Establishment and characterization of a novel ovarian clear cell carcinoma cell line, TU-OC-2, with loss of ARID1A expression.

Abstract

A new cell line of human ovarian clear cell carcinoma (CCC), TU-OC-2, was established and characterized. The cells were polygonal in shape, grew in monolayers without contact inhibition and were arranged in islands like pieces of a jigsaw puzzle. The chromosome numbers ranged from 41 to 96. A low rate of proliferation was observed and the doubling time was 37.5 h. The IC50 values of cisplatin, 7-ethyl-10-hydroxycamptothecin (SN38), which is an active metabolite of camptothecin, and paclitaxel were 7.7 μM, 17.7 nM and 301 nM, respectively. The drug sensitivity assay indicated that TU-OC-2 was sensitive to SN38, but resistant to cisplatin and paclitaxel. Mutational analysis revealed that TU-OC-2 cells have no mutations of PIK3CA in exons 9 and 20 and of TP53 in exons 4-9. We observed the loss of ARID1A protein expression in TU-OC-2 cells by western blot analysis and in the original tumor tissue by immunohistochemistry. This cell line may be useful for studying the chemoresistant mechanisms of CCC and exploring novel therapeutic targets such as the ARID1A-related signaling pathway.

• Authors: Seiya Sato, Hiroaki Itamochi, Nao Oumi, Youhei Chiba, Tetsuro Oishi, Muneaki Shimada, Shinya Sato, Jun Chikumi, Michiko Nonaka, Akiko Kudoh, Hiroaki Komatsu, Tasuku Harada, Toru Sugiyama
• Journal: Human cell (Hum Cell) Vol. 29 Issue 4 Pg. 181-7 (Oct 2016) ISSN: 1749-0774 [Electronic] Japan
• PMID: 26960408 (Publication Type: Journal Article)

Chemical References

• ARID1A protein, human
• Antineoplastic Agents
• DNA-Binding Proteins
• Nuclear Proteins
• Transcription Factors
• Irinotecan
• Paclitaxel
• Cisplatin
• Camptothecin

Topics

• Adenocarcinoma, Clear Cell (genetics, pathology)
• Antineoplastic Agents (pharmacology)
• Camptothecin (analogs & derivatives, pharmacology)
• Cell Line, Tumor
• Chromosomes
• Cisplatin (pharmacology)
• DNA-Binding Proteins
• Drug Resistance, Neoplasm
• Female
• Gene Deletion
• Gene Expression
• Humans
• Irinotecan
• Nuclear Proteins (genetics)
• Ovarian Neoplasms (genetics, pathology)
• Paclitaxel (pharmacology)
• Signal Transduction (genetics, physiology)
• Transcription Factors (genetics)