Suppr超能文献

介绍光动力疗法相关关键基因:网络分析

Introducing Critical Genes in Response to Photodynamic Therapy: A Network Analysis.

作者信息

Mansouri Vahid, Arjmand Babak, Hamzeloo-Moghadam Maryam, Rezaei Tavirani Mostafa, Razzaghi Zahra, Ahmadzadeh Alireza, Rostami Nejad Mohammad, Mohamoud Robati Reza

机构信息

Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

J Lasers Med Sci. 2023 Aug 10;14:e25. doi: 10.34172/jlms.2023.25. eCollection 2023.

Abstract

Photodynamic therapy (PDT) is applied as an efficient method for preventing the progress of cancers. Light and a photosensitive compound which is known as photosensitizer (PS) are the main parts of PDT. In the present study, molecular events after using PDT in the presence of a super lethal dose of a PS were assessed via protein-protein interaction (PPI) analysis. Data were extracted from Gene Expression Omnibus (GEO). The gene expression profiles of the treated human Sk-Cha1 cells via PDT were compared with the control cells. Expressed change analysis and PPI network analysis were administrated via Cytoscape software v 3.7.2 to find the critical differentially expressed genes (DEGs). Regulatory relationships between the central DEGs were evaluated and the highlighted genes were identified. The significant amounts of gene expression values were grouped and a few DEGs characterized by tremendously expressed values were identified. EGFR, CANX, HSPA5, MYC, JUN, ITGB1, APP, and CDH1 were highlighted as hub-bottleneck DEGs. EGFR, CDH1, and JUN appeared as a set of SEGs, which play a crucial role in response to PDT in the treated Sk-Cha1 cells. In conclusion, regulatory relationships between EGFR, CDH1, and JUN, which have an effect on the regulation of cellular survival, differentiation, and proliferation, were highlighted in the present investigation.

摘要

光动力疗法(PDT)是一种用于预防癌症进展的有效方法。光和一种被称为光敏剂(PS)的光敏化合物是PDT的主要组成部分。在本研究中,通过蛋白质-蛋白质相互作用(PPI)分析评估了在超致死剂量的PS存在下使用PDT后的分子事件。数据从基因表达综合数据库(GEO)中提取。将经PDT处理的人Sk-Cha1细胞的基因表达谱与对照细胞进行比较。通过Cytoscape软件v 3.7.2进行表达变化分析和PPI网络分析,以找到关键的差异表达基因(DEG)。评估了中心DEG之间的调控关系,并鉴定了突出的基因。对大量基因表达值进行分组,并鉴定了一些具有极高表达值特征的DEG。表皮生长因子受体(EGFR)、钙网蛋白(CANX)、热休克蛋白家族A成员5(HSPA5)、原癌基因MYC、原癌基因JUN、整合素β1(ITGB1)、淀粉样前体蛋白(APP)和钙黏蛋白1(CDH1)被突出显示为枢纽瓶颈DEG。EGFR、CDH1和JUN作为一组信号转导和转录激活因子(SEG)出现,它们在经处理的Sk-Cha1细胞对PDT的反应中起关键作用。总之,本研究突出了EGFR、CDH1和JUN之间的调控关系,这些关系对细胞存活、分化和增殖的调节有影响。

相似文献

6
Evaluation of Laser Intensity Effect on Photodynamic Therapy Efficacy.激光强度对光动力疗法疗效的影响评估
J Lasers Med Sci. 2024 Aug 4;15:e33. doi: 10.34172/jlms.2024.33. eCollection 2024.
8
Evaluation of cellular response to toxin-A: a network analysis.细胞对毒素A反应的评估:一项网络分析
Gastroenterol Hepatol Bed Bench. 2022;15(4):421-425. doi: 10.22037/ghfbb.v15i4.2634.

本文引用的文献

2
Photodynamic Therapy-Current Limitations and Novel Approaches.光动力疗法——当前的局限性与新方法
Front Chem. 2021 Jun 10;9:691697. doi: 10.3389/fchem.2021.691697. eCollection 2021.
3
Molecular and evolutionary processes generating variation in gene expression.基因表达变异的分子和进化过程。
Nat Rev Genet. 2021 Apr;22(4):203-215. doi: 10.1038/s41576-020-00304-w. Epub 2020 Dec 2.
6
Muscle Recovery Is Highlighted by IR Laser Therapy.红外激光疗法对肌肉恢复效果显著。
J Lasers Med Sci. 2019 Fall;10(Suppl 1):S49-S53. doi: 10.15171/jlms.2019.S9. Epub 2019 Dec 1.
8
The role of photodynamic therapy on multidrug resistant breast cancer.光动力疗法在多药耐药乳腺癌中的作用。
Cancer Cell Int. 2019 Apr 11;19:91. doi: 10.1186/s12935-019-0815-0. eCollection 2019.
9
Photodynamic therapy - mechanisms, photosensitizers and combinations.光动力疗法——机制、光敏剂及联合治疗。
Biomed Pharmacother. 2018 Oct;106:1098-1107. doi: 10.1016/j.biopha.2018.07.049. Epub 2018 Jul 17.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验