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Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines

One of the main obstacles to the effective treatment of ovarian cancer patients continues to be the drug resistance of cancer cells. Osteoblast-Specific Factor 2 (OSF-2, Periostin) is a secreted extracellular matrix protein (ECM) expressed in fibroblasts during bone and teeth development. Expression...

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Autores principales: Sterzyńska, Karolina, Kaźmierczak, Dominika, Klejewski, Andrzej, Świerczewska, Monika, Wojtowicz, Karolina, Nowacka, Marta, Brązert, Jacek, Nowicki, Michał, Januchowski, Radosław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719218/
https://www.ncbi.nlm.nih.gov/pubmed/31412536
http://dx.doi.org/10.3390/ijms20163927
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author Sterzyńska, Karolina
Kaźmierczak, Dominika
Klejewski, Andrzej
Świerczewska, Monika
Wojtowicz, Karolina
Nowacka, Marta
Brązert, Jacek
Nowicki, Michał
Januchowski, Radosław
author_facet Sterzyńska, Karolina
Kaźmierczak, Dominika
Klejewski, Andrzej
Świerczewska, Monika
Wojtowicz, Karolina
Nowacka, Marta
Brązert, Jacek
Nowicki, Michał
Januchowski, Radosław
author_sort Sterzyńska, Karolina
collection PubMed
description One of the main obstacles to the effective treatment of ovarian cancer patients continues to be the drug resistance of cancer cells. Osteoblast-Specific Factor 2 (OSF-2, Periostin) is a secreted extracellular matrix protein (ECM) expressed in fibroblasts during bone and teeth development. Expression of OSF-2 has been also related to the progression and drug resistance of different tumors. The present study investigated the role of OSF-2 by evaluating its expression in the primary serous ovarian cancer cell line, sensitive (W1) and resistant to doxorubicin (DOX) (W1DR) and methotrexate (MTX) (W1MR). The OSF-2 transcript (real-time PCR analysis), protein expression in cell lysates and cell culture medium (western blot), and expression of the OSF-2 protein in cell lines (immunofluorescence) were investigated in this study. Increased expression of OSF-2 mRNA was observed in drug-resistant cells and followed by increased protein expression in cell culture media of drug-resistant cell lines. A subpopulation of ALDH1A1-positive cells was noted for W1DR and W1MR cell lines; however, no direct co-expression with OSF-2 was demonstrated. Both drugs induced OSF-2 expression after a short period of exposure of the drug-sensitive cell line to DOX and MTX. The obtained results indicate that OSF-2 expression might be associated with the development of DOX and MTX resistance in the primary serous W1 ovarian cancer cell line.
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spelling pubmed-67192182019-09-10 Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines Sterzyńska, Karolina Kaźmierczak, Dominika Klejewski, Andrzej Świerczewska, Monika Wojtowicz, Karolina Nowacka, Marta Brązert, Jacek Nowicki, Michał Januchowski, Radosław Int J Mol Sci Article One of the main obstacles to the effective treatment of ovarian cancer patients continues to be the drug resistance of cancer cells. Osteoblast-Specific Factor 2 (OSF-2, Periostin) is a secreted extracellular matrix protein (ECM) expressed in fibroblasts during bone and teeth development. Expression of OSF-2 has been also related to the progression and drug resistance of different tumors. The present study investigated the role of OSF-2 by evaluating its expression in the primary serous ovarian cancer cell line, sensitive (W1) and resistant to doxorubicin (DOX) (W1DR) and methotrexate (MTX) (W1MR). The OSF-2 transcript (real-time PCR analysis), protein expression in cell lysates and cell culture medium (western blot), and expression of the OSF-2 protein in cell lines (immunofluorescence) were investigated in this study. Increased expression of OSF-2 mRNA was observed in drug-resistant cells and followed by increased protein expression in cell culture media of drug-resistant cell lines. A subpopulation of ALDH1A1-positive cells was noted for W1DR and W1MR cell lines; however, no direct co-expression with OSF-2 was demonstrated. Both drugs induced OSF-2 expression after a short period of exposure of the drug-sensitive cell line to DOX and MTX. The obtained results indicate that OSF-2 expression might be associated with the development of DOX and MTX resistance in the primary serous W1 ovarian cancer cell line. MDPI 2019-08-13 /pmc/articles/PMC6719218/ /pubmed/31412536 http://dx.doi.org/10.3390/ijms20163927 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sterzyńska, Karolina
Kaźmierczak, Dominika
Klejewski, Andrzej
Świerczewska, Monika
Wojtowicz, Karolina
Nowacka, Marta
Brązert, Jacek
Nowicki, Michał
Januchowski, Radosław
Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title_full Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title_fullStr Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title_full_unstemmed Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title_short Expression of Osteoblast-Specific Factor 2 (OSF-2, Periostin) Is Associated with Drug Resistance in Ovarian Cancer Cell Lines
title_sort expression of osteoblast-specific factor 2 (osf-2, periostin) is associated with drug resistance in ovarian cancer cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719218/
https://www.ncbi.nlm.nih.gov/pubmed/31412536
http://dx.doi.org/10.3390/ijms20163927
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