| Literature DB >> 33420363 |
Kosuke Yoshida1,2,3, Akira Yokoi4,5, Mai Sugiyama6, Shingo Oda3, Kazuhisa Kitami1, Satoshi Tamauchi1, Yoshiki Ikeda1, Nobuhisa Yoshikawa1, Kimihiro Nishino1, Kaoru Niimi1, Shiro Suzuki1, Fumitaka Kikkawa1, Tsuyoshi Yokoi3, Hiroaki Kajiyama1.
Abstract
Ovarian clear cell carcinoma (OCCC) is a histological subtype of epithelial ovarian cancer and exhibits dismal prognosis due to chemoresistance. Moreover, only few effective therapeutic options exist for patients with recurrent OCCC, and an understanding of its molecular characteristics is essential for the development of novel therapeutic approaches. In the present study, we investigated unique MicroRNAs (miRNA) profiles in recurrent/metastatic OCCC and the role of miRNAs in cisplatin resistance. Comprehensive miRNA sequencing revealed that expression of several miRNAs, including miR-508-3p, miR-509-3p, miR-509-3-5p, and miR-514a-3p was remarkably less in recurrent cancer tissues when compared with that in paired primary cancer tissues. These miRNAs are located in the chrXq27.3 region on the genome. Moreover, its expression was negative in omental metastases in two patients with advanced OCCC. In vitro analyses revealed that overexpression of miR-509-3p and miR-509-3-5p reversed cisplatin resistance and yes-associated protein 1 (YAP1) was partially responsible for the resistance. Immunohistochemistry revealed that YAP1 expression was inversely correlated with the chrXq27.3 miRNA cluster expression. In conclusion, these findings suggest that alteration of the chrXq27.3 miRNA cluster could play a critical role in chemoresistance and miRNAs in the cluster and their target genes can be potential therapeutic targets.Entities:
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Year: 2021 PMID: 33420363 PMCID: PMC7892337 DOI: 10.1038/s41388-020-01595-3
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867