OxLDL promotes lymphangiogenesis and lymphatic metastasis in gastric cancer by upregulating VEGF‑C expression and secretion

Caiqi Ma(Sun Yat-sen University), Jinye Xie(Sun Yat-sen University), Chuanghua Luo(Sun Yat-sen University), Haofan Yin(Sun Yat-sen University), Ruopu Li(Sun Yat-sen University), Xi Wang(Sun Yat-sen University), Wenjun Xiong(Guangdong Provincial Hospital of Traditional Chinese Medicine), Ting Zhang(South China University of Technology), Ping Jiang(Sun Yat-sen University), Weiwei Qi(Sun Yat-sen University), Ti Zhou(Sun Yat-sen University), Zhonghan Yang(Sun Yat-sen University), Wei Wang(Guangdong Provincial Hospital of Traditional Chinese Medicine), Jian‐xing Ma(University of Oklahoma Health Sciences Center), Guoquan Gao(Sun Yat-sen University), Xia Yang(Sun Yat-sen University)
International Journal of Oncology
November 26, 2018
Cited by 41Open Access
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Abstract

Gastric cancer is one of the most malignant tumor types, and its metastasis is a notable cause of mortality. Among the methods of tumor metastasis, lymphatic metastasis is the predominant one in gastric cancer. A previous study reported that the plasma oxidized low‑density lipoprotein (oxLDL) is the risk factor associated with the development of tumors in patients with abnormal lipid metabolism, but the influence of plasma oxLDL in the lymphatic metastasis of gastric cancer remains unclear. In the present study, the concentration of plasma oxLDL from patients with gastric cancer was detected with an ELISA kit, and the lymphatic vessel density in gastric cancer tissues was determined by D2‑40 staining. The correlation analysis of oxLDL concentration and lymphatic vessel density demonstrated that plasma oxLDL was positively correlated with lymphatic metastasis in patients with gastric cancer. Subsequently, the popliteal lymph node metastasis animal experiment with nude mice confirmed that oxLDL could promote the lymphatic metastasis of gastric cancer. Following this, the western blotting and ELISA data demonstrated that oxLDL promoted the expression and secretion of vascular endothelia growth factor (VEGF)‑C in gastric cancer cell lines. Finally, blocking the lectin‑like oxLDL‑1 (LOX‑1) receptor, a specific receptor for oxLDL, and the nuclear factor (NF)‑κB signaling pathway following oxLDL (50 µg/ml) treatment in HGC‑27 cells revealed that oxLDL could activate the NF‑κB signaling pathway mediated by LOX‑1, with subsequent upregulation of VEGF‑C expression, and secretion in and from gastric cancer cells, and finally that it could promote the lymphatic metastasis of gastric cancer. These data indicate the association between the plasma oxLDL and the lymphatic metastasis of gastric cancer, and indicate that oxLDL elimination may be a potential therapeutic target for the prevention and intervention of early lymph node metastasis in gastric cancer.


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