Mansouri Vahid, Arjmand Babak, Hamzeloo-Moghadam Maryam, Rezaei Tavirani Mostafa, Razzaghi Zahra, Ahmadzadeh Alireza, Rostami Nejad Mohammad, Mohamoud Robati Reza
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.
J Lasers Med Sci. 2023 Aug 10;14:e25. doi: 10.34172/jlms.2023.25. eCollection 2023.
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.
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。