企业档案
会员类型:标准版
已获得阿仪网信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
阿仪网标准版会员:8年
最后认证时间:无需年检
注册号:**** 【已认证】
法人代表:谭春** 【已认证】
参观次数:2676310
技术文章
人子宫内膜腺癌细胞HEC265(文献引用产品)
点击次数:797 发布时间:2026/4/21 15:43:47
文章标题:Osthole suppresses the proliferation and induces apoptosis via inhibiting the PI3K/AKT signaling pathway of endometrial cancer JEC cells
作者列表:Lei Liang, Bo Yang, Yuanyuan Wu, Li Sun
期刊:Experimental and Therapeutic Medicine
发表时间:2021-8-13
影响因子:2.447
DOI:10.3892/etm.2021.10605
主要研究成果:Abstract
Osthole, a natural product extracted mainly from fruits of Fructus Cnidii, possesses multiple pharmacological functions, including anti‑inflammatory, anti‑convulsant and anticancer effects. However, the effects of osthole in endometrial cancer (EC) is not fully understood. In the present study, EC cell lines, including JEC, KLE and Ishikawa cells and normal human cervical epithelial cells (HcerEpic) were applied to detect the anticancer effect of osthole. The present study demonstrated that osthole inhibited the proliferation of JEC, KLE and Ishikawa cells, but had no cytotoxic effect on HcerEpic. Furthermore, treatment of osthole induced JEC cell apoptosis, while osthole promoted the release of pro‑apoptotic proteins, Bax and activated the cleaved caspase‑3, caspase‑9 and PARP. Additionally, osthole significantly increased the expression of PETN and decreased the phosphorylated form of PI3K and AKT in a concentration‑dependent manner. Furthermore, osthole treatment suppressed the JEC tumor cell growth in a nude mouse xenograft model in vivo, and neither renal toxicity nor hepatotoxicity was induced by the indicated concentration. Taken together, the results of the present study suggested that osthole may be a novel and potential therapeutic agent of EC.

原创作者:上海雅吉生物科技有限公司






