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The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification

BACKGROUND: Podoplanin (PDPN) is a type-1 membrane sialoglycoprotein that is expressed in many cancer tumors including breast cancer; nonetheless, its roles in tumor occurrence, development, and metastasis are unclear. In this study, we aimed to investigate the clinical significance of plasma solubl...

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Autores principales: Zhu, Xinyi, Xu, Mengqiao, Zhao, Xingpeng, Shen, Fei, Ruan, Changgeng, Zhao, Yiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767643/
https://www.ncbi.nlm.nih.gov/pubmed/33380828
http://dx.doi.org/10.2147/CMAR.S281785
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author Zhu, Xinyi
Xu, Mengqiao
Zhao, Xingpeng
Shen, Fei
Ruan, Changgeng
Zhao, Yiming
author_facet Zhu, Xinyi
Xu, Mengqiao
Zhao, Xingpeng
Shen, Fei
Ruan, Changgeng
Zhao, Yiming
author_sort Zhu, Xinyi
collection PubMed
description BACKGROUND: Podoplanin (PDPN) is a type-1 membrane sialoglycoprotein that is expressed in many cancer tumors including breast cancer; nonetheless, its roles in tumor occurrence, development, and metastasis are unclear. In this study, we aimed to investigate the clinical significance of plasma soluble PDPN (sPDPN) levels in patients with breast cancer and its significance in the diagnosis and metastasis. MATERIALS AND METHODS: Blood samples from healthy controls (CTL), patients with fibroadenomas of breast (FOB), and breast cancer (pathological type: invasive ductal carcinoma, IDC) were collected. sPDPN levels in the plasma of CTL and patients with FOB and IDC were measured by the ELISA. RESULTS: The plasma sPDPN levels in IDC patients (159 cases, 22.59±3.70 ng/mL) were higher than those in FOB patients (50 cases, 8.29±1.09 ng/mL; P<0.05) and CTL (100 cases, 1.21±0.12 ng/mL; P<0.0001). The sPDPN levels in patients at stage III and stage IV (30.08±4.66 ng/mL) were higher than in patients at stage I and stage II (11.84±1.12 ng/mL; P=0.005). The sPDPN levels in patients with high-moderate and moderate differentiation (17.50±3.02 ng/mL) were lower than those in patients with moderately low and low differentiation (35.73±4.26 ng/mL; P=0.026). The sPDPN levels in patients with metastasis (30.60±4.27 ng/mL) were much higher than those in patients without metastasis (13.02±1.30 ng/mL; P=0.017). CONCLUSION: Plasma sPDPN may be used as a new marker for the determination of the clinical stage, differentiation degree, and metastasis status of breast cancer.
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spelling pubmed-77676432020-12-29 The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification Zhu, Xinyi Xu, Mengqiao Zhao, Xingpeng Shen, Fei Ruan, Changgeng Zhao, Yiming Cancer Manag Res Original Research BACKGROUND: Podoplanin (PDPN) is a type-1 membrane sialoglycoprotein that is expressed in many cancer tumors including breast cancer; nonetheless, its roles in tumor occurrence, development, and metastasis are unclear. In this study, we aimed to investigate the clinical significance of plasma soluble PDPN (sPDPN) levels in patients with breast cancer and its significance in the diagnosis and metastasis. MATERIALS AND METHODS: Blood samples from healthy controls (CTL), patients with fibroadenomas of breast (FOB), and breast cancer (pathological type: invasive ductal carcinoma, IDC) were collected. sPDPN levels in the plasma of CTL and patients with FOB and IDC were measured by the ELISA. RESULTS: The plasma sPDPN levels in IDC patients (159 cases, 22.59±3.70 ng/mL) were higher than those in FOB patients (50 cases, 8.29±1.09 ng/mL; P<0.05) and CTL (100 cases, 1.21±0.12 ng/mL; P<0.0001). The sPDPN levels in patients at stage III and stage IV (30.08±4.66 ng/mL) were higher than in patients at stage I and stage II (11.84±1.12 ng/mL; P=0.005). The sPDPN levels in patients with high-moderate and moderate differentiation (17.50±3.02 ng/mL) were lower than those in patients with moderately low and low differentiation (35.73±4.26 ng/mL; P=0.026). The sPDPN levels in patients with metastasis (30.60±4.27 ng/mL) were much higher than those in patients without metastasis (13.02±1.30 ng/mL; P=0.017). CONCLUSION: Plasma sPDPN may be used as a new marker for the determination of the clinical stage, differentiation degree, and metastasis status of breast cancer. Dove 2020-12-23 /pmc/articles/PMC7767643/ /pubmed/33380828 http://dx.doi.org/10.2147/CMAR.S281785 Text en © 2020 Zhu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhu, Xinyi
Xu, Mengqiao
Zhao, Xingpeng
Shen, Fei
Ruan, Changgeng
Zhao, Yiming
The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title_full The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title_fullStr The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title_full_unstemmed The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title_short The Detection of Plasma Soluble Podoplanin of Patients with Breast Cancer and Its Clinical Signification
title_sort detection of plasma soluble podoplanin of patients with breast cancer and its clinical signification
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767643/
https://www.ncbi.nlm.nih.gov/pubmed/33380828
http://dx.doi.org/10.2147/CMAR.S281785
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