标题:SUSD2 promotes cancer metastasis and confers cisplatin resistance in high grade serous ovarian cancer
作者:Xu, Ying; Miao, Chunying; Jin, Chengjuan; Qiu, Chunping; Li, Yinuo; Sun, Xiaomei; Gao, Min; Lu, Nan; Kong, Beihua
作者机构:[Xu, Ying; Miao, Chunying; Jin, Chengjuan; Qiu, Chunping; Li, Yinuo; Sun, Xiaomei; Gao, Min; Kong, Beihua] Shandong Univ, Qilu Hosp, Dept Obstet & Gyn 更多
通讯作者:Kong, BH;Lu, N
通讯作者地址:[Kong, BH]Shandong Univ, Qilu Hosp, Dept Obstet & Gynecol, 107 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China;[Lu, N]Shandong Univ, Sch Med, In 更多
来源:EXPERIMENTAL CELL RESEARCH
出版年:2018
卷:363
期:2
页码:160-170
DOI:10.1016/j.yexcr.2017.12.029
关键词:Notch3; SUSD2; HGSOC; EMT; Resistance
摘要:The activation of Notch3 is associated with potential progression of ovarian cancer, tumor invasion, metastasis and chemoresistance, which account for poor prognosis of high grade serous ovarian cancer (HGSOC). However, the underlying mechanisms of Notch3 are not yet very clear. Here we show that SUSD2 is one of Notch3-regulating genes and the elevated protein expression of SUSD2 in HGSOC. We also found that its high expression level was significantly correlated with worse overall survival, early recurrence and lymph nodes metastasis. Moreover, overexpression of SUSD2 in ovarian cancer cells promoted epithelial-mesenchymal transition (EMT) and the metastatic capacity of malignant cells. In contrast, silencing SUSD2 in aggressive ovarian cancer cells inhibited these processes both in vitro and in vivo. Mechanistically, we found SUSD2 promoted EMT through regulating the expression of EpCAM and EpCAM silencing reversed SUSD2-induced E-cadherin reduction and cells migration. Further experiments indicated a role of SUSD2 in conferring cisplatin resistance in ovarian cancer probably through enhancing autophagy in vitro. Collectively, these findings shed a new insight into the role of Notch3 downstream gene SUSD2 and provided a new therapeutic target for HGSOC.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041591747&doi=10.1016%2fj.yexcr.2017.12.029&partnerID=40&md5=8b6d59e0d1c52ceeaa6776f8c8654cc0
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