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...
Guardado en:
Autores principales: | , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/087d3ded70bd4d49b2929792f742aed6 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:087d3ded70bd4d49b2929792f742aed6 |
---|---|
record_format |
dspace |
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 |
work_keys_str_mv |
AT advitinaik neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT nouraalzeheimi neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT charlessakibakheit neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT marwaalriyami neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT adilaljarrah neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT mansoursalmoundhri neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT zamzamalhabsi neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT maysoonbasheer neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy AT sirinaadham neuropilin1associatedmoleculesintheblooddistinguishpoorprognosisbreastcanceracrosssectionalstudy |
_version_ |
1718394138851803136 |