Yanase Shigeaki, Nomura Jouji, Matsumura Yoshihiko, Nagata Takayuki, Fujii Tasuku, Tagawa Toshiro
Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Mie University, Tsu, Mie 514-8507, Japan.
Int J Oncol. 2006 Aug;29(2):365-73.
In this study, the effectiveness and mechanism of combination therapy of 5-aminolevulinic acid-based photodynamic therapy (ALA-PDT) with simultaneous hyperthermia (HT) on human-derived osteosarcoma in vivo were examined. A tumor model was prepared by subcutaneously implanting human osteosarcoma into nude mice and local injection of ALA was selected as the administration route. This study demonstrated that both ALA-PDT and the combination of ALA-PDT with HT exhibited significant inhibitory effects on tumor growth. In the group with high total energy, the growth inhibition rates of tumor were 52.3% in ALA-PDT, and 27.3% in ALA-PDT with simultaneous HT (PDT+HT), and the synergetic index was 1.76, demonstrating that the inhibitory effect on tumor growth in ALA-PDT was significantly increased by simultaneous use of HT. In the histological findings, after ALA-PDT, necrosis was observed in the area from the surface to a depth of 2 mm, and only a slight effect was confirmed in deeper layers. On the other hand, after PDT+HT, necrosis was observed in layers even deeper than 2 mm below the surface. Furthermore, based on the immunohistochemical findings of the expression of carbonic anhydrase IX, while weak expression of CAIX was observed after ALA-PDT in an area relatively close to the surface, a positive area extended to the deeper layers after PDT+HT compared with ALA-PDT. In conclusion, PDT+HT demonstrated a significant inhibitory effect on tumor growth of human-derived osteosarcoma, and a synergistic interaction of simultaneous HT. This suggests the possibility that ALA-PDT is useful, not only for the treatment of superficial tumors but also for deep-seated mesenchymal tumors, such as osteosarcoma. Furthermore, the mechanism of the synergistic interaction suggested that ALA-PDT was effective in the deep area of tumors due to the increase of blood flow by mild hyperthermia.
在本研究中,检测了基于5-氨基酮戊酸的光动力疗法(ALA-PDT)联合同步热疗(HT)对人源骨肉瘤体内治疗的有效性及机制。通过将人骨肉瘤皮下植入裸鼠制备肿瘤模型,并选择局部注射ALA作为给药途径。本研究表明,ALA-PDT以及ALA-PDT联合HT均对肿瘤生长具有显著抑制作用。在高总能量组中,ALA-PDT组肿瘤生长抑制率为52.3%,ALA-PDT联合同步HT(PDT+HT)组为27.3%,协同指数为1.76,表明同步使用HT可显著增强ALA-PDT对肿瘤生长的抑制作用。组织学检查结果显示,ALA-PDT后,从表面至2mm深度区域出现坏死,更深层仅见轻微影响。另一方面,PDT+HT后,表面以下2mm更深层均见坏死。此外,基于碳酸酐酶IX表达的免疫组化结果,ALA-PDT后在相对靠近表面区域观察到CAIX弱表达,与ALA-PDT相比,PDT+HT后阳性区域扩展至更深层。总之,PDT+HT对人源骨肉瘤肿瘤生长具有显著抑制作用及同步HT的协同作用。这提示ALA-PDT不仅对浅表肿瘤治疗有用,对骨肉瘤等深部间叶组织肿瘤也可能有用。此外,协同作用机制表明,轻度热疗增加血流量使得ALA-PDT在肿瘤深部区域有效。