• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[寻常型银屑病不同中医证型特征基因的筛选:基于生物信息学和机器学习的研究]

[Screening for Characteristic Genes of Different Traditional Chinese Medicine Syndromes of Psoriasis Vulgaris: A Study Based on Bioinformatics and Machine Learning].

作者信息

Liu Xuewei, Jia Huangchao, Wang Liyun, Wang Ziwen, Xu Mengyue, Li Yunfei, Wang Ronghui

机构信息

( 450046) Henan University of Chinese Medicine, Zhengzhou 450046, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2024 Mar 20;55(2):337-345. doi: 10.12182/20240360402.

DOI:10.12182/20240360402
PMID:38645867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11026890/
Abstract

OBJECTIVE

To screen for the key characteristic genes of the psoriasis vulgaris (PV) patients with different Traditional Chinese Medicine (TCM) syndromes, including blood-heat syndrome (BHS), blood stasis syndrome (BSS), and blood-dryness syndrome (BDS), through bioinformatics and machine learning and to provide a scientific basis for the clinical diagnosis and treatment of PV of different TCM syndrome types.

METHODS

The GSE192867 dataset was downloaded from Gene Expression Omnibus (GEO). The limma package was used to screen for the differentially expressed genes (DEGs) of PV, BHS, BSS, and BDS in PV patients and healthy populations. In addition, KEGG (Kyoto Encyclopedia of Genes and Genes) pathway enrichment analysis was performed. The DEGs associated with PV, BHS, BSS, and BDS were identified in the screening and were intersected separately to obtain differentially characterized genes. Out of two algorithms, the support vector machine (SVM) and random forest (RF), the one that produced the optimal performance was used to analyze the characteristic genes and the top 5 genes were identified as the key characteristic genes. The receiver operating characteristic (ROC) curves of the key characteristic genes were plotted by using the pROC package, the area under curve () was calculated, and the diagnostic performance was evaluated, accordingly.

RESULTS

The numbers of DEGs associated with PV, BHS, BSS, and BDS were 7699, 7291, 7654, and 6578, respectively. KEGG enrichment analysis was focused on Janus kinase (JAK)/signal transducer and activator of transcription (STAT), cyclic adenosine monophosphate (cAMP), mitogen-activated protein kinase (MAPK), apoptosis, and other pathways. A total of 13 key characteristic genes were identified in the screening by machine learning. Among the 13 key characteristic genes, malectin ), TUB like protein 3 (3), SET domain containing 9 (9), nuclear envelope integral membrane protein 2 (2), and BTG anti-proliferation factor 3 (3) were the key characteristic genes of BHS; phosphatase 15 (15), C1q and tumor necrosis factor related protein 7 (17), solute carrier family 12 member 5 (125), tripartite motif containing 63 (63), and ubiquitin associated protein 1 like (1) were the key characteristic genes of BSS; recombinant mouse protein (1), GTPase-activating protein ASAP3 Protein (3), and human myomesin 2 (2) were the key characteristic genes of BDS. Moreover, all of them showed high diagnostic efficacy.

CONCLUSION

There are significant differences in the characteristic genes of different PV syndromes and they may be potential biomarkers for diagnosing TCM syndromes of PV.

摘要

目的

通过生物信息学和机器学习筛选寻常型银屑病(PV)不同中医证型,包括血热证(BHS)、血瘀证(BSS)和血燥证(BDS)的关键特征基因,为PV不同中医证型的临床诊断和治疗提供科学依据。

方法

从基因表达综合数据库(GEO)下载GSE192867数据集。使用limma软件包筛选PV患者及健康人群中PV、BHS、BSS和BDS的差异表达基因(DEGs)。此外,进行京都基因与基因组百科全书(KEGG)通路富集分析。在筛选出的与PV、BHS、BSS和BDS相关的DEGs中分别进行交集运算,以获得差异特征基因。在支持向量机(SVM)和随机森林(RF)两种算法中,选择性能最优的算法分析特征基因,并将排名前5的基因确定为关键特征基因。使用pROC软件包绘制关键特征基因的受试者工作特征(ROC)曲线,计算曲线下面积(AUC),并据此评估诊断性能。

