PI3K/AKT/mTOR通路
mTOR抑制剂的发现与发展
癌症
癌细胞
细胞生长
细胞凋亡
癌症研究
药理学
医学
生物
内科学
生物化学
作者
Yujiao Hou,Feifei Lv,Wenjing Zhai,Weina Wang,Yanhao Duan,Shanshan Liu,Yongle Qiu
出处
期刊:Science of Advanced Materials
[American Scientific Publishers]
日期:2022-09-01
卷期号:14 (9): 1466-1475
标识
DOI:10.1166/sam.2022.4369
摘要
Oral cancer is one of the 10 most common cancers in the world, which brings heavy burden for public health. Although several drugs were recommended to treat oral cancer, while it is needed to investigate the pathogenesis and develop novel treatment for this type of cancer. In the study, two oral cancer cell lines including HSC-6 and CAL-27 were used. It was found that rapamycin potently inhibited proliferation of HSC-6 and CAL-27 cells. Rapamycin significantly induced apoptosis and reduced cell viability of HSC-6 and CAL-27 cells. Rapamycin inhibited growth of oral cancer cells via mTOR. Moreover, it was found that mTOR was highly expresses in PBMC of oral cancer patients compared with PBMC of healthy controls. Rapamycin increased expression of miR-199a-3p and miR-199-3p was highly expression in oral cancer patients. Importantly, it was confirmed that rapamycin suppressed proliferation and promoted apoptosis of oral cancer cells via miR-199a-3p. The findings of the present study will provide useful insights for developing novel therapies of oral cancer.
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