Sumi Shigeki, Umemura Naoki, Adachi Makoto, Ohta Takahisa, Naganawa Kosuke, Kawaki Harumi, Takayama Eiji, Kondoh Nobuo, Sumitomo Shinichiro
Department of Oral and Maxillofacial Surgery Asahi University School of Dentistry Japan.
Department of Oral Biochemistry Asahi University School of Dentistry Japan.
Clin Exp Dent Res. 2018 Aug 15;4(5):174-181. doi: 10.1002/cre2.126. eCollection 2018 Oct.
The aim of this research was to investigate the value of autofluorescence imaging of oral cancer across different stages of tumor growth, to assist in detecting tumors. A xenograft mouse model was created with human oral squamous cell carcinoma cell line HSC-3 being subcutaneously inoculated into nude mice. Tumor imaging was performed with an autofluorescence imaging method (Illumiscan®) using the luminance ratio, which was defined as the luminance of the tumor site over the luminance of normal skin tissue normalized to a value of 1.0. This luminance ratio was continuously observed postinoculation. Tumor and normal skin tissues were harvested, and differences in the concentrations of flavin adenine dinucleotide and nicotinamide adenine dinucleotide were examined. The luminance ratio of the tumor sites was 0.85 ± 0.05, and there was no significant change in the ratio over time, even if the tumor proliferated and expanded. Furthermore, flavin adenine dinucleotide and nicotinamide adenine dinucleotide were significantly lower in tumor tissue than in normal skin tissue. A luminance ratio under 0.90 indicates a high possibility of tumor, irrespective of the tumor growth stage. However, this cutoff value was determined using a xenograft mouse model and therefore requires further validation before being used in clinical diagnosis.
本研究的目的是探讨口腔癌在肿瘤生长不同阶段的自体荧光成像价值,以辅助检测肿瘤。通过将人口腔鳞状细胞癌细胞系HSC-3皮下接种到裸鼠体内,建立了异种移植小鼠模型。使用亮度比,通过自体荧光成像方法(Illumiscan®)对肿瘤进行成像,亮度比定义为肿瘤部位的亮度与正常皮肤组织亮度之比,并将其归一化为1.0。接种后持续观察该亮度比。采集肿瘤和正常皮肤组织,检测黄素腺嘌呤二核苷酸和烟酰胺腺嘌呤二核苷酸的浓度差异。肿瘤部位的亮度比为0.85±0.05,即使肿瘤增殖和扩大,该比值随时间也无显著变化。此外,肿瘤组织中的黄素腺嘌呤二核苷酸和烟酰胺腺嘌呤二核苷酸明显低于正常皮肤组织。无论肿瘤生长阶段如何,亮度比低于0.90表明肿瘤可能性高。然而,该临界值是使用异种移植小鼠模型确定的,因此在用于临床诊断之前需要进一步验证。