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Ovarian cancer has the highest incidence of any malignancy of the female reproductive system and also ranks first for mortality out of all gynecological tumors (1,2). Accounting for 4.3% of female cancer deaths each year, the disease poses a serious threat to women’s lives. At present, surgical resection plus adjuvant chemotherapy is still the preferred treatment method for ovarian cancer. However, the 5-year survival rate and high rates of recurrence and metastasis still present problems for patients after treatment (3). Therefore, there is an urgent need for new diagnostic and therapeutic targets for ovarian cancer to be identified. Original Article

translational cancer research

microRNA-132 inhibits the proliferation, migration, and invasion of ovarian cancer cells by regulating CT10 oncogenic gene homolog II-related signaling pathways