasma and peripheral blood mononuclear (PBMCs) cells provide an informative snapshot of the systemic physiological state. Moreover, they provide a non-invasively accessible compartment to identify biomarkers for personalized medicine in advanced breast cancer. The role of Neuropilin-1 (NRP-1) and its interacting molecules in breast tumor tissue was correlated with cancer progression; however, the clinical impact of their systemic levels was not extensively evaluated. In this cross-sectional study, we found that circulating and tumor tissue expression of NRP-1 and circulating placental growth factor (PlGF) increase in advanced nodal and metastatic breast cancer compared with locally advanced disease. Tumor tissue expression of NRP-1 and PlGF is also upregulated in triple negative breast cancer (TNBC) compared to other subtypes. Conversely, in PBMCs, NRP-1 and its interacting molecules SEMA4A and SNAI1 are significantly downregulated in breast cancer patients compared to healthy controls, indicating a protective role. Moreover, we report differential PBMC expression profiles that correlate inversely with disease stage (SEMA4A, SNAI1, PLXNA1 and VEGFR3) and can differentiate between the TNBC and non-TNBC tumor subtypes (VEGFR3 and PLXNA1). This work supports the importance of NRP-1-associated molecules in circulation to characterize poor prognosis breast cancer and emphasizes on their role as favorable drug targets.Adviti NaikNoura Al-ZeheimiCharles Saki BakheitMarwa Al RiyamiAdil Al JarrahMansour S. Al MoundhriZamzam Al HabsiMaysoon BasheerSirin A. AdhamNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Adviti Naik
Noura Al-Zeheimi
Charles Saki Bakheit
Marwa Al Riyami
Adil Al Jarrah
Mansour S. Al Moundhri
Zamzam Al Habsi
Maysoon Basheer
Sirin A. Adham
Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
description Abstract Circulating plasma and peripheral blood mononuclear (PBMCs) cells provide an informative snapshot of the systemic physiological state. Moreover, they provide a non-invasively accessible compartment to identify biomarkers for personalized medicine in advanced breast cancer. The role of Neuropilin-1 (NRP-1) and its interacting molecules in breast tumor tissue was correlated with cancer progression; however, the clinical impact of their systemic levels was not extensively evaluated. In this cross-sectional study, we found that circulating and tumor tissue expression of NRP-1 and circulating placental growth factor (PlGF) increase in advanced nodal and metastatic breast cancer compared with locally advanced disease. Tumor tissue expression of NRP-1 and PlGF is also upregulated in triple negative breast cancer (TNBC) compared to other subtypes. Conversely, in PBMCs, NRP-1 and its interacting molecules SEMA4A and SNAI1 are significantly downregulated in breast cancer patients compared to healthy controls, indicating a protective role. Moreover, we report differential PBMC expression profiles that correlate inversely with disease stage (SEMA4A, SNAI1, PLXNA1 and VEGFR3) and can differentiate between the TNBC and non-TNBC tumor subtypes (VEGFR3 and PLXNA1). This work supports the importance of NRP-1-associated molecules in circulation to characterize poor prognosis breast cancer and emphasizes on their role as favorable drug targets.
format article
author Adviti Naik
Noura Al-Zeheimi
Charles Saki Bakheit
Marwa Al Riyami
Adil Al Jarrah
Mansour S. Al Moundhri
Zamzam Al Habsi
Maysoon Basheer
Sirin A. Adham
author_facet Adviti Naik
Noura Al-Zeheimi
Charles Saki Bakheit
Marwa Al Riyami
Adil Al Jarrah
Mansour S. Al Moundhri
Zamzam Al Habsi
Maysoon Basheer
Sirin A. Adham
author_sort Adviti Naik
title Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
title_short Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
title_full Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
title_fullStr Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
title_full_unstemmed Neuropilin-1 Associated Molecules in the Blood Distinguish Poor Prognosis Breast Cancer: A Cross-Sectional Study
title_sort neuropilin-1 associated molecules in the blood distinguish poor prognosis breast cancer: a cross-sectional study
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/087d3ded70bd4d49b2929792f742aed6
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