Nakada Yusuke, Sugihara Takaaki, Tanaka Maria, Hamamoto Wataru, Kanda Tsutomu, Sakaguchi Takuki, Kurumi Hiroki, Onoyama Takumi, Ikebuchi Yuichiro, Takata Tomoaki, Isomoto Hajime, Yamaguchi Naoyuki
Division of Gastroenterology and Nephrology, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago 683-8504, Japan.
Department of Endoscopy, Nagasaki University Hospital, Nagasaki 852-85011, Japan.
Gastroenterology Res. 2024 Apr;17(2):72-81. doi: 10.14740/gr1694. Epub 2024 Apr 30.
Photodynamic therapy (PDT) has advanced through the utilization of photosensitizers and specific-wavelength light (≥ 600 nm). However, the widespread adoption of PDT is still impeded by high equipment costs and stringent laser safety requirements. Porphyrins, crucial in PDT, have another absorbance peak of blue light (λ = 380 - 500 nm). This peak corresponds to the wavelength of narrow-band imaging (NBI) (λ = 390 - 445 nm), an image-enhancement technology integrated into endoscopes by Olympus Medical Systems. The study aimed to investigate the potential of widely adopted NBI as a PDT light source for superficial cancers via endoscopes.
Esophageal and biliary cancers were selected for investigation. Human esophageal cancer cell lines (KYSE30, KYSE70, KYSE170) and cholangiocarcinoma cell lines (HuCCT-1, KKU-213) were subjected to verteporfin-mediated PDT under NBI light (λ = 390 - 445 nm). Assessments included spectrometry, crystal violet staining, and fluorescein imaging of singlet oxygen generation and apoptosis.
Verteporfin exhibited a peak (λ = 436 nm) consistent with the NBI spectrum, suggesting compatibility with NBI light. NBI light significantly inhibited the growth of esophageal and biliary cancer cells. The half-maximum effective concentration (EC) values (5 J/cm) for KYSE30, KYSE70, KYSE170, HuCCT-1, and KKU-213 were calculated as 2.78 ± 0.37µM, 1.76 ± 1.20 µM, 0.77 ± 0.16 µM, 0.65 ± 0.18 µM, and 0.32 ± 0.04 µM, respectively. Verteporfin accumulation in mitochondria, coupled with singlet oxygen generation and observed apoptotic changes, suggests effective PDT under NBI light.
NBI is a promising PDT light source for superficial cancers via endoscopes.
光动力疗法(PDT)通过使用光敏剂和特定波长的光(≥600nm)得到了发展。然而,PDT的广泛应用仍然受到高设备成本和严格激光安全要求的阻碍。卟啉在PDT中至关重要,它还有一个蓝光吸收峰(λ = 380 - 500nm)。这个峰对应窄带成像(NBI)的波长(λ = 390 - 445nm),NBI是一种由奥林巴斯医疗系统集成到内窥镜中的图像增强技术。本研究旨在探讨广泛应用的NBI作为通过内窥镜用于浅表癌的PDT光源的潜力。
选择食管癌和胆管癌进行研究。将人食管癌细胞系(KYSE30、KYSE70、KYSE170)和胆管癌细胞系(HuCCT - 1、KKU - 213)置于NBI光(λ = 390 - 445nm)下进行维替泊芬介导的PDT。评估包括光谱分析、结晶紫染色以及对单线态氧生成和细胞凋亡的荧光成像。
维替泊芬呈现出与NBI光谱一致的峰(λ = 436nm),表明与NBI光兼容。NBI光显著抑制了食管和胆管癌细胞的生长。KYSE30、KYSE70、KYSE170、HuCCT - 1和KKU - 213的半数最大有效浓度(EC)值(5J/cm)分别计算为2.78±0.37µM、1.76±1.20µM、0.77±0.16µM、0.65±0.18µM和0.32±0.04µM。维替泊芬在线粒体中的积累,以及单线态氧的生成和观察到的凋亡变化,表明在NBI光下PDT有效。
NBI是一种有前景的通过内窥镜用于浅表癌的PDT光源。