Author:
Tian Liming,Li Xuemei,Lai Huiling,Sun Tingting,Li Xiaohui,Wu Linxiang,Wu Chuling,Yao Shuzhong,Ren Yufeng,He Shasha,Yang Guofen
Abstract
AbstractOvarian cancer has the highest mortality rate among gynecologic tumors, with a 5-year survival rate of less than 25%. There is an urgent need for early diagnosis and new drugs to reduce the disease burden of ovarian cancer. The aim of this study was to investigate the effectiveness of SLC11A2 as a therapeutic target and marker for ovarian cancer. Expression data of SLC11A2 were obtained from public databases. Then, the biological functions of SLC11A2 were validated in four ovarian cancer cell lines. Finally, we collected ovarian cancer clinical tissues, serum, and plasma exosomes and used immunohistochemistry, Elisa, and liquid chromatography-mass spectrometry (LC–MS) to validate the test efficacy of SLC11A2. The results showed that ovarian cancers with high SLC11A2 mRNA expression had shorter 5-year PFS and MST. Knockdown of SLC11A2 reduced ovarian cancer migration and increased cisplatin-induced apoptosis. Serum SLC11A2 may help improve the detection rate of ovarian cancer.
Funder
National Natural Science Foundation of China
the National Key R&D Program of China
Natural Science Foundation of Guangdong Province
Publisher
Springer Science and Business Media LLC