Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers
Abstract Background MMP-7 and TIMP-1 may play a role in the pathogenesis of cancer disease. In this study we investigated plasma levels of selected metalloproteinase and its tissue inhibitor in comparison to plasma levels of the commonly accepted tumor markers (CA 125 and HE4) in selected histologic...
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doaj-2a00d012c9b34865b7fc20fed359c93e2020-11-24T21:14:28ZengBMCJournal of Ovarian Research1757-22152017-06-0110111010.1186/s13048-017-0338-zPlasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancersGrażyna Ewa Będkowska0Ewa Gacuta1Monika Zajkowska2Edyta Katarzyna Głażewska3Joanna Osada4Maciej Szmitkowski5Lech Chrostek6Milena Dąbrowska7Sławomir Ławicki8Department of Haematological Diagnostics, Medical University BialystokDepartment of Perinatology, Medical University BialystokDepartment of Biochemical Diagnostics, Medical University BialystokDepartment of Esthetic Medicine, Medical University BialystokDepartment of Haematological Diagnostics, Medical University BialystokDepartment of Biochemical Diagnostics, Medical University BialystokDepartment of Biochemical Diagnostics, Medical University BialystokDepartment of Haematological Diagnostics, Medical University BialystokDepartment of Biochemical Diagnostics, Medical University BialystokAbstract Background MMP-7 and TIMP-1 may play a role in the pathogenesis of cancer disease. In this study we investigated plasma levels of selected metalloproteinase and its tissue inhibitor in comparison to plasma levels of the commonly accepted tumor markers (CA 125 and HE4) in selected histological types of epithelial ovarian cancer patients as compared to control groups: patients with a benign ovarian tumor and healthy subjects. Plasma levels of MMP-7 and TIMP-1 were determined using ELISA, CA 125 and HE4 – by CMIA methods. Results Plasma levels of all biomarkers studied were significantly higher in ovarian cancer patients as compared to both control groups. MMP-7 demonstrated comparable to HE4 or CA125 values of diagnostic sensitivity (SE: 61%; 68%; 58%, respectively), specificity (SP: 95%; 95%; 98%, respectively), positive (PPV: 93%; 96%; 98%, respectively) and negative predictive values (NPV: 61%; 66%; 60%, respectively) in the groups tested. The combined use of the aforementioned biomarkers resulted in a further increase in diagnostic criteria and AUC, especially in the early stages of the disease. Conclusions These findings suggest the usefulness of combining MMP-7 with CA 125 and HE4 in the diagnosis of epithelial ovarian cancer as a new tumor marker panel.http://link.springer.com/article/10.1186/s13048-017-0338-zMMP-7TIMP-1HE4CA125Epithelial ovarian cancerTumor markers |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Grażyna Ewa Będkowska Ewa Gacuta Monika Zajkowska Edyta Katarzyna Głażewska Joanna Osada Maciej Szmitkowski Lech Chrostek Milena Dąbrowska Sławomir Ławicki |
spellingShingle |
Grażyna Ewa Będkowska Ewa Gacuta Monika Zajkowska Edyta Katarzyna Głażewska Joanna Osada Maciej Szmitkowski Lech Chrostek Milena Dąbrowska Sławomir Ławicki Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers Journal of Ovarian Research MMP-7 TIMP-1 HE4 CA125 Epithelial ovarian cancer Tumor markers |
author_facet |
Grażyna Ewa Będkowska Ewa Gacuta Monika Zajkowska Edyta Katarzyna Głażewska Joanna Osada Maciej Szmitkowski Lech Chrostek Milena Dąbrowska Sławomir Ławicki |
author_sort |
Grażyna Ewa Będkowska |
title |
Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
title_short |
Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
title_full |
Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
title_fullStr |
Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
title_full_unstemmed |
Plasma levels of MMP-7 and TIMP-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
title_sort |
plasma levels of mmp-7 and timp-1 in laboratory diagnostics and differentiation of selected histological types of epithelial ovarian cancers |
publisher |
BMC |
series |
Journal of Ovarian Research |
issn |
1757-2215 |
publishDate |
2017-06-01 |
description |
Abstract Background MMP-7 and TIMP-1 may play a role in the pathogenesis of cancer disease. In this study we investigated plasma levels of selected metalloproteinase and its tissue inhibitor in comparison to plasma levels of the commonly accepted tumor markers (CA 125 and HE4) in selected histological types of epithelial ovarian cancer patients as compared to control groups: patients with a benign ovarian tumor and healthy subjects. Plasma levels of MMP-7 and TIMP-1 were determined using ELISA, CA 125 and HE4 – by CMIA methods. Results Plasma levels of all biomarkers studied were significantly higher in ovarian cancer patients as compared to both control groups. MMP-7 demonstrated comparable to HE4 or CA125 values of diagnostic sensitivity (SE: 61%; 68%; 58%, respectively), specificity (SP: 95%; 95%; 98%, respectively), positive (PPV: 93%; 96%; 98%, respectively) and negative predictive values (NPV: 61%; 66%; 60%, respectively) in the groups tested. The combined use of the aforementioned biomarkers resulted in a further increase in diagnostic criteria and AUC, especially in the early stages of the disease. Conclusions These findings suggest the usefulness of combining MMP-7 with CA 125 and HE4 in the diagnosis of epithelial ovarian cancer as a new tumor marker panel. |
topic |
MMP-7 TIMP-1 HE4 CA125 Epithelial ovarian cancer Tumor markers |
url |
http://link.springer.com/article/10.1186/s13048-017-0338-z |
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