转移
癌症研究
血管生成
车站3
斑马鱼
细胞生长
细胞凋亡
STAT蛋白
信号转导
焦点粘着
癌症
生物
化学
肺癌
细胞生物学
医学
病理
生物化学
遗传学
基因
作者
Yeling Li,Huimei Wang,Wenhui Liu,Jiantong Hou,Jing Xu,Yuanqiang Guo,Ping Hu
标识
DOI:10.3389/fphar.2022.920422
摘要
To discover phytochemicals as lead compounds for cancer treatment, cratoxylumxanthone C, a natural xanthone, was obtained from Cratoxylum cochinchinense (Lour.) Bl., for which there have been no reports on the biological effects against cancer . Our study revealed that cratoxylumxanthone C had significant anti-tumor activity by inducing apoptosis, augmenting cellular reactive oxygen species (ROS), and arresting cell circle. The mechanistic examination showed the inhibition of A549 cell proliferation and metastasis by cratoxylumxanthone C was coupled with the signal transducer and activator of transcription 3 (STAT3) and focal adhesion kinase (FAK) signaling pathways. Furthermore, the zebrafish models confirmed its significant in vivo anti-tumor activity, in which cratoxylumxanthone C inhibited tumor proliferation and metastasis and suppressed the angiogenesis. Comprehensively, these cellular and zebrafish experiments implied that cratoxylumxanthone C may have the potential to become an anti-tumor agent for lung cancer, especially non-small cell lung cancer (NSCLC).
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