Epilepsy Research Center, Münster University, 48149 Münster, Germany; Department of Clinical Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran 1996835911, Iran.
Department of Neurosurgery, Münster University, 48149 Münster, Germany.
Life Sci. 2024 Aug 15;351:122808. doi: 10.1016/j.lfs.2024.122808. Epub 2024 Jun 7.
As a precursor of protoporphyrin IX (PpIX), an endogenous pro-apoptotic and fluorescent molecule, 5-Aminolevulinic acid (5-ALA) has gained substantial attention for its potential in fluorescence-guided surgery as well as photodynamic therapy (PDT). Moreover, 5-ALA-PDT has been suggested as a promising chemo-radio sensitization therapy for various cancers. However, insufficient 5-ALA-induced PpIX fluorescence and the induction of multiple resistance mechanisms may hinder the 5-ALA-PDT clinical outcome. Reduced efficacy and resistance to 5-ALA-PDT can result from genomic alterations, tumor heterogeneity, hypoxia, activation of pathways related to cell surveillance, production of nitric oxide, and most importantly, deregulated 5-ALA transporter proteins and heme biosynthesis enzymes. Understanding the resistance regulatory mechanisms of 5-ALA-PDT may allow the development of effective personalized cancer therapy. Here, we described the mechanisms underlying resistance to 5-ALA-PTD across various tumor types and explored potential strategies to overcome this resistance. Furthermore, we discussed future approaches that may enhance the efficacy of treatments using 5-ALA-PDT.
作为原卟啉 IX(PpIX)的前体,内源性促凋亡和荧光分子,5-氨基酮戊酸(5-ALA)因其在荧光引导手术和光动力疗法(PDT)中的潜力而备受关注。此外,5-ALA-PDT 已被提议作为各种癌症的有前途的化疗和放射增敏治疗方法。然而,5-ALA 诱导的 PpIX 荧光不足和多种耐药机制的诱导可能会阻碍 5-ALA-PDT 的临床效果。5-ALA-PDT 的疗效降低和耐药性可能源于基因组改变、肿瘤异质性、缺氧、与细胞监视相关的途径的激活、一氧化氮的产生,最重要的是,5-ALA 转运蛋白和血红素生物合成酶的失调。了解 5-ALA-PDT 的耐药调节机制可能有助于开发有效的个性化癌症治疗方法。在这里,我们描述了各种肿瘤类型中对 5-ALA-PTD 耐药的机制,并探讨了克服这种耐药性的潜在策略。此外,我们还讨论了未来可能增强使用 5-ALA-PDT 治疗效果的方法。