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Article

Establishment and Characterization of the Novel High-Grade Serous Ovarian Cancer Cell Line OVPA8

by
Patrycja Tudrej
1,
Magdalena Olbryt
1,
Ewa Zembala-Nożyńska
2,
Katarzyna A. Kujawa
1,
Alexander J. Cortez
1,
Anna Fiszer-Kierzkowska
3,
Wojciech Pigłowski
3,
Barbara Nikiel
2,
Magdalena Głowala-Kosińska
4,
Aleksandra Bartkowska-Chrobok
5,
Andrzej Smagur
4,
Wojciech Fidyk
4 and
Katarzyna M. Lisowska
1,*
1
Center for Translational Research and Molecular Biology of Cancer, Maria Skłodowskaj-Curie Institute—Oncology Center, Gliwice Branch, ul. Wybrzeże Armii Krajowej 15, 44-101 Gliwice, Poland
2
Thumor Pathology Department, Maria Skłodowskaj-Curie Institute—Oncology Center, Gliwice Branch, ul. Wybrzeże Armii Krajowej 15, 44-101 Gliwice, Poland
3
Molecular Diagnostics Laboratory, Maria Skłodowskaj-Curie Institute—Oncology Center, Gliwice Branch, ul. Wybrzeże Armii Krajowej 15, 44-101 Gliwice, Poland
4
Department of Bone Marrow Transplantation and Hematology-Oncology, Maria Skłodowskaj-Curie Institute—Oncology Center, Gliwice Branch, ul. Wybrzeże Armii Krajowej 15, 44-101 Gliwice, Poland
5
Department of Hematology and Bone Marrow Transplantation, Andrzej Mielęcki Independent Public Hospital, ul. Dąbrowskiego 25, 40-032 Katowice, Poland
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(7), 2080; https://doi.org/10.3390/ijms19072080
Submission received: 6 June 2018 / Revised: 10 July 2018 / Accepted: 13 July 2018 / Published: 17 July 2018
(This article belongs to the Special Issue Ovarian Cancer: Pathogenesis, Diagnosis, and Treatment)
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Abstract

High-grade serous ovarian carcinoma (HGSOC) is the most frequent histological type of ovarian cancer and the one with worst prognosis. Unfortunately, the majority of established ovarian cancer cell lines which are used in the research have unclear histological origin and probably do not represent HGSOC. Thus, new and reliable models of HGSOC are needed. Ascitic fluid from a patient with recurrent HGSOC was used to establish a stable cancer cell line. Cells were characterized by cytogenetic karyotyping and short tandem repeat (STR) profiling. New generation sequencing was applied to test for hot-spot mutations in 50 cancer-associated genes and fluorescence in situ hybridization (FISH) analysis was used to check for TP53 status. Cells were analyzed for expression of several marker genes/proteins by reverse-transcription polymerase chain reaction (RT-PCR), fluorescence-activated cell sorting (FACS), and immunocytochemistry (ICC). Functional tests were performed to compare OVPA8 cells with five commercially available and frequently used ovarian cancer cell lines: SKOV3, A2780, OVCAR3, ES2, and OAW42. Our newly-established OVPA8 cell line shows morphologic and genetic features consistent with HGSOC, such as epithelial morphology, multiple chromosomal aberrations, TP53 mutation, BRCA1 mutation, and loss of one copy of BRCA2. The OVPA8 line has a stable STR profile. Cells are positive for EpCAM, CK19, and CD44; they have relatively low plating efficiency/ability to form spheroids, a low migration rate, and intermediate invasiveness in matrigel, as compared to other ovarian cancer lines. OVPA8 is sensitive to paclitaxel and resistant to cisplatin. We also tested two FGFR inhibitors; OVPA8 cells were resistant to AZD4547 (AstraZeneca, London, UK), but sensitive to the new inhibitor CPL304-110-01 (Celon Pharma, Łomianki/Kiełpin, Poland). We have established and characterized a novel cell line, OVPA8, which can be a valuable preclinical model for studies on high-grade serous ovarian cancer.
Keywords: high-grade serous ovarian cancer; cell line; fibroblast growth factor inhibitor CPL304-110-01 high-grade serous ovarian cancer; cell line; fibroblast growth factor inhibitor CPL304-110-01
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MDPI and ACS Style

Tudrej, P.; Olbryt, M.; Zembala-Nożyńska, E.; Kujawa, K.A.; Cortez, A.J.; Fiszer-Kierzkowska, A.; Pigłowski, W.; Nikiel, B.; Głowala-Kosińska, M.; Bartkowska-Chrobok, A.; et al. Establishment and Characterization of the Novel High-Grade Serous Ovarian Cancer Cell Line OVPA8. Int. J. Mol. Sci. 2018, 19, 2080. https://doi.org/10.3390/ijms19072080

AMA Style

Tudrej P, Olbryt M, Zembala-Nożyńska E, Kujawa KA, Cortez AJ, Fiszer-Kierzkowska A, Pigłowski W, Nikiel B, Głowala-Kosińska M, Bartkowska-Chrobok A, et al. Establishment and Characterization of the Novel High-Grade Serous Ovarian Cancer Cell Line OVPA8. International Journal of Molecular Sciences. 2018; 19(7):2080. https://doi.org/10.3390/ijms19072080

Chicago/Turabian Style

Tudrej, Patrycja, Magdalena Olbryt, Ewa Zembala-Nożyńska, Katarzyna A. Kujawa, Alexander J. Cortez, Anna Fiszer-Kierzkowska, Wojciech Pigłowski, Barbara Nikiel, Magdalena Głowala-Kosińska, Aleksandra Bartkowska-Chrobok, and et al. 2018. "Establishment and Characterization of the Novel High-Grade Serous Ovarian Cancer Cell Line OVPA8" International Journal of Molecular Sciences 19, no. 7: 2080. https://doi.org/10.3390/ijms19072080

APA Style

Tudrej, P., Olbryt, M., Zembala-Nożyńska, E., Kujawa, K. A., Cortez, A. J., Fiszer-Kierzkowska, A., Pigłowski, W., Nikiel, B., Głowala-Kosińska, M., Bartkowska-Chrobok, A., Smagur, A., Fidyk, W., & Lisowska, K. M. (2018). Establishment and Characterization of the Novel High-Grade Serous Ovarian Cancer Cell Line OVPA8. International Journal of Molecular Sciences, 19(7), 2080. https://doi.org/10.3390/ijms19072080

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