已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Integrating Network Pharmacology and Experimental Verification to Explore the Pharmacological Mechanisms of Aloin Against Gastric Cancer

小桶 计算生物学 AKT1型 PI3K/AKT/mTOR通路 生物 交互网络 蛋白激酶B 基因本体论 基因 信号转导 生物化学 基因表达
作者
Jia Gao,Sifu Yang,Guanqun Xie,Jieli Pan,Feiye Zhu
出处
期刊:Drug Design Development and Therapy [Dove Medical Press]
卷期号:Volume 16: 1947-1961 被引量:31
标识
DOI:10.2147/dddt.s360790
摘要

This study was designed to evaluate the pharmacological mechanisms of Aloin against gastric cancer (GC) via network pharmacology analysis combined with experimental verification.Using network pharmacology methods, the potential targets of Aloin and targets related to GC were screened from public databases. The protein-protein interaction (PPI) network, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were performed to predict the core targets and pathways of Aloin against GC. The expressions of major targets predicted by network pharmacology in normal stomach tissues and GC tissues and their relationships with overall survival of GC were searched in GEPIA, HPA and DriverDBv3 database. The results of network pharmacology analysis were verified by in vitro experiments.A total of 129 potential targets were retrieved by searching the intersection of Aloin and GC targets. PPI network analysis indicated that 10 targets, including AKT1 and CASP3, were hub genes. GO enrichment analysis involved 93 biological processes, 19 cellular components, and 37 molecular functions. KEGG enrichment analysis indicated that the anti-cancer effect of Aloin was mediated through multiple pathways, such as PI3K-AKT, FoxO and Ras signaling pathway. Among them, the PI3K-AKT signaling pathway, which contained the largest number of enriched genes, may play a greater role in the treatment of GC. The validation of key targets in GEPIA, HPA and DriverDBv3 database showed that the verification results for most core genes were consistent with this study. Then, the results of in vitro experiment indicated that Aloin could inhibit proliferation of NCI-N87 cells and induce cell apoptosis. The results also showed that Aloin could decrease the mRNA and protein expressions of PI3K and AKT, suggesting that Aloin can treat GC by inducing cell apoptosis and regulating the PI3K-AKT signaling pathway.This study identified the potential targets of Aloin against GC using network pharmacology and in vitro verification, which provided a new understanding of the pharmacological mechanisms of Aloin in treatment of GC.
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
文不叮发布了新的文献求助10
刚刚
2秒前
冻结完成签到 ,获得积分10
4秒前
呆瓜不会飞关注了科研通微信公众号
4秒前
bkagyin的应助被山居月采纳,获得10
5秒前
秘书完成签到 ,获得积分10
6秒前
6秒前
科研通AI6.4的应助被一方采纳,获得10
7秒前
10秒前
积木师whale完成签到,获得积分10
11秒前
Owen的应助被青苹果采纳,获得10
11秒前
Jack完成签到 ,获得积分10
11秒前
CipherSage的应助被愉快的依霜采纳,获得20
12秒前
12秒前
12秒前
12秒前
13秒前
万能图书馆的应助被Oguri_Cap采纳,获得10
13秒前
14秒前
14秒前
14秒前
受伤的问蕊完成签到,获得积分10
14秒前
14秒前
yatuitui的应助被99采纳,获得10
16秒前
AdamJie发布了新的文献求助20
16秒前
huxiao发布了新的文献求助10
17秒前
wvs完成签到 ,获得积分10
17秒前
小马发布了新的文献求助10
18秒前
幸运幸福发布了新的文献求助10
18秒前
18秒前
难过妙柏发布了新的文献求助10
18秒前
sss发布了新的文献求助10
19秒前
Richard发布了新的文献求助10
19秒前
baihualin完成签到,获得积分10
19秒前
Enieeuu发布了新的文献求助10
19秒前
万能图书馆的应助被文不叮采纳,获得10
20秒前
Owen的应助被闪闪的草莓采纳,获得10
20秒前
21秒前
科目三的应助被huxiao采纳,获得10
23秒前
23秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Roman Family in Italy: Status, Sentiment, Space 2000
Aspects of Post-SPE Phonology 2000
Recombinant human Type III collagen with native-like assembly and real biomaterial performance 1000
CLSI VET01S Ed7 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals 1000
Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals 888
Rosenblum, Global Change Biology 800
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 物理 有机化学 化学工程 内科学 生物化学 复合材料 催化作用 心理学 细胞生物学 无机化学 电极 光电子学 人工智能
热门帖子
关注 科研通微信公众号,转发送积分 7871907
求助须知:如何正确求助?哪些是违规求助? 9388378
关于积分的说明 20768142
捐赠科研通 7473161
什么是DOI,文献DOI怎么找? 3351077
关于科研通互助平台的介绍 2491989
邀请新用户注册赠送积分活动 2377937