Suzuki Mira, Nagane Masaki, Kato Kazuhiro, Yamauchi Akinori, Shimizu Takuto, Yamashita Hiroko, Aihara Naoyuki, Kamiie Junichi, Kawashima Nagako, Naito Shokichi, Yamashita Tadashi
Laboratory of Biochemistry, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.
Department of Breast Surgery, Hokkaido University Hospital, Sapporo, Japan.
Biochem Biophys Res Commun. 2021 Sep 10;569:10-16. doi: 10.1016/j.bbrc.2021.06.063. Epub 2021 Jun 30.
Cancer cells require oxygen and nutrients for growth, making angiogenesis one of the essential components of tumor growth. Gangliosides, constituting membrane lipid rafts, regulate intracellular signal transduction and are involved in the malignancy of cancer cells. While endothelial cells, as well as cancer cells, express vast amounts of gangliosides, the precise function of endothelial gangliosides in angiogenesis remains unclear. In this study, we focused on gangliosides of vascular endothelial cells and analyzed their functions on tumor angiogenesis. In human breast cancer, GM3 synthase was highly expressed in vascular endothelial cells as well as immune cells. Angiogenesis increased in GM3S-KO mice. In BAEC, RNA interference of GM3S showed increased cellular invasion and oxidative stress tolerance through activation of ERK. In the breast cancer model, GM3-KO mice showed an increase in tumor growth and angiogenesis. These results suggest that the endothelial ganglioside GM3 regulates tumor angiogenesis by suppressing cellular invasion and oxidative stress tolerance in endothelial cells.
癌细胞的生长需要氧气和营养物质,这使得血管生成成为肿瘤生长的重要组成部分之一。神经节苷脂构成膜脂筏,调节细胞内信号转导,并参与癌细胞的恶性转化。虽然内皮细胞和癌细胞都表达大量的神经节苷脂,但内皮神经节苷脂在血管生成中的精确功能仍不清楚。在本研究中,我们聚焦于血管内皮细胞的神经节苷脂,并分析了它们在肿瘤血管生成中的功能。在人类乳腺癌中,GM3合酶在血管内皮细胞以及免疫细胞中高表达。GM3S基因敲除小鼠的血管生成增加。在牛主动脉内皮细胞(BAEC)中,GM3S的RNA干扰通过激活ERK显示出细胞侵袭增加和氧化应激耐受性增强。在乳腺癌模型中,GM3基因敲除小鼠的肿瘤生长和血管生成增加。这些结果表明,内皮神经节苷脂GM3通过抑制内皮细胞的细胞侵袭和氧化应激耐受性来调节肿瘤血管生成。