结果

与PV、BHS、BSS和BDS相关的DEGs数量分别为7699、7291、7654和6578。KEGG富集分析聚焦于Janus激酶(JAK)/信号转导子和转录激活子(STAT)、环磷酸腺苷(cAMP)、丝裂原活化蛋白激酶(MAPK)、凋亡等通路。通过机器学习筛选共鉴定出13个关键特征基因。在这13个关键特征基因中,malectin、微管样蛋白3(TUB like protein 3)、含SET结构域蛋白9(SET domain containing 9)、核膜整合膜蛋白2(nuclear envelope integral membrane protein 2)和BTG抗增殖因子3(BTG anti-proliferation factor 3)是BHS的关键特征基因;蛋白磷酸酶15(phosphatase 15)、C1q和肿瘤坏死因子相关蛋白7(C1q and tumor necrosis factor related protein 7)、溶质载体家族12成员5(solute carrier family 12 member 5)、含三联基序蛋白63(tripartite motif containing 63)和泛素相关蛋白1样蛋白(ubiquitin associated protein 1 like)是BSS的关键特征基因;重组小鼠蛋白(recombinant mouse protein)、GTP酶激活蛋白ASAP3(GTPase-activating protein ASAP3 Protein)和人肌间蛋白2(human myomesin 2)是BDS的关键特征基因。而且,它们均显示出较高的诊断效能。

结论

PV不同证型的特征基因存在显著差异,可能是PV中医证型诊断的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/3363c4a9b7b0/scdxxbyxb-55-2-337-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/4a1579cc7263/scdxxbyxb-55-2-337-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/a271bd1547e6/scdxxbyxb-55-2-337-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/852374967ca2/scdxxbyxb-55-2-337-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/c07c757a02fa/scdxxbyxb-55-2-337-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/76ca8819ea6c/scdxxbyxb-55-2-337-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/3363c4a9b7b0/scdxxbyxb-55-2-337-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/4a1579cc7263/scdxxbyxb-55-2-337-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/a271bd1547e6/scdxxbyxb-55-2-337-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/852374967ca2/scdxxbyxb-55-2-337-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/c07c757a02fa/scdxxbyxb-55-2-337-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/76ca8819ea6c/scdxxbyxb-55-2-337-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2921/11026890/3363c4a9b7b0/scdxxbyxb-55-2-337-6.jpg

相似文献

1
[Screening for Characteristic Genes of Different Traditional Chinese Medicine Syndromes of Psoriasis Vulgaris: A Study Based on Bioinformatics and Machine Learning].[寻常型银屑病不同中医证型特征基因的筛选:基于生物信息学和机器学习的研究]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2024 Mar 20;55(2):337-345. doi: 10.12182/20240360402.
2
Correlation analysis of Treg/Th17 cells and related cytokines in patients with psoriasis vulgaris.寻常型银屑病患者 Treg/Th17 细胞及其相关细胞因子的相关性分析。
J Tradit Chin Med. 2019 Oct;39(5):700-706.
3
Integrated bioinformatics combined with machine learning to analyze shared biomarkers and pathways in psoriasis and cervical squamous cell carcinoma.综合生物信息学结合机器学习分析银屑病和宫颈鳞状细胞癌中的共享生物标志物和通路。
Front Immunol. 2024 May 28;15:1351908. doi: 10.3389/fimmu.2024.1351908. eCollection 2024.
4
Key genes and immune infiltration patterns and the clinical implications in psoriasis patients.银屑病患者的关键基因和免疫浸润模式及其临床意义。
Skin Res Technol. 2024 Aug;30(8):e13889. doi: 10.1111/srt.13889.
5
Screening COPD-Related Biomarkers and Traditional Chinese Medicine Prediction Based on Bioinformatics and Machine Learning.基于生物信息学和机器学习的 COPD 相关生物标志物筛选及中医药预测。
Int J Chron Obstruct Pulmon Dis. 2024 Sep 24;19:2073-2095. doi: 10.2147/COPD.S476808. eCollection 2024.
6
Expression of T-helper 17 cells and signal transducers in patients with psoriasis vulgaris of blood-heat syndrome and blood-stasis syndrome.寻常型银屑病血热证和血瘀证患者中辅助性T细胞17及信号转导分子的表达
Chin J Integr Med. 2015 Jan;21(1):10-6. doi: 10.1007/s11655-014-1769-7. Epub 2014 Sep 23.
7
The immune status of patients with psoriasis vulgaris of blood-stasis syndrome and blood-dryness syndrome: a qualitative evidence synthesis.血瘀证和血燥证寻常型银屑病患者的免疫状态:定性证据综合分析。
Ann Palliat Med. 2020 Jul;9(4):1382-1395. doi: 10.21037/apm-19-432. Epub 2020 Jul 14.
8
A comprehensive analysis of m6A/m7G/m5C/m1A-related gene expression and immune infiltration in liver ischemia-reperfusion injury by integrating bioinformatics and machine learning algorithms.通过整合生物信息学和机器学习算法对肝脏缺血再灌注损伤中m6A/m7G/m5C/m1A相关基因表达及免疫浸润进行综合分析
Eur J Med Res. 2024 Jun 13;29(1):326. doi: 10.1186/s40001-024-01928-y.
9
Immune-associated biomarkers identification for diagnosing carotid plaque progression with uremia through systematical bioinformatics and machine learning analysis.通过系统生物信息学和机器学习分析鉴定用于诊断尿毒症颈动脉斑块进展的免疫相关生物标志物。
Eur J Med Res. 2023 Feb 23;28(1):92. doi: 10.1186/s40001-023-01043-4.
10
Discovery of biomarkers in the psoriasis through machine learning and dynamic immune infiltration in three types of skin lesions.通过机器学习和三种皮肤损伤中的动态免疫浸润发现银屑病的生物标志物。
Front Immunol. 2024 May 13;15:1388690. doi: 10.3389/fimmu.2024.1388690. eCollection 2024.

