A549电池
内吞作用
细胞生物学
MAPK/ERK通路
生物
蛋白激酶A
信号转导
细胞生长
癌症研究
癌细胞
细胞凋亡
细胞
激酶
癌症
生物化学
遗传学
作者
Minhui Zhang,Jack Ho Wong,F. Liu,Tzi Bun Ng,Zhao-Kun Liu
标识
DOI:10.1016/j.ijbiomac.2022.12.061
摘要
Lung cancer has the highest mortality among cancer-related deaths worldwide. Among lung cancers, non-small cell lung cancer (NSCLC) is the most common histological type. In the previous research, we isolated a protein (D1) from Boletus bicolor that inhibits the proliferation of NSCLC cell lines. In this study, we elucidated the internalization mechanism and antitumor mechanism of protein D1 in A549 cells. Protein D1 has a strong inhibitory effect on A549 cells. It binds to secretory carrier membrane protein 3 on the A549 cell membrane and enters A549 cells by clathrin-mediated endocytosis. In vitro, protein D1 activates mitogen-activated protein kinase (MAPK) signaling pathway. JNK and p38MAPK are the biological targets for protein D1. In vivo, protein D1 inhibits the tumor growth of NSCLC xenografts by inducing apoptosis and inhibiting cell proliferation. Protein D1 alters the expression of genes related to apoptosis, cell cycle, and MAPK signaling pathway in tumor cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI