高级检索
当前位置: 首页 > 详情页

Alantolactone inhibits esophageal adenocarcinoma cells through nuclear factor erythroid 2-related factor 2-mediated ROS increment

文献详情

资源类型:
Pubmed体系:
机构: [1]Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong, China. [2]School of Basic Medical Sciences &amp [3]Forensic Medicine, North Sichuan Medical College, Nanchong, China. [3]Medical imaging Key Laboratory of Sichuan Province, North Sichuan Medical College, Nanchong, China. [4]Department of Anesthesiology, School of Clinical Medicine, North Sichuan Medical College, Nanchong, China. [5]Institute of Tissue Engineering and Stem Cells, Cancer Biotherapy Key Laboratory of Nanchong Nanchong Central Hospital, The Second Clinical Medical College, North Sichuan Medical College, Nanchong, China.
出处:
ISSN:

关键词: adenocarcinoma Alantolactone Nrf2 oesophageal ROS

摘要:
Esophageal adenocarcinoma (EAC) is a highly lethal cancer associated with a rapidly rising incidence and a poor prognosis. Alantolactone, a sesquiterpene lactone isolated from inula helenium, has anti-inflammatory, antimicrobial, neuroprotective activities, and anticancer properties.In the present study, the anticancer effects of alantolactone on the human EAC cells were investigated in vitro and in vivo.After treated with alantolactone, the cell viability of KYAE-1, KYAE-2, OE19, OE33 cells reduced significantly compared with that of the control cells. Alantolactone induced apoptosis of the EAC cell lines by inhibiting the protein expression levels of nuclear factor erythroid2-related factor 2 (Nrf2). Furthermore, the apoptosis-inducing effect of alantolactone was enhanced by Nrf2 knockdown, while reduced by over-expression of Nrf2. Anti-oxidant α-tocopherol and glutathione can protect EAC cell lines against alantolactone A xenograft nude mice model showed that alantolactone can inhibit EAC growth in vivo.Alantolactone inhibits esophageal adenocarcinoma cells through Nrf2-mediated Reactive oxygen species (ROS) increment. Alantolactone maybe a potential therapeutical candidate for treating EAC.This article is protected by copyright. All rights reserved.

基金:
语种:
PubmedID:
中科院(CAS)分区:
出版当年[2022]版:
大类 | 3 区 医学
小类 | 3 区 毒理学 3 区 药学
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 药学 4 区 毒理学
第一作者:
第一作者机构: [1]Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong, China.
共同第一作者:
通讯作者:
通讯机构: [1]Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong, China. [*1]Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong 637100, China.
推荐引用方式(GB/T 7714):
APA:
MLA:

资源点击量:43377 今日访问量:0 总访问量:3120 更新日期:2024-09-01 建议使用谷歌、火狐浏览器 常见问题

版权所有©2020 四川省肿瘤医院 技术支持:重庆聚合科技有限公司 地址:成都市人民南路四段55号