Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?

Introduction: Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are involved in the progression of several tumors, including breast cancer. Our aim was to investigate the association of immunohistochemical expression of protein MMP-2, and -9 and tissue inhibitors T...

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Main Authors: Suada Kuskunović-Vlahovljak, Nina Čamdžić, Svjetlana Radović, Mirsad Dorić, Mirsad Babić, Edina Lazović Salčin, Lejla Džananović
Format: Article
Language:English
Published: University of Sarajevo 2017-12-01
Series:Journal of Health Sciences
Subjects:
Online Access:https://www.jhsci.ba/ojs/index.php/jhsci/article/view/620
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author Suada Kuskunović-Vlahovljak
Nina Čamdžić
Svjetlana Radović
Mirsad Dorić
Mirsad Babić
Edina Lazović Salčin
Lejla Džananović
author_facet Suada Kuskunović-Vlahovljak
Nina Čamdžić
Svjetlana Radović
Mirsad Dorić
Mirsad Babić
Edina Lazović Salčin
Lejla Džananović
author_sort Suada Kuskunović-Vlahovljak
collection DOAJ
description Introduction: Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are involved in the progression of several tumors, including breast cancer. Our aim was to investigate the association of immunohistochemical expression of protein MMP-2, and -9 and tissue inhibitors TIMP-1,-2,-3 by tumoral cells in the process of angiogenesis and to define their relation with clinicopathological features for breast cancer. Methods: Immunohistochemical analysis of MMP-2,-9, TIMP-1,-2,-3, endoglin/CD105, estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) status was performed on 79 tissue samples of breast cancer with axillary lymph node dissection. Results: Statistically significant difference was found between mean age of patients and tissue inhibitors of metalloproteinase (TIMP-1) expression status (p=0.008), i.e., women with TIMP-1 negative tumors were on average younger (mean age 46.5) compared to women with TIMP-1 positive tumors (mean age 58.1); TIMP-2 expression status showed association with ER status (p=0.017), while TIMP-3 negative tumors were on average more frequently ER and PR negative (p=0.016; p=0.027). Status of protein expression of MMP-9 was associated with TIMP-1 protein expression status (p=0.033), i.e., breast cancers with overexpression of protein MMP-9 were more frequently TIMP-1 protein positive. Conclusion: Only TIMPs were associated with clinicopathological features for breast cancer. TIMP-2 expression was associated with worse (TIMP-2 positive tumors were frequently ER-negative), while TIMP-3 expression in tumoral cells was associated with better clinicopathological features for breast cancer (TIMP-3 positive tumors were frequently ER and PR positive).
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spelling doaj.art-e9a773b0e20d43b1a3069f8a7a71d2f32022-12-21T21:17:34ZengUniversity of SarajevoJournal of Health Sciences2232-75761986-80492017-12-017310.17532/jhsci.2017.460Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?Suada Kuskunović-Vlahovljak0Nina Čamdžić1Svjetlana Radović2Mirsad Dorić3Mirsad Babić4Edina Lazović Salčin5Lejla Džananović6Department of Pathology, School of Medicine, University of SarajevoDepartment of Pathology, School of Medicine, University of SarajevoDepartment of Pathology, School of Medicine, University of SarajevoDepartment of Pathology, School of Medicine, University of SarajevoDepartment of Pathology, School of Medicine, University of SarajevoDepartment of Pathology, School of Medicine, University of SarajevoDepartment of Epidemiology and Biostatistics, School of Medicine, University of SarajevoIntroduction: Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are involved in the progression of several tumors, including breast cancer. Our aim was to investigate the association of immunohistochemical expression of protein MMP-2, and -9 and tissue inhibitors TIMP-1,-2,-3 by tumoral cells in the process of angiogenesis and to define their relation with clinicopathological features for breast cancer. Methods: Immunohistochemical analysis of MMP-2,-9, TIMP-1,-2,-3, endoglin/CD105, estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) status was performed on 79 tissue samples of breast cancer with axillary lymph node dissection. Results: Statistically significant difference was found between mean age of patients and tissue inhibitors of metalloproteinase (TIMP-1) expression status (p=0.008), i.e., women with TIMP-1 negative tumors were on average younger (mean age 46.5) compared to women with TIMP-1 positive tumors (mean age 58.1); TIMP-2 expression status showed association with ER status (p=0.017), while TIMP-3 negative tumors were on average more frequently ER and PR negative (p=0.016; p=0.027). Status of protein expression of MMP-9 was associated with TIMP-1 protein expression status (p=0.033), i.e., breast cancers with overexpression of protein MMP-9 were more frequently TIMP-1 protein positive. Conclusion: Only TIMPs were associated with clinicopathological features for breast cancer. TIMP-2 expression was associated with worse (TIMP-2 positive tumors were frequently ER-negative), while TIMP-3 expression in tumoral cells was associated with better clinicopathological features for breast cancer (TIMP-3 positive tumors were frequently ER and PR positive).https://www.jhsci.ba/ojs/index.php/jhsci/article/view/620Breast cancermatrix metalloproteinasestissue inhibitors of metalloproteinasesangiogenesisendoglinimmunohistochemistry
spellingShingle Suada Kuskunović-Vlahovljak
Nina Čamdžić
Svjetlana Radović
Mirsad Dorić
Mirsad Babić
Edina Lazović Salčin
Lejla Džananović
Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
Journal of Health Sciences
Breast cancer
matrix metalloproteinases
tissue inhibitors of metalloproteinases
angiogenesis
endoglin
immunohistochemistry
title Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
title_full Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
title_fullStr Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
title_full_unstemmed Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
title_short Is the expression of matrix metalloproteinases (MMP-2, -9) and tissue inhibitors of metalloproteinases (TIMP-1, -2, and -3) associated with angiogenesis and clinicopathological features for breast cancer?
title_sort is the expression of matrix metalloproteinases mmp 2 9 and tissue inhibitors of metalloproteinases timp 1 2 and 3 associated with angiogenesis and clinicopathological features for breast cancer
topic Breast cancer
matrix metalloproteinases
tissue inhibitors of metalloproteinases
angiogenesis
endoglin
immunohistochemistry
url https://www.jhsci.ba/ojs/index.php/jhsci/article/view/620
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