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Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer

BACKGROUND: The biological and clinical significance of matrix metalloproteinase-7 (MMP-7) in cervical cancer remains unknown. Here, we investigated the function of MMP-7 in cervical cancer cells and evaluated its clinical significance in both tissues and serum from cervical cancer patients. METHODS...

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Autores principales: Zhu, Linyan, Zheng, Xiaojiao, Du, Yongming, Xing, Yan, Xu, Kejun, Cui, Lining
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055895/
https://www.ncbi.nlm.nih.gov/pubmed/30050312
http://dx.doi.org/10.2147/OTT.S160998
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author Zhu, Linyan
Zheng, Xiaojiao
Du, Yongming
Xing, Yan
Xu, Kejun
Cui, Lining
author_facet Zhu, Linyan
Zheng, Xiaojiao
Du, Yongming
Xing, Yan
Xu, Kejun
Cui, Lining
author_sort Zhu, Linyan
collection PubMed
description BACKGROUND: The biological and clinical significance of matrix metalloproteinase-7 (MMP-7) in cervical cancer remains unknown. Here, we investigated the function of MMP-7 in cervical cancer cells and evaluated its clinical significance in both tissues and serum from cervical cancer patients. METHODS: First, we analyzed the expression of MMP-7 in cervical cancer using Oncomine microarray data and examined its expression in cervical tissues by quantitative real-time polymerase chain reaction and Western blotting. Second, we utilized gene silencing to explore the role of MMP-7 in cells. Finally, we examined the MMP-7 levels in patients with cervical cancer and normal serum by enzyme-linked immunosorbent assay. Moreover, we further investigated the relationship between MMP-7 expression and pathological features. RESULTS: The mRNA and protein MMP-7 levels were higher in cervical cancer tissues than in healthy controls. Silencing of MMP-7 significantly decreased cervical cancer cell proliferation, migration, and invasion. The serum MMP-7 levels were significantly higher in cervical cancer patients than in healthy subjects (P<0.01). Further, higher MMP-7 expression was associated with increased lymph metastasis (P=0.021), pathological grade (P=0.039, P=0.047), and clinical stage (P=0.049, P=0.046). CONCLUSION: MMP-7 appears to act as an oncogene in cervical cancer cells and is involved in cell proliferation, migration, and invasion. MMP-7 expression was significantly higher in the tissue and serum of cervical cancer patients compared to healthy individuals and was correlated with increased pathalogical grade, clinical stage, and lymph metastasis. Therefore, our data provide novel evidence that MMP-7 may be a clinically relevant biomarker for cervical cancer.
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spelling pubmed-60558952018-07-26 Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer Zhu, Linyan Zheng, Xiaojiao Du, Yongming Xing, Yan Xu, Kejun Cui, Lining Onco Targets Ther Original Research BACKGROUND: The biological and clinical significance of matrix metalloproteinase-7 (MMP-7) in cervical cancer remains unknown. Here, we investigated the function of MMP-7 in cervical cancer cells and evaluated its clinical significance in both tissues and serum from cervical cancer patients. METHODS: First, we analyzed the expression of MMP-7 in cervical cancer using Oncomine microarray data and examined its expression in cervical tissues by quantitative real-time polymerase chain reaction and Western blotting. Second, we utilized gene silencing to explore the role of MMP-7 in cells. Finally, we examined the MMP-7 levels in patients with cervical cancer and normal serum by enzyme-linked immunosorbent assay. Moreover, we further investigated the relationship between MMP-7 expression and pathological features. RESULTS: The mRNA and protein MMP-7 levels were higher in cervical cancer tissues than in healthy controls. Silencing of MMP-7 significantly decreased cervical cancer cell proliferation, migration, and invasion. The serum MMP-7 levels were significantly higher in cervical cancer patients than in healthy subjects (P<0.01). Further, higher MMP-7 expression was associated with increased lymph metastasis (P=0.021), pathological grade (P=0.039, P=0.047), and clinical stage (P=0.049, P=0.046). CONCLUSION: MMP-7 appears to act as an oncogene in cervical cancer cells and is involved in cell proliferation, migration, and invasion. MMP-7 expression was significantly higher in the tissue and serum of cervical cancer patients compared to healthy individuals and was correlated with increased pathalogical grade, clinical stage, and lymph metastasis. Therefore, our data provide novel evidence that MMP-7 may be a clinically relevant biomarker for cervical cancer. Dove Medical Press 2018-07-20 /pmc/articles/PMC6055895/ /pubmed/30050312 http://dx.doi.org/10.2147/OTT.S160998 Text en © 2018 Zhu et al. 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.
spellingShingle Original Research
Zhu, Linyan
Zheng, Xiaojiao
Du, Yongming
Xing, Yan
Xu, Kejun
Cui, Lining
Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title_full Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title_fullStr Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title_full_unstemmed Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title_short Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
title_sort matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055895/
https://www.ncbi.nlm.nih.gov/pubmed/30050312
http://dx.doi.org/10.2147/OTT.S160998
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