细胞凋亡
A549电池
PI3K/AKT/mTOR通路
细胞培养
程序性细胞死亡
细胞生长
细胞生物学
氧化应激
化学
MAPK/ERK通路
蛋白激酶B
细胞
活性氧
MCF-7型
癌症研究
癌细胞
生物
癌症
磷酸化
生物化学
遗传学
人体乳房
作者
Gyeong Han Jeong,Dong‐Ho Bak,Hanui Lee,Ja Young Cho,Seong Hee Kang,Byung Yeoup Chung,Sanghwa Park,Hyoung‐Woo Bai
摘要
Abstract The huge diversity of secondary bioactive metabolites, such as antibiotic and anticancer compounds produced by Micromonospora sp., makes it an attractive target for study. Here, we explored the anti-proliferative activities of Micromonospora sp. M2 extract (MBE) in relation to its pro-oxidative activities in A549 and MCF7 cell lines. Anti-proliferative effects were assessed by treating cells with MBE. We found that treatment with MBE decreased cell proliferation and increased intracellular reactive oxygen species, and that these observations were facilitated by the suppression of the PI3K-AKT pathway, alterations to the Bcl/Bad ratio, and increased caspase activity. These observations also demonstrated that MBE induced apoptotic cell death in cell lines. In addition, the phosphorylation of P38 and c-Jun N-terminal kinase (JNK) were upregulated following MBE treatment in both cell lines. Collectively, these results indicate that MBE acts as an anticancer agent via oxidative stress and JNK/mitogen-activated protein kinase pathway activation, enhancing apoptotic cell death in cell lines.
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