Pewklang Thitima, Chansaenpak Kantapat, Bakar Siti Nursyahirah, Lai Rung-Yi, Kue Chin Siang, Kamkaew Anyanee
School of Chemistry, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
National Nanotechnology Center, National Science and Technology Development Agency, Thailand Science Park, Pathum Thani, Thailand.
Front Chem. 2022 Nov 2;10:1015883. doi: 10.3389/fchem.2022.1015883. eCollection 2022.
Hypoxia caused by photodynamic therapy (PDT) is a major hurdle to cancer treatment since it can promote recurrence and progression by activating angiogenic factors, lowering therapeutic efficacy dramatically. In this work, AZB-I-CAIX was developed as a carbonic anhydrase IX (CAIX)-targeting NIR photosensitizer that can overcome the challenge by utilizing a combination of CAIX knockdown and PDT. AZB-I-CAIX showed a specific affinity to CAIX-expressed cancer cells and enhanced photocytotoxicity compared to AZB-I-control (the molecule without acetazolamide). Moreover, selective detection and effective cell cytotoxicity of AZB-I-CAIX by PDT in hypoxic CAIX-expressed murine cancer cells were achieved. Essentially, AZB-I-CAIX could minimize tumor size in the tumor-bearing mice compared to that in the control groups. The results suggested that AZB-I-CAIX can improve therapeutic efficiency by preventing PDT-induced hypoxia through CAIX inhibition.
光动力疗法(PDT)引起的缺氧是癌症治疗的一个主要障碍,因为它可通过激活血管生成因子促进复发和进展,从而显著降低治疗效果。在这项研究中,AZB-I-CAIX被开发为一种靶向碳酸酐酶IX(CAIX)的近红外光敏剂,它可以通过结合CAIX基因敲低和PDT来克服这一挑战。与AZB-I对照(不含乙酰唑胺的分子)相比,AZB-I-CAIX对表达CAIX的癌细胞表现出特异性亲和力,并增强了光细胞毒性。此外,通过PDT在缺氧的表达CAIX的小鼠癌细胞中实现了AZB-I-CAIX的选择性检测和有效的细胞毒性。从本质上讲,与对照组相比,AZB-I-CAIX可以使荷瘤小鼠的肿瘤大小最小化。结果表明,AZB-I-CAIX可通过抑制CAIX来预防PDT诱导的缺氧,从而提高治疗效率。