PI3K/AKT/mTOR通路
癌症研究
蛋白激酶B
吉非替尼
MAPK/ERK通路
酪氨酸激酶
表皮生长因子受体
药理学
癌细胞
酪氨酸激酶抑制剂
肺癌
化学
激酶
信号转导
生物
癌症
医学
受体
生物化学
内科学
遗传学
作者
Jiaojiao Yu,Lijing Zhang,Jun Peng,Richard J. Ward,Peiqi Hao,Jiwei Wang,Na Zhang,Yang Yang,Xiao‐Xi Guo,Cheng Xiang,Su An,Tian‐Rui Xu
标识
DOI:10.1016/j.bcp.2021.114864
摘要
= 2.811 μM). Notably, Dic was shown to synergistically improve the chemo-sensitivity of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI)-resistant lung cancer cells to gefitinib and osimertinib. These results suggest that Dic is a c-Met inhibitor that can serve as a potential therapeutic agent in the treatment of lung cancer, especially against EGFR TKI-resistant and c-Met-dependent lung cancer.
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