本文引用的文献

1
Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background.全外显子组测序和生物信息学分析揭示了伴有和不伴有良性甲状腺肿背景的甲状腺乳头状癌患者基因突变谱的差异。
Front Endocrinol (Lausanne). 2023 Jan 4;13:1039494. doi: 10.3389/fendo.2022.1039494. eCollection 2022.
2
Psoriasis complicated with metabolic disorder is associated with traditional Chinese medicine syndrome types: a hospital-based retrospective case-control study.银屑病合并代谢紊乱与中医证候类型的相关性:一项基于医院的回顾性病例对照研究。
Curr Med Res Opin. 2023 Jan;39(1):19-25. doi: 10.1080/03007995.2022.2129803. Epub 2022 Oct 11.
3
CTRP7 Is a Biomarker Related to Insulin Resistance and Oxidative Stress: Cross-Sectional and Intervention Studies In and In .
CTRP7 是与胰岛素抵抗和氧化应激相关的生物标志物:横断面和干预研究在 和 中。
Oxid Med Cell Longev. 2022 Mar 23;2022:6877609. doi: 10.1155/2022/6877609. eCollection 2022.
4
TULP3 silencing suppresses cell proliferation, migration and invasion in gastric cancer via the PTEN/Akt/Snail pathway.TULP3基因沉默通过PTEN/Akt/Snail信号通路抑制胃癌细胞的增殖、迁移和侵袭。
Cancer Treat Res Commun. 2022;31:100551. doi: 10.1016/j.ctarc.2022.100551. Epub 2022 Mar 23.
5
Selenium-Rich Yeast Peptide Fraction Ameliorates Imiquimod-Induced Psoriasis-like Dermatitis in Mice by Inhibiting Inflammation via MAPK and NF-κB Signaling Pathways.富硒酵母肽通过抑制 MAPK 和 NF-κB 信号通路改善咪喹莫特诱导的小鼠银屑病样皮炎。
Int J Mol Sci. 2022 Feb 14;23(4):2112. doi: 10.3390/ijms23042112.
6
The JAK/STAT signaling pathway: from bench to clinic.JAK/STAT 信号通路:从基础到临床。
Signal Transduct Target Ther. 2021 Nov 26;6(1):402. doi: 10.1038/s41392-021-00791-1.
7
Metabolic Syndrome and Skin Diseases.代谢综合征与皮肤病
Front Endocrinol (Lausanne). 2019 Nov 20;10:788. doi: 10.3389/fendo.2019.00788. eCollection 2019.
8
Targeting the Janus Kinase Family in Autoimmune Skin Diseases.靶向自身免疫性皮肤病中的 Janus 激酶家族。
Front Immunol. 2019 Oct 9;10:2342. doi: 10.3389/fimmu.2019.02342. eCollection 2019.
9
Cutaneous p38 mitogen-activated protein kinase activation triggers psoriatic dermatitis.皮肤 p38 丝裂原活化蛋白激酶的激活引发银屑病。
J Allergy Clin Immunol. 2019 Oct;144(4):1036-1049. doi: 10.1016/j.jaci.2019.06.019. Epub 2019 Aug 1.
10
Psoriasis Pathogenesis and Treatment.银屑病发病机制与治疗。
Int J Mol Sci. 2019 Mar 23;20(6):1475. doi: 10.3390/ijms20061475.