Arjmand Babak, Bahadorimonfared Ayad, Jahani Sherafat Somayeh, Moravvej Hamideh, Rezaei Mitra, Daneshimehr Fatemeh, Asri Nastaran, Farahani Masoumeh
Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Iranian Cancer Control Center (MACSA), Tehran, Iran.
J Lasers Med Sci. 2024 Dec 24;15:e67. doi: 10.34172/jlms.2024.67. eCollection 2024.
Photodynamic therapy (PDT) is a photochemical treatment that involves the use of light and photosensitizer. This method is applied as a therapeutic approach against several types of cancer. The main aim of this study is to compare the efficacy of PDT with that of cisplatin (a well-known chemotherapy agent) through protein-protein interaction (PPI) network analysis. Gene expression profiles of human melanoma A375 cells from the Gene Expression Omnibus (GEO) were selected for analysis via directed PPI network analysis. The significant differentially expressed genes (DEGs) were identified and assessed based on co-expression interactions. The critical DEGs were introduced by considering out-degree and in-degree values. Two directed PPI networks for upregulated and downregulated DEGs were constructed. TP53 was identified as a critical upregulated gene in response to cisplatin in comparison with PDT. EGFR, PPARG, MMP9, PTGS2, FOXO1, and RUNX2 were highlighted as the crucial downregulated genes due to the effect of cisplatin on the gene expression of the treated cells. Cisplatin directly targets key cellular functions such as cell growth, differentiation, migration, and invasion. It seems that the combination of cisplatin and PDT is a suitable method for treating cancers because cisplatin targets the key genes responsible for cancer development, while PDT intensifies the effect of cisplatin and reduces its side effects.
光动力疗法(PDT)是一种涉及使用光和光敏剂的光化学治疗方法。该方法被用作针对几种癌症类型的治疗手段。本研究的主要目的是通过蛋白质-蛋白质相互作用(PPI)网络分析来比较PDT与顺铂(一种知名的化疗药物)的疗效。从基因表达综合数据库(GEO)中选择人类黑色素瘤A375细胞的基因表达谱,通过定向PPI网络分析进行分析。基于共表达相互作用鉴定并评估显著差异表达基因(DEG)。通过考虑出度和入度值引入关键DEG。构建了上调和下调DEG的两个定向PPI网络。与PDT相比,TP53被鉴定为对顺铂有反应的关键上调基因。由于顺铂对处理后细胞基因表达的影响,表皮生长因子受体(EGFR)、过氧化物酶体增殖物激活受体γ(PPARG)、基质金属蛋白酶9(MMP9)、环氧化酶-2(PTGS2)、叉头框蛋白O1(FOXO1)和 runt相关转录因子2(RUNX2)被突出显示为关键下调基因。顺铂直接靶向细胞生长、分化、迁移和侵袭等关键细胞功能。顺铂和PDT的联合似乎是治疗癌症的合适方法,因为顺铂靶向负责癌症发展的关键基因,而PDT增强顺铂的作用并降低其副作用。