Lin Chih-Yang, Wang Shih-Wei, Guo Jeng-Hung, Tai Huai-Ching, Sun Wen-Chun, Lai Cheng-Ta, Yang Chen-Yu, Liu Shih-Chia, Fong Yi-Chin, Tang Chih-Hsin
Department of Pharmacology, School of Medicine, China Medical University, Taichung 404022, Taiwan.
Institute of Biomedical Sciences, Mackay Medical College, Taipei 104217, Taiwan.
Biomedicines. 2021 Sep 27;9(10):1330. doi: 10.3390/biomedicines9101330.
Chondrosarcoma is a malignant bone tumor with high metastatic potential. Lymphangiogenesis is a critical biological step in cancer metastasis. WNT1-inducible signaling pathway protein 3 (WISP-3) regulates angiogenesis and facilitates chondrosarcoma metastasis, but the role of WISP-3 in chondrosarcoma lymphangiogenesis is unclear. In this study, incubation of chondrosarcoma cells with WISP-3 increased the production of VEGF-C, an important lymphangiogenic factor. Conditioned medium from WISP-3-treated chondrosarcoma cells significantly enhanced lymphatic endothelial cell tube formation. WISP-3-induced stimulation of VEGF-C-dependent lymphangiogenesis inhibited miR-196a-3p synthesis in the ERK, JNK, and p38 signaling pathways. This evidence suggests that the WISP-3/VEGF-C axis is worth targeting in the treatment of lymphangiogenesis in human chondrosarcoma.
软骨肉瘤是一种具有高转移潜能的恶性骨肿瘤。淋巴管生成是癌症转移中的关键生物学步骤。WNT1诱导信号通路蛋白3(WISP-3)调节血管生成并促进软骨肉瘤转移,但WISP-3在软骨肉瘤淋巴管生成中的作用尚不清楚。在本研究中,用WISP-3孵育软骨肉瘤细胞可增加重要淋巴管生成因子VEGF-C的产生。来自WISP-3处理的软骨肉瘤细胞的条件培养基显著增强了淋巴管内皮细胞管的形成。WISP-3诱导的VEGF-C依赖性淋巴管生成刺激抑制了ERK、JNK和p38信号通路中miR-196a-3p的合成。这一证据表明,WISP-3/VEGF-C轴在治疗人类软骨肉瘤淋巴管生成方面值得作为靶点。