MAPK/ERK通路
p38丝裂原活化蛋白激酶
蛋白激酶A
柴胡
肝癌
信号转导
分泌物
细胞生物学
癌症研究
癌细胞
免疫系统
激酶
细胞外
癌症
生物
药理学
化学
医学
免疫学
生物化学
内科学
中医药
病理
替代医学
作者
Xianmei Li,Liang‐Ying Liu,Gang Shi
标识
DOI:10.1177/09731296251346317
摘要
Background Bupleurum is an active ingredient extracted from the Chinese medicine bupleurum, which has been proven to have various biological effects, such as anti-tumor, anti-inflammatory, and immune regulation. However, its application is limited by factors such as low bioavailability and poor stability. In addition, extracellular vesicle secretion by liver cancer cells is involved in the formation and progression of liver cancer. The p38 mitogen-activated protein kinase (MAPK) and interleukin (IL)-6 pathways are two signaling pathways related to the development of liver cancer. Purpose By modifying SiNPs and bupleurum, we tried to inhibit these two signaling pathways to achieve a therapeutic effect on liver cancer. Materials and Methods HepG2 cells were cultured and used in group experiments to explore how bupleurum regulates the p38 MAPK/IL-6 pathway and exerts inhibition by using SB202190, p38 MAPK agonists, and inhibitors and agonists of IL-6 in liver cancer. Results SiNPs-SS has a stronger inhibitory effect on liver cancer than SS and inhibits the secretion of extracellular vesicles and progression of liver cancer by inhibiting the p38 MAPK/IL-6 pathway. Conclusion SiNPs-SS inhibits the secretion of extracellular vesicles and the progression of liver cancer by inhibiting the p38 MAPK/IL-6 pathway.
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