Li Xin, Fan Shengjun, Pan Xueyang, Xiaokaiti Yilixiati, Duan Jianhui, Shi Yundi, Pan Yan, Tie Lu, Wang Xin, Li Yuhua, Li Xuejun
State Key Laboratory of Natural and Biomimetic Drugs, Department of Pharmacology, School of Basic Medical Sciences, Peking University and Beijing Key Laboratory of Tumor Systems Biology, Peking University, Beijing 100191, China.
Current address: University of Minnesota, Twin cities, MN 55455, USA.
Oncotarget. 2016 Dec 27;7(52):86225-86238. doi: 10.18632/oncotarget.13368.
Tumor metastasis is a major cause leading to the deaths of cancer patients. Nordihydroguaiaretic acid (NDGA) is a natural product that has been demonstrated to show therapeutic values in multiple diseases. In this study, we report that NDGA can inhibit cell migration and tumor metastasis via a novel mechanism. NDGA suppresses NRP1 function by downregulating its expression, which leads to attenuated cell motility, cell adhesion to ECM and FAK signaling in cancer cells. Moreover, due to its cross-cell type activity on NRP1 suppression, NDGA also impairs angiogenesis function of endothelial cells and fibronectin assembly by fibroblasts, both of which are critical to promote metastasis. Based on these comprehensive effects, NDGA effectively suppresses tumor metastasis in nude mice model. Our findings reveal a novel mechanism underlying the anti-metastasis function of NDGA and indicate the potential value of NDGA in NRP1 targeting therapy for selected subtypes of cancer.
肿瘤转移是导致癌症患者死亡的主要原因。去甲二氢愈创木酸(NDGA)是一种天然产物,已被证明在多种疾病中具有治疗价值。在本研究中,我们报告NDGA可通过一种新机制抑制细胞迁移和肿瘤转移。NDGA通过下调NRP1的表达来抑制其功能,这导致癌细胞的细胞运动性减弱、细胞与细胞外基质的粘附以及FAK信号传导减弱。此外,由于其对NRP1抑制的跨细胞类型活性,NDGA还损害内皮细胞的血管生成功能和成纤维细胞的纤连蛋白组装,这两者对促进转移都至关重要。基于这些综合作用,NDGA在裸鼠模型中有效抑制肿瘤转移。我们的研究结果揭示了NDGA抗转移功能的新机制,并表明NDGA在针对特定癌症亚型的NRP1靶向治疗中的潜在价值。