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EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo
BACKGROUND: EGF-containing fibulin-like extracellular matrix protein 2 (EFEMP2) is an extracellular matrix (ECM) glycoprotein, which is regarded as potential prognostic biomarkers in some carcinoma. Little is known about the association of EFEMP2 and breast cancer. METHODS: EFEMP2 expressions in nor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826198/ https://www.ncbi.nlm.nih.gov/pubmed/31802903 http://dx.doi.org/10.2147/OTT.S221219 |
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author | Kang, Ning Zhou, Jijun Xu, Jia Zhou, Dongsheng Shi, Weichen |
author_facet | Kang, Ning Zhou, Jijun Xu, Jia Zhou, Dongsheng Shi, Weichen |
author_sort | Kang, Ning |
collection | PubMed |
description | BACKGROUND: EGF-containing fibulin-like extracellular matrix protein 2 (EFEMP2) is an extracellular matrix (ECM) glycoprotein, which is regarded as potential prognostic biomarkers in some carcinoma. Little is known about the association of EFEMP2 and breast cancer. METHODS: EFEMP2 expressions in normal breast tissue, benign fibroadenoma, breast cancer, the normal mammary epithelial cell line, and 4 different invasive breast cancer cell lines were evaluated by immunohistochemistry (IHC) or immunocytochemistry (ICC) and real time quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR). Expression and prognostic value of EFEMP2 in breast cancer were verified by the Public databases (Oncomine and Kaplan-Meier plotter database). Lentiviral vector with EFEMP2 cDNA was constructed and used to infect breast cancer cell lines to investigate the effects of EFEMP2 on the biological behavior of breast cancer cells by functional in vitro and in vivo assays. RESULTS: Down-regulated EFEMP2 expression was found in breast cancer tissues and cells, and low expression of EFEMP2 was associated with poor prognosis in patients with breast cancer. Analysis by the Public database leaded to the same conclusion. Up-regulated EFEMP2 expression significantly hampered the invasion and metastasis abilities of breast cancer cells and the process of epithelial interstitial transformation (EMT) via the Wnt/β-catenin pathway. CONCLUSION: EFEMP2 expression was lower in breast cancer and closely related to the prognosis of patients, its anti-oncogenic roles indicated the underlying therapeutic target for the future treatment of breast cancer. |
format | Online Article Text |
id | pubmed-6826198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68261982019-12-04 EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo Kang, Ning Zhou, Jijun Xu, Jia Zhou, Dongsheng Shi, Weichen Onco Targets Ther Original Research BACKGROUND: EGF-containing fibulin-like extracellular matrix protein 2 (EFEMP2) is an extracellular matrix (ECM) glycoprotein, which is regarded as potential prognostic biomarkers in some carcinoma. Little is known about the association of EFEMP2 and breast cancer. METHODS: EFEMP2 expressions in normal breast tissue, benign fibroadenoma, breast cancer, the normal mammary epithelial cell line, and 4 different invasive breast cancer cell lines were evaluated by immunohistochemistry (IHC) or immunocytochemistry (ICC) and real time quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR). Expression and prognostic value of EFEMP2 in breast cancer were verified by the Public databases (Oncomine and Kaplan-Meier plotter database). Lentiviral vector with EFEMP2 cDNA was constructed and used to infect breast cancer cell lines to investigate the effects of EFEMP2 on the biological behavior of breast cancer cells by functional in vitro and in vivo assays. RESULTS: Down-regulated EFEMP2 expression was found in breast cancer tissues and cells, and low expression of EFEMP2 was associated with poor prognosis in patients with breast cancer. Analysis by the Public database leaded to the same conclusion. Up-regulated EFEMP2 expression significantly hampered the invasion and metastasis abilities of breast cancer cells and the process of epithelial interstitial transformation (EMT) via the Wnt/β-catenin pathway. CONCLUSION: EFEMP2 expression was lower in breast cancer and closely related to the prognosis of patients, its anti-oncogenic roles indicated the underlying therapeutic target for the future treatment of breast cancer. Dove 2019-10-30 /pmc/articles/PMC6826198/ /pubmed/31802903 http://dx.doi.org/10.2147/OTT.S221219 Text en © 2019 Kang 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 Kang, Ning Zhou, Jijun Xu, Jia Zhou, Dongsheng Shi, Weichen EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title | EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title_full | EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title_fullStr | EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title_full_unstemmed | EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title_short | EFEMP2 Inhibits Breast Cancer Invasion And Metastasis In Vitro And In Vivo |
title_sort | efemp2 inhibits breast cancer invasion and metastasis in vitro and in vivo |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826198/ https://www.ncbi.nlm.nih.gov/pubmed/31802903 http://dx.doi.org/10.2147/OTT.S221219 |
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