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摘要:
Glioblastoma is carcinogenesis of glial cells in central nervous system and has the highest incidence among primary brain tumors.Brain metastasis,such as breast cancer and lung cancer,also leads to high mortality.The available medicines are limited due to blood-brain barrier.Abnormal acti-vation of phosphatidylinositol 3-kinases(PI3K)signaling pathway is prevalent in glioblastoma and met-astatic tumors.Here,we characterized a 2-amino-4-methylquinazoline derivative XH30 as a potent PI3K inhibitor with excellent anti-tumor activity against human glioblastoma.XH30 significantly repressed the proliferation of various brain cancer cells and decreased the phosphorylation of key proteins of PI3K signaling pathway,induced cell cycle arrest in G1 phase as well.Additionally,XH30 inhibited the migra-tion of glioma cells and blocked the activation of PI3K pathway by interleukin-17A(IL-17A),which increased the migration of U87MG.Oral administration of XH30 significantly suppressed the tumor growth in both subcutaneous and orthotopic tumor models.XH30 also repressed tumor growth in brain metastasis models of lung cancers.Moreover,XH30 reduced IL-17A and its receptor LL-17RA in vivo.These results indicate that XH30 might be a potential therapeutic drug candidate for glioblastoma migra-tion and brain metastasis.
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篇名 A novel PI3K inhibitor XH30 suppresses orthotopic glioblastoma and brain metastasis in mice models
来源期刊 药学学报(英文版) 学科
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年,卷(期) 2022,(2) 所属期刊栏目 Original articles
研究方向 页码范围 774-786
页数 13页 分类号
字数 语种 英文
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药学学报(英文版)
双月刊
2211-3835
10-1171/R
北京市先农坛街1号
eng
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688
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