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High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast

PURPOSE: In the present study, we evaluated the levels of urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor 1 (PAI-1) by performing immunohistochemical staining to determine whether they were reliable prognostic markers in patients with breast cancer. METHODS: Demographi...

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Autores principales: Kim, Eun Young, Do, Sung-Im, Hyun, Keehoon, Park, Yong Lai, Kim, Dong-Hoon, Chae, Seoung Wan, Sohn, Jin Hee, Park, Chan Heun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Breast Cancer Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929256/
https://www.ncbi.nlm.nih.gov/pubmed/27382391
http://dx.doi.org/10.4048/jbc.2016.19.2.156
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author Kim, Eun Young
Do, Sung-Im
Hyun, Keehoon
Park, Yong Lai
Kim, Dong-Hoon
Chae, Seoung Wan
Sohn, Jin Hee
Park, Chan Heun
author_facet Kim, Eun Young
Do, Sung-Im
Hyun, Keehoon
Park, Yong Lai
Kim, Dong-Hoon
Chae, Seoung Wan
Sohn, Jin Hee
Park, Chan Heun
author_sort Kim, Eun Young
collection PubMed
description PURPOSE: In the present study, we evaluated the levels of urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor 1 (PAI-1) by performing immunohistochemical staining to determine whether they were reliable prognostic markers in patients with breast cancer. METHODS: Demographic and clinicopathological parameters of 214 patients with invasive ductal carcinoma (IDC) and 80 patients with ductal carcinoma in situ (DCIS) who were diagnosed and treated from 2006 to 2010 were analyzed. Tissue microarray was constructed and immunohistochemical staining was performed for each specimen. RESULTS: Univariate analyses showed that age at diagnosis, history of hormone replacement therapy, radiation therapy, skin and chest wall invasion, Paget disease, lymphovascular invasion, estrogen receptor positivity, and triple-negative subtype were significantly associated with patient prognosis (p<0.005). Patients with DCIS showed higher PAI-1 expression than patients with IDC (82.5% and 36.2%, respectively; p=0.012). Lymph node metastasis was more frequent in patients with high uPA levels than in patients with low uPA levels (p=0.001). CONCLUSION: Our results suggested that PAI-1 was involved in tumor progression in the early stages of breast cancer, such as DCIS. In addition, our results suggested that high uPA levels were associated with the lymph node metastasis of IDC.
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spelling pubmed-49292562016-07-05 High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast Kim, Eun Young Do, Sung-Im Hyun, Keehoon Park, Yong Lai Kim, Dong-Hoon Chae, Seoung Wan Sohn, Jin Hee Park, Chan Heun J Breast Cancer Original Article PURPOSE: In the present study, we evaluated the levels of urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor 1 (PAI-1) by performing immunohistochemical staining to determine whether they were reliable prognostic markers in patients with breast cancer. METHODS: Demographic and clinicopathological parameters of 214 patients with invasive ductal carcinoma (IDC) and 80 patients with ductal carcinoma in situ (DCIS) who were diagnosed and treated from 2006 to 2010 were analyzed. Tissue microarray was constructed and immunohistochemical staining was performed for each specimen. RESULTS: Univariate analyses showed that age at diagnosis, history of hormone replacement therapy, radiation therapy, skin and chest wall invasion, Paget disease, lymphovascular invasion, estrogen receptor positivity, and triple-negative subtype were significantly associated with patient prognosis (p<0.005). Patients with DCIS showed higher PAI-1 expression than patients with IDC (82.5% and 36.2%, respectively; p=0.012). Lymph node metastasis was more frequent in patients with high uPA levels than in patients with low uPA levels (p=0.001). CONCLUSION: Our results suggested that PAI-1 was involved in tumor progression in the early stages of breast cancer, such as DCIS. In addition, our results suggested that high uPA levels were associated with the lymph node metastasis of IDC. Korean Breast Cancer Society 2016-06 2016-06-24 /pmc/articles/PMC4929256/ /pubmed/27382391 http://dx.doi.org/10.4048/jbc.2016.19.2.156 Text en © 2016 Korean Breast Cancer Society. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Eun Young
Do, Sung-Im
Hyun, Keehoon
Park, Yong Lai
Kim, Dong-Hoon
Chae, Seoung Wan
Sohn, Jin Hee
Park, Chan Heun
High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title_full High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title_fullStr High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title_full_unstemmed High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title_short High Expression of Urokinase-Type Plasminogen Activator Is Associated with Lymph Node Metastasis of Invasive Ductal Carcinoma of the Breast
title_sort high expression of urokinase-type plasminogen activator is associated with lymph node metastasis of invasive ductal carcinoma of the breast
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929256/
https://www.ncbi.nlm.nih.gov/pubmed/27382391
http://dx.doi.org/10.4048/jbc.2016.19.2.156
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