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褐藻苷苔多酚7-Polyphenol-Ecklonia抑制肿瘤转移和血管新生的研究 被引量:3
Study on the inhibitory effect of 7-Polyphenol-Ecklonia of the brown algae Ecklonia cava on tumor metastasis and angiogenesis
文献类型:期刊文献
中文题名:褐藻苷苔多酚7-Polyphenol-Ecklonia抑制肿瘤转移和血管新生的研究
英文题名:Study on the inhibitory effect of 7-Polyphenol-Ecklonia of the brown algae Ecklonia cava on tumor metastasis and angiogenesis
作者:杨胜涛[1];刘怡[2];萧振邦[2];黄晓洋[2];周春霞[1,3];千忠吉[2,3]
机构:[1]广东海洋大学食品科技学院,广东省水产品加工与安全重点实验室,广东省海洋食品工程技术研究中心,广东湛江524088;[2]广东海洋大学化学与环境学院,广东湛江524088;[3]南方海洋科学与工程广东省实验室,广东湛江524025
年份:2021
卷号:40
期号:2
起止页码:35
中文期刊名:中国海洋药物
外文期刊名:Chinese Journal of Marine Drugs
收录:CSTPCD、、CSCD、CSCD_E2021_2022
基金:广东省基础与应用基础研究基金项目(2020A1515011075);南方海洋科学与工程重点实验室(湛江)资助项目(ZJW-2019-07);湛江市海洋经济创新发展示范市建设项目(湛海创2017C8B1);广东海洋大学“大学生创新创业训练计划”项目(CXXL2020286)资助。
语种:中文
中文关键词:褐藻多酚;肿瘤转移;血管新生;金属基质蛋白酶;低氧诱导因子-1α
外文关键词:brown algae polyphenols;tumor metastasis;angiogenesis;MMPs;HIF-1α
中文摘要:目的探究海洋褐藻苷苔(Ecklonia cava)多酚7-polyphenol-ecklonia(7PE)对肿瘤侵袭转移和血管生成的影响。方法采用细胞毒性实验检测7PE分别对人成纤维肉瘤细胞(HT-1080)和人脐静脉内皮细胞(HUVEC)的毒性作用;划痕实验检测7PE对HT-1080细胞的迁移能力影响;明胶酶谱法和ELISA检测HT-1080细胞的金属基质蛋白酶-2/9(MMP-2/9)、低氧诱导因子-1α(HIF-1α)和血管内皮生长因子(VEGF)蛋白的表达水平;成管实验检测7PE对HUVEC成管的作用;分子对接模拟7PE与MMP-2/9和HIF-1α蛋白的相互作用。结果 7PE明显抑制HT-1080的迁移和MMP-2、MMP-9、VEGF和HIF-1α蛋白的表达;且能明显抑制HUVEC成管能力;此外与MMP-2/9和HIF-1α能形成稳定的相互作用。结论 7PE可抑制肿瘤细胞转移和血管新生,可作为研发抗肿瘤药物的活性物质。
外文摘要:Objective To explore the effect of marine brown algae Ecklonia cava polyphenol 7-polyphenol-ecklonia(7 PE) on tumor invasion, metastasis and angiogenesis. Methods Cytotoxicity experiments were used to detect the toxic effects of 7 PE on human fibrosarcoma cells(HT-1080) and human umbilical vein endothelial cells(HUVEC). The scratch test was used to examine the effect of 7 PE on the migration ability of HT-1080 cells. Gelatin zymography and ELISA were used to detect metal matrix proteinase-2/9(MMP-2/9), hypoxia inducible factor-1α(HIF-1α) and vascular endothelial growth factor(VEGF) protein expression level in HT-1080 cells. Tube forming experiment was used to detect the effect of 7 PE on HUVEC tube forming. Molecular docking was used to simulate the interaction of 7 PE with MMP-2/9 and HIF-1α protein, respectively. Results 7 PE obviously inhibited the migration of HT-1080 and the expression of MMP-2/9, VEGF, HIF-1α protein. And 7 PE obviously inhibited the HUVEC tube forming ability. Moreover, it could form stable interaction with MMP-2/9 and HIF-1α. Conclusion 7 PE could inhibit tumor cell metastasis and angiogenesis, and could be used as an active substance in the development of anti-tumor drugs.
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