Combined Usage of MDK Inhibitor Augments Interferon-γ Anti-Tumor Activity in the SKOV3 Human Ovarian Cancer Cell Line

被引:5
作者
Liu, Qun [1 ,2 ]
Tan, Jingyu [3 ]
Zhao, Zhenguo [4 ]
Li, Ruijun [3 ]
Zheng, Luyu [3 ]
Chen, Xiangyu [3 ]
Li, Lina [3 ]
Dong, Xichen [3 ]
Wen, Tao [3 ]
Liu, Jian [3 ,5 ]
机构
[1] Capital Med Univ, Beijing Anzhen Hosp, Dept Gynaecol & Obstet, Beijing 100029, Peoples R China
[2] Capital Med Univ, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Dept Gynecol Oncol, Beijing 100006, Peoples R China
[3] Capital Med Univ, Beijing Chao Yang Hosp, Med Res Ctr, Beijing 100020, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Canc Ctr, Dept Orthopaed,Natl Clin Res Ctr Canc, Beijing 100021, Peoples R China
[5] Capital Med Univ, Beijing Chao Yang Hosp, Dept Oncol, Beijing 100020, Peoples R China
基金
中国国家自然科学基金;
关键词
ovarian cancer; interferon-gamma; therapeutic efficacy; MDK inhibitor; combined utilization; IFN-GAMMA; MESENCHYMAL TRANSITION; 1ST-LINE TREATMENT; ENHANCEMENT; PROGRESSION; APOPTOSIS;
D O I
10.3390/biomedicines11010008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian cancer (OC) is a particularly lethal disease due to intratumoral heterogeneity, resistance to traditional chemotherapy, and poor response to targeted therapy and immunotherapy. Interferon-gamma (IFN-gamma) is an attractive therapeutic cytokine, with positive responses achieved in multiple OC clinical trials. However, clinical application of IFN-gamma in OC is still hindered, due to the severe toxicity when used at higher levels, as well as the considerable pro-metastatic adverse effect when used at lower levels. Thus, an effective combined intervention is needed to enhance the anti-tumor efficacy of IFN-gamma and to suppress the IFN-gamma-induced metastasis. Here, we uncovered that OC cells develop an adaptive strategy by upregulating midkine (MDK) to counteract the IFN-gamma-induced anti-tumor activity and to fuel IFN-gamma-induced metastasis. We showed that MDK is a critical downstream target of IFN-gamma in OC, and that this regulation acts in a dose-dependent manner and is mediated by STAT1. Gain-of-function studies showed that MDK overexpression promotes cell proliferation and metastasis in OC, indicating that IFN-gamma-activated MDK may antagonize IFN-gamma in inhibiting OC proliferation but synergize IFN-gamma in promoting OC metastasis. Subsequently, we assessed the influence of MDK inhibition on IFN-gamma-induced anti-proliferation and pro-metastasis effects using an MDK inhibitor (iMDK), and we found that MDK inhibition robustly enhanced IFN-gamma-induced growth inhibition (all CIs < 0.1) and reversed IFN-gamma-driven epithelial-to-mesenchymal transition (EMT) and metastasis in OC in vitro. Collectively, these data identify an IFN-gamma responsive protein, MDK, in counteracting anti-proliferation while endowing the pro-metastatic role of IFN-gamma in cancer treatment, and we therefore propose the combined utilization of the MDK inhibitor in IFN-gamma-based therapies in future OC treatment.
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页数:13
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