Identification of Key Genes and Related Drugs of Adrenocortical Carcinoma by Integrated Bioinformatics Analysis

肾上腺皮质癌 鉴定(生物学) 基因 生物信息学 内科学 钥匙(锁) 内分泌学 计算生物学 医学 生物 肿瘤科 癌症研究 遗传学 生态学 植物
作者
Jian-bin Wei,Xiaochun Zeng,Kui-rong Ji,Lingyi Zhang,Xiaomin Chen
出处
期刊:Hormone and Metabolic Research [Georg Thieme Verlag KG]
卷期号:56 (08): 593-603 被引量:1
标识
DOI:10.1055/a-2209-0771
摘要

Adrenocortical carcinoma (ACC) is a malignant carcinoma with an extremely poor prognosis, and its pathogenesis remains to be understood to date, necessitating further investigation. This study aims to discover biomarkers and potential therapeutic agents for ACC through bioinformatics, enhancing clinical diagnosis and treatment strategies. Differentially expressed genes (DEGs) between ACC and normal adrenal cortex were screened out from the GSE19750 and GSE90713 datasets available in the GEO database. An online Venn diagram tool was utilized to identify the common DEGs between the two datasets. The identified DEGs were subjected to functional assessment, pathway enrichment, and identification of hub genes by performing the protein-protein interaction (PPI), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. The differences in the expressions of hub genes between ACC and normal adrenal cortex were validated at the GEPIA2 website, and the association of these genes with the overall patient survival was also assessed. Finally, on the QuartataWeb website, drugs related to the identified hub genes were determined. A total of 114 DEGs, 10 hub genes, and 69 known drugs that could interact with these genes were identified. The GO and KEGG analyses revealed a close association of the identified DEGs with cellular signal transduction. The 10 hub genes identified were overexpressed in ACC, in addition to being significantly associated with adverse prognosis in ACC. Three genes and the associated known drugs were identified as potential targets for ACC treatment.

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
可爱的函函应助棋子采纳,获得10
刚刚
1秒前
碧蓝寄风发布了新的文献求助10
2秒前
sci_zt发布了新的文献求助10
2秒前
3秒前
王欣蔚发布了新的文献求助10
3秒前
3秒前
4秒前
4秒前
5秒前
muBai嘎嘎牛完成签到,获得积分10
5秒前
曹婷婷完成签到,获得积分10
5秒前
默幻弦完成签到,获得积分10
6秒前
WEAWEA应助月白采纳,获得10
8秒前
8秒前
happyou发布了新的文献求助10
9秒前
9秒前
danny完成签到 ,获得积分10
10秒前
10秒前
秦王爱碳水完成签到,获得积分10
10秒前
10秒前
东农dhl完成签到 ,获得积分10
10秒前
FashionBoy应助细心的语蓉采纳,获得10
11秒前
11秒前
13秒前
QQ发布了新的文献求助10
13秒前
13秒前
gugu完成签到,获得积分10
13秒前
淡然的夜柳应助大迷糊采纳,获得10
13秒前
14秒前
rxdeng发布了新的文献求助10
14秒前
大壮完成签到 ,获得积分10
14秒前
hhhh发布了新的文献求助10
14秒前
15秒前
肥仔龙完成签到,获得积分10
15秒前
rookie完成签到,获得积分20
17秒前
Lucky应助鹅女士采纳,获得30
18秒前
希望天下0贩的0应助无钱采纳,获得10
18秒前
Orange应助pretty采纳,获得10
19秒前
19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
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Digital Twins of Advanced Materials Processing 2000
Propeller Design 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
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 纳米技术 化学工程 生物化学 物理 计算机科学 内科学 复合材料 催化作用 物理化学 光电子学 电极 冶金 细胞生物学 基因
热门帖子
关注 科研通微信公众号,转发送积分 6015605
求助须知:如何正确求助?哪些是违规求助? 7594203
关于积分的说明 16149448
捐赠科研通 5163387
什么是DOI,文献DOI怎么找? 2764357
邀请新用户注册赠送积分活动 1745025
关于科研通互助平台的介绍 1634761