| Literature DB >> 26960408 |
Seiya Sato1, Hiroaki Itamochi2, Nao Oumi3, Youhei Chiba1, Tetsuro Oishi3, Muneaki Shimada3, Shinya Sato3, Jun Chikumi3, Michiko Nonaka3, Akiko Kudoh3, Hiroaki Komatsu3, Tasuku Harada3, Toru Sugiyama1.
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.Entities:
Keywords: ARID1A; Chemosensitivity; Establishment; Molecular-targeted therapy; Ovarian clear cell carcinoma
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Year: 2016 PMID: 26960408 DOI: 10.1007/s13577-016-0138-6
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174