通过光化学内化增强抗robo1免疫毒素对头颈部鳞状细胞癌的细胞毒性

N. Komatsu, Kenichi Mitsui, Osamu Kusano-Arai, H. Iwanari, K. Hoshi, T. Takato, Takahiro Abe, T. Hamakubo
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引用次数: 5

摘要

背景:头颈部鳞状细胞癌(HNSCC)是全球第六大常见癌症。由于饮食失调、语言问题和美容问题,手术、化疗和放疗等标准治疗引起的长期并发症降低了生活质量(QOL)。近年来,抗体治疗因其提高生活质量的能力而日益受到重视。Robo1是一种轴突引导受体,作为一种单克隆抗体靶点在多种癌症中受到广泛关注。方法和结果:我们检测了Robo1的表达和皂苷偶联抗Robo1免疫毒素(IT)对几种HNSCC细胞系的细胞毒作用。使用抗体B5209B流式细胞术估计Robo1细胞表面表达水平在Robo1过表达的CHO (Robo1/ CHO)细胞中约为220,000拷贝,在HNSCCs中,HSQ-89细胞中为22,000拷贝,Sa3细胞中为3,000拷贝,inSAS细胞中为少量拷贝。即使在HSQ-89细胞中,传统的IT治疗也表现出不足的细胞毒性作用。添加光敏剂和LED光照(650 nm)后,HSQ89的细胞毒作用明显增强。随着暴露时间的延长,即使在Sa3细胞中也观察到明显的细胞毒性。结论:光化学内化(PCI)是一种很有前途的增强IT对肿瘤细胞毒性的方法。本研究显示的药物传递系统应适用于癌细胞上其他低水平表达的靶点,从而扩大罕见癌症的治疗窗口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancement of Anti-Robo1 Immunotoxin Cytotoxicity to Head and Neck Squamous Cell Carcinoma via Photochemical Internalization
Background: Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. The long-term complications arising from standard therapy with surgery, chemotherapy and radiotherapy lower the quality of life (QOL) due to eating disorders, speech problems and cosmetic issues. Recently the importance of antibody therapy has increasingly come to be recognized for its capacity to enhance QOL. Robo1, an axon guidance receptor, has been received considerable attention as a monoclonal antibody target in various cancers. Methods and findings: We checked the expression of Robo1 and the cytotoxic effect of saporin-conjugated anti- Robo1 immunotoxin (IT) against several HNSCC cell lines. The Robo1 cell surface expression level estimated by flow cytometry using the antibody B5209B was approximately 220,000 copies in Robo1 over-expressed CHO (Robo1/ CHO) cells, and in HNSCCs, 22,000 copies in HSQ-89 cells, 3,000 copies in Sa3 cells, and few copies inSAS cells. Conventional IT treatment exhibited an inadequate cytotoxic effect even in HSQ-89 cells. When we added a photosensitizer and LED light illumination (650 nm), the cytotoxic effect was remarkably improved in HSQ89. With longer exposure, significant cytotoxicity was observed, even in Sa3 cells. Conclusion: These results suggest that the photochemical internalization (PCI) is a promising method for augmenting the cytotoxicity of IT against tumors. The drug delivery system shown in this study should be applicable to other targets with low level expression on cancer cells, thus widening the therapeutic window in rare cancers.
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