赫拉
蛋白激酶B
细胞凋亡
MAPK/ERK通路
癌症研究
细胞生长
细胞周期
PI3K/AKT/mTOR通路
细胞生物学
信号转导
化学
生物
癌细胞
细胞
癌症
医学
内科学
生物化学
作者
Zhiqiang Hu,Hui Wang,Yan Fu,Kang Ma,Xiaoyan Ma,Jing Wang
标识
DOI:10.1080/01635581.2020.1801777
摘要
Cervical cancer (CC) is a common gynecological malignancy and represents a major global health challenge. Chemotherapeutic agents are commonly applied in treatment of CC, while along various adverse effects and chemotherapy resistance. As an iridoid glycoside compound, gentiopicroside (GPS) possesses the characteristic of the better availability and lower toxicity effect on cancer treatment. In the present study, we investigated that GPS exhibited the anticancer effect on HeLa cells through the inhibition of cell growth, induced apoptosis, cycle arrest, and suppressed migration. Furthermore, the possible mechanism or the targets of GPS was also clarified. The results revealed that GPS exerted an anti-proliferation effect in a dose- and time-dependent manner in HeLa cells, in contrast, with the less inhibiting proliferation effects on normal cell line (HUVEC). Moreover, GPS arrested cells at G2/M phase and induced apoptosis through mitochondrial apoptotic pathway. More significantly, GPS dramatically inhibited the migration of HeLa cells and regulated the matrix metalloproteinase expression through the MAPK and Akt signaling pathways, of which MAPK1 was an underlying target in GPS against HeLa cells.
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