Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein 2028, South Africa.
Int J Mol Sci. 2023 Jan 31;24(3):2656. doi: 10.3390/ijms24032656.
Photodynamic therapy (PDT) holds great promise in cancer eradication due to its target selectivity, non-invasiveness, and low systemic toxicity. However, due to the hypoxic nature of many native tumors, PDT is frequently limited in its therapeutic effect. Additionally, oxygen consumption during PDT may exacerbate the tumor's hypoxic condition, which stimulates tumor proliferation, metastasis, and invasion, resulting in poor treatment outcomes. Therefore, various strategies have been developed to combat hypoxia in PDT, such as oxygen carriers, reactive oxygen supplements, and the modulation of tumor microenvironments. However, most PDT-related studies are still conducted on two-dimensional (2D) cell cultures, which fail to accurately reflect tissue complexity. Thus, three-dimensional (3D) cell cultures are ideal models for drug screening, disease simulation and targeted cancer therapy, since they accurately replicate the tumor tissue architecture and microenvironment. This review summarizes recent advances in the development of strategies to overcome tumor hypoxia for enhanced PDT efficiency, with a particular focus on nanoparticle-based photosensitizer (PS) delivery systems, as well as the advantages of 3D cell cultures.
光动力疗法(PDT)由于其靶向选择性、非侵入性和低全身毒性,在癌症治疗中具有很大的应用前景。然而,由于许多原发性肿瘤的缺氧性质,PDT 的治疗效果经常受到限制。此外,PDT 期间的氧气消耗可能会加剧肿瘤的缺氧状态,刺激肿瘤增殖、转移和侵袭,导致治疗效果不佳。因此,已经开发了各种策略来对抗 PDT 中的缺氧,例如氧载体、活性氧补充剂和肿瘤微环境的调节。然而,大多数与 PDT 相关的研究仍在二维(2D)细胞培养物上进行,这无法准确反映组织的复杂性。因此,三维(3D)细胞培养物是药物筛选、疾病模拟和靶向癌症治疗的理想模型,因为它们准确地复制了肿瘤组织的结构和微环境。本综述总结了克服肿瘤缺氧以提高 PDT 效率的策略的最新进展,特别关注基于纳米颗粒的光敏剂(PS)递送系统,以及 3D 细胞培养物的优势。