Masunaga Shin-Ichiro, Tano Keizo, Sanada Yu, Suzuki Minoru, Takahashi Akihisa, Ohnishi Ken, Ono Koji
Particle Radiation Biology, Institute for Integrated Radiation and Nuclear Science, Kyoto University, 2-1010, Asashiro-nishi, Kumatori-cho, Sennan-gun, Osaka 590-0494, Japan.
Particle Radiation Oncology, Institute for Integrated Radiation and Nuclear Science, Kyoto University, 2-1010, Asashiro-nishi, Kumatori-cho, Sennan-gun, Osaka 590-0494, Japan.
World J Oncol. 2019 Jun;10(3):132-141. doi: 10.14740/wjon1203. Epub 2019 Jun 29.
The aim of the study was to examine the dependency of status and the usefulness of mild hyperthermia (MHT) as an inhibitor of recovery from radiation-induced damage, referring to the response of quiescent (Q) tumor cell population.
Human head and neck squamous cell carcinoma cells transfected with mutant (SAS/) or with neo vector (SAS/) were injected subcutaneously into left hind legs of nude mice. Tumor-bearing mice received 5-bromo-2'-deoxyuridine (BrdU) continuously to label all intratumor proliferating (P) cells. They received high dose-rate γ-ray irradiation (HDR) immediately followed by localized MHT (40 °C for 2 h), or caffeine or wortmannin administration, or low dose-rate γ-ray irradiation simultaneously with localized MHT or caffeine or wortmannin administration. Nine hours after the start of irradiation, the tumor cells were isolated and incubated with a cytokinesis blocker, and the micronucleus (MN) frequency in cells without BrdU labeling (= Q cells) was determined using immunofluorescence staining for BrdU.
SAS/ tumor cells, especially intratumor Q cell populations, showed a marked reduction in sensitivity due to the recovery from radiation-induced damage, compared with the total or Q tumor cells within SAS/ tumors that showed little recovery capacity. The recovery from radiation-induced damage was thought to be a dependent event. In both total and Q tumor cells within SAS/ tumors, especially the latter, MHT efficiently suppressed the reduction in sensitivity caused by leaving an interval between HDR irradiation and the assay and decreasing the irradiation dose-rate, as well as the combination with wortmannin administration.
From the viewpoint of solid tumor control as a whole, including intratumor Q-cell control, non-toxic MHT is useful for suppressing the recovery from radiation-induced damage, as well as wortmannin treatment combined with γ-ray irradiation.
本研究旨在参照静止(Q)肿瘤细胞群的反应,探讨状态依赖性以及轻度热疗(MHT)作为辐射诱导损伤恢复抑制剂的有效性。
将转染了突变体(SAS/)或新载体(SAS/)的人头颈鳞状细胞癌皮下注射到裸鼠的左后肢。荷瘤小鼠持续接受5-溴-2'-脱氧尿苷(BrdU)以标记所有肿瘤内增殖(P)细胞。它们接受高剂量率γ射线照射(HDR),随后立即进行局部MHT(40℃,2小时),或给予咖啡因或渥曼青霉素,或在局部MHT、咖啡因或渥曼青霉素给药的同时进行低剂量率γ射线照射。照射开始9小时后,分离肿瘤细胞并与胞质分裂阻滞剂一起孵育,使用针对BrdU的免疫荧光染色测定未标记BrdU的细胞(=Q细胞)中的微核(MN)频率。
与几乎没有恢复能力的SAS/肿瘤内的全部或Q肿瘤细胞相比,SAS/肿瘤细胞,尤其是肿瘤内Q细胞群,由于从辐射诱导损伤中恢复而显示出敏感性显著降低。辐射诱导损伤的恢复被认为是一个依赖性事件。在SAS/肿瘤内的全部和Q肿瘤细胞中,尤其是后者,MHT有效地抑制了由于在HDR照射和检测之间留出间隔以及降低照射剂量率而导致的敏感性降低,以及与渥曼青霉素给药联合导致的敏感性降低。
从包括肿瘤内Q细胞控制在内的实体瘤整体控制的角度来看,无毒的MHT对于抑制辐射诱导损伤的恢复是有用的,与γ射线照射联合的渥曼青霉素治疗也是如此。