Hederagenin promotes lung cancer cell death by activating CHAC1-dependent ferroptosis pathway

蛇床子素 肺癌 程序性细胞死亡 癌症 癌症研究 化学 医学 生物 细胞凋亡 病理 内科学 生物化学 替代医学 齐墩果酸
作者
Jiayan Lu,Qing-Yi Guo,Hui Zhao,Hua Liu
出处
期刊:Biochemical and Biophysical Research Communications [Elsevier]
卷期号:718: 150085-150085
标识
DOI:10.1016/j.bbrc.2024.150085
摘要

Lung cancer poses a significant threat globally, especially in China. This puts higher demands on the treatment methods and drugs for lung cancer. Natural plants provide valuable resources for the development of anti-cancer drugs. Hederagenin (Hed) is a triterpenoid compound extracted from ivy leaves and has anti-tumor activity against multifarious cancers, including lung cancer. However, the regulatory mechanism of Hed in lung cancer remains unclear. In this study, we used Hed to treat lung cancer cells, and observed the effect of Hed on cell proliferation (including CCK-8 and colony formation experiments), apoptosis (including flow cytometry and apoptosis gene detection (BAX and Bcl-2)). The results showed that Hed induced lung cancer cell death (inhibiting proliferation and promoting apoptosis). Next, we performed bioinformatics analysis of the expression profile GSE186218 and found that Hed treatment significantly increased the expression of CHAC1 gene. CHAC1 is a ferroptosis-inducing gene. RT-qPCR detection of lung cancer clinical tissues and related cell lines also showed that CHAC1 was lowly expressed in lung cancer. Therefore, we knocked down and overexpressed CHAC1 in lung cancer cells, respectively. Subsequently, cell phenotype experiments showed that down-regulating CHAC1 expression inhibited lung cancer cell death (promoting proliferation and inhibiting apoptosis); on the contrary, up-regulating CHAC1 expression promoted lung cancer cell death. To further verify that Hed exerts anti-tumor effects in lung cancer by promoting CHAC1 expression, we performed functional rescue experiments. The results showed that down-regulating CHAC1 expression reversed the promoting effect of Hed on lung cancer cell death. Mechanistically, in vitro and in vivo experiments jointly demonstrated that Hed exerts anti-cancer effects by promoting CHAC1-induced ferroptosis. In summary, our study further enriches the regulatory mechanism of Hed in lung cancer.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
布鲁布鲁完成签到 ,获得积分10
1秒前
大模型应助小白努力呀采纳,获得10
2秒前
小昼完成签到 ,获得积分10
2秒前
酷波er应助独特乘云采纳,获得10
2秒前
2秒前
Orochimaru发布了新的文献求助20
2秒前
3秒前
小西完成签到,获得积分10
3秒前
怡然涵双发布了新的文献求助10
3秒前
有来有去完成签到,获得积分10
3秒前
3秒前
llbeyond应助柯基小胖采纳,获得10
4秒前
阳光海云完成签到,获得积分10
4秒前
5秒前
街道办事部完成签到,获得积分10
5秒前
坚定尔安完成签到,获得积分10
6秒前
Puddingo完成签到,获得积分10
6秒前
8秒前
怜熙发布了新的文献求助10
8秒前
Lucas应助有来有去采纳,获得10
8秒前
胡萝卜z完成签到 ,获得积分10
9秒前
愉快的曼文完成签到,获得积分10
9秒前
lzz发布了新的文献求助10
10秒前
白水完成签到,获得积分10
10秒前
11秒前
机智的琪完成签到,获得积分10
11秒前
Eason215xB完成签到,获得积分10
11秒前
橘子完成签到,获得积分10
11秒前
11秒前
程鹏程发布了新的文献求助10
12秒前
三月完成签到,获得积分20
12秒前
完美世界应助453采纳,获得10
12秒前
13秒前
fixit发布了新的文献求助10
13秒前
13秒前
13秒前
华东小可爱完成签到,获得积分10
13秒前
英姑应助七安采纳,获得10
14秒前
JamesPei应助anlikek采纳,获得10
15秒前
Lucas应助caicai采纳,获得10
15秒前
高分求助中
Impact of Mitophagy-Related Genes on the Diagnosis and Development of Esophageal Squamous Cell Carcinoma via Single-Cell RNA-seq Analysis and Machine Learning Algorithms 2000
Evolution 1100
How to Create Beauty: De Lairesse on the Theory and Practice of Making Art 1000
Gerard de Lairesse : an artist between stage and studio 670
CLSI EP47 Evaluation of Reagent Carryover Effects on Test Results, 1st Edition 550
Sport, Music, Identities 500
T/CAB 0344-2024 重组人源化胶原蛋白内毒素去除方法 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 2985405
求助须知:如何正确求助?哪些是违规求助? 2646313
关于积分的说明 7146750
捐赠科研通 2279857
什么是DOI,文献DOI怎么找? 1209481
版权声明 592326
科研通“疑难数据库(出版商)”最低求助积分说明 590682