子宫内膜癌
溶酶体
癌症研究
PI3K/AKT/mTOR通路
活力测定
氯硝柳胺
程序性细胞死亡
自噬
癌细胞
癌症
细胞凋亡
蛋白激酶B
组织蛋白酶D
组织蛋白酶B
化学
生物
药理学
医学
内科学
酶
生物化学
生态学
作者
Rajani Rai,Debasish Kumar Dey,Doris M. Benbrook,Vishal Chandra
标识
DOI:10.1016/j.biopha.2023.114422
摘要
Endometrial cancer is the most common female cancer showing continuous rise in its incidence and mortality rate. Despite the extensive research efforts in cancer therapeutics, still there is a lack of effective treatment options and the outcome is poor for patients with advanced and recurrent endometrial cancers. In this study, we aimed to evaluate the efficacy of niclosamide (NIC) against endometrial cancer. NIC is an FDA-approved anti-helminthic drug, which has been recently extensively studied as a potent anti-cancerous agent in several cancers. The anti-cancerous activity of NIC was analyzed in-vitro (ANC3A, Hec1B, and Ishikawa endometrial cancer cell lines) by cell viability-, soft agar-, invasion- and migration- assay. The action mechanism of NIC was demonstrated by western blot analysis and immune-fluorescence imaging and validated by specific inhibitors. The in-vivo efficacy of NIC was studied in the Ishikawa xenograft animal model. NIC effectively suppressed the viability (IC
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