雷公藤甲素通过抑制聚乳胺链的合成抑制MCF-7和HepG2细胞的侵袭和迁移

Yaqing Yuan, Hao Qiu, Gao Jingdong, Z. Wang, Chunlian Liu, Zhenhua Liu, Zhi Jiang, Li Yongjian, Wu Shiliang
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引用次数: 1

摘要

雷公藤甲素是从传统中草药雷公藤中分离得到的具有生物活性的天然产物。临床研究显示雷公藤甲素可用于自身免疫性疾病,如类风湿关节炎、肾脏疾病和系统性红斑狼疮。近年来,一些研究发现雷公藤甲素具有抗肿瘤作用,越来越受到人们的关注。本实验旨在探讨雷公藤甲素与n型聚乳胺抗肿瘤作用的关系。随着雷公藤甲素浓度的增加,MCF-7和HepG2细胞的活力明显降低,多乳糖胺在这些细胞上的表达也下降。此外,参与催化n型聚乳糖胺合成的β 1,3 - n -乙酰氨基葡萄糖转移酶(β3GnT8)的表达也降低,下游信号传导基因和蛋白的表达也随之改变。最后,雷公藤甲素可以减弱癌细胞的侵袭和迁移。这些都表明雷公藤甲素通过下调聚乳胺链的表达来影响MCF-7和HepG2细胞的侵袭和迁移。这些研究表明雷公藤甲素是一种潜在的治疗乳腺癌和肝癌的新药物。
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Triptolide Inhibits MCF-7 and HepG2 Cells Invasion and Migration by Inhibiting the Synthesis of Polylactosamine Chains
Triptolide is a bioactive natural products isolated from Tripterygium wilfordii, a traditional Chinese herbal medicine. Clinical studies reveal that triptolide can be used in autoimmune disorders, such as rheumatoid arthritis, kidney disease and systemic lupus erythematosus. Recently, some studies revealed that triptolide has anti-tumor effects, which attracts more and more attention. This experiment aimed to explore the relationship between anti-tumor effects of triptolide and N-type polylactosamine. With increasing the concentration of triptolide, the viability of MCF-7 and HepG2 cells was reduced significantly and the polylactosamine expression on these cells declined as well. In addition, the expression of β1, 3-N-acetylglucosamine transferase (β3GnT8) participated in catalyzing the synthesis of N-type polylactosamine was also decreased and the expression of genes and proteins of downstream signaling was altered consequently. Finally, triptolide weakened the cancer cells invasion and migration. All of these indicate that triptolide can impair MCF-7 and HepG2 cells invasion and migration through downregulating the expression of polylactosamine chains. These studies establish that triptolide is a potential novel therapy in breast cancer and hepatic carcinoma.
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