| Literature DB >> 30129654 |
Chengjuan Jin1,2, Zhaojian Liu3, Yingwei Li1, Hualei Bu1, Yu Wang1, Ying Xu1, Chunping Qiu1, Shi Yan1, Cunzhong Yuan1, Rongrong Li1, Nannan Diao4, Zhiwei Zhang1, Xiangxiang Wang1, Lidong Liu1, Beihua Kong1.
Abstract
Activation of the FOXM1 signaling pathway and the PI3K/AKT/mTOR signaling pathway is associated with poor prognosis in ovarian cancer. In this study, we demonstrated that P15PAF (KIAA0101) was significantly upregulated in high-grade serous ovarian cancer (HGSOC) and that high KIAA0101 expression was associated with poor prognosis. FOXM1 transcriptionally activated KIAA0101 to drive proliferation and metastasis of ovarian cancer cells. KIAA0101 activated the PI3K/AKT/mTOR signaling pathway to inhibit cisplatin-induced apoptosis and autophagy in ovarian cancer cells resulting in cisplatin resistance. Thus, KIAA0101 was closely related to the FOXM1 and PI3K/AKT/mTOR signaling pathways. Collectively, these findings provide insights into the mechanisms of poor prognosis of ovarian cancer and have implications for the development of both predictive and therapeutic biomarkers for the treatment of ovarian cancer.Entities:
Keywords: FOXM1; HGSOC; P15PAF; PI3K/AKT/mTOR
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Year: 2018 PMID: 30129654 DOI: 10.1002/ijc.31800
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396