Study on the Material Basis and Mechanisms of Achyrocline satureioides in the Treatment of Nonsmall Cell Lung Cancer Based on Network Pharmacology and Spatial Metabolomics

化学 代谢组学 药理学 癌症 肺癌 传统医学 肿瘤科 内科学 色谱法 医学
作者
Duo Shen,Jianxin Min,Jie Chen,Dongmei Yan,Jing Han,Huihui Liu,Yu Xi,Zongxiu Nie,Bin Li
出处
期刊:Analytical Chemistry [American Chemical Society]
标识
DOI:10.1021/acs.analchem.4c06682
摘要

Achyrocline satureioides have good therapeutic effects on nonsmall cell lung cancer (NSCLC). Nevertheless, it is still challenging to elucidate the active ingredients and mechanism of action due to their complex chemical composition. To address this, we innovatively combined network pharmacology with spatial metabolomics to comprehensively investigate the active components and the action mechanism in the present study. First, metabolomics of cells treated with the methanol extract of A. satureioides (ASM) utilizing high-resolution ultrahigh-performance liquid chromatography tandem mass spectrometry (HR-UHPLC-MS/MS) revealed 32 changed metabolites and 7 enriched metabolic pathways, confirming the anti-NSCLC effect of ASM and its impact on endogenous metabolites at the cellular level. Then, 69 chemical components in the ASM were identified using HR-UHPLC-MS/MS, followed by the screening of 6 core components and 10 core targets of anti-NSCLC with the help of network pharmacology and molecular docking. Lastly, quercetin, the most abundant compound among the six core active ingredients, was chosen for evaluating its anti-NSCLC effect and the potential mechanism using matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI). 51 altered endogenous metabolites were screened, and pathway enrichment analysis results were consistent with cell metabolomics, corroborating our network pharmacology predictions. In addition, we also observed the accumulation of three metabolites of quercetin in the tumor tissues. Network pharmacology combined with MSI elucidated the metabolic mechanisms by which A. satureioides treats NSCLC, offering new insights into herbal cancer therapies.
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
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
科研通AI5应助宝宝时代采纳,获得10
刚刚
研友_Lmb15n完成签到,获得积分10
1秒前
2秒前
猩心完成签到,获得积分10
2秒前
yoyo发布了新的文献求助10
3秒前
3秒前
小蘑菇应助纠纠采纳,获得10
4秒前
机灵安白完成签到 ,获得积分10
7秒前
是小越啊发布了新的文献求助10
8秒前
若邻完成签到,获得积分10
8秒前
8秒前
8秒前
edtaa发布了新的文献求助10
8秒前
文献看不懂应助入戏太深采纳,获得10
9秒前
LingYun完成签到,获得积分10
10秒前
mawanyu发布了新的文献求助30
13秒前
13秒前
Owen应助lwl采纳,获得10
14秒前
AA发布了新的文献求助10
14秒前
Abiu发布了新的文献求助10
20秒前
科研通AI5应助yaning2022采纳,获得10
21秒前
科研通AI5应助Zenglongying采纳,获得10
22秒前
laochen发布了新的文献求助10
26秒前
27秒前
34秒前
34秒前
小马甲应助meimei采纳,获得10
38秒前
无花果应助zhdjj采纳,获得10
38秒前
Zenglongying发布了新的文献求助10
39秒前
qiulong发布了新的文献求助10
41秒前
edtaa完成签到,获得积分10
42秒前
bkagyin应助复杂的访波采纳,获得10
43秒前
43秒前
44秒前
LL完成签到 ,获得积分10
45秒前
45秒前
lwl发布了新的文献求助10
47秒前
47秒前
琛哥物理完成签到,获得积分10
48秒前
1111发布了新的文献求助10
48秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Mindfulness and Character Strengths: A Practitioner's Guide to MBSP 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3776633
求助须知:如何正确求助?哪些是违规求助? 3322152
关于积分的说明 10208826
捐赠科研通 3037339
什么是DOI,文献DOI怎么找? 1666647
邀请新用户注册赠送积分活动 797603
科研通“疑难数据库(出版商)”最低求助积分说明 757921