Sakurai H, Mitsuhashi N, Kitamoto Y, Nonaka T, Harashima K, Higuchi K, Muramatsu H, Ebara T, Ishikawa H, Niibe H
Department of Radiology and Radiation Oncology, Gunma University School of Medicine, Japan.
Anticancer Res. 1998 Jul-Aug;18(4A):2525-8.
The aim of this study was to investigate the cell killing induced by low dose-rate irradiation (LDRI) simultaneously combined with long duration mild hyperthermia in LK87 human lung cancer cells. Cell cycle alteration due to this combined treatment was also observed.
Human lung adenocarcinoma cells, LK87, were treated with concurrent LDRI (50 cGy/hr) and mild hyperthermia (38 to 42 degrees C). Cell survival was estimated by clonogenic assay. Flow cytometry was performed with FACScan. The treatments were simultaneously performed for up to 48 hr (24 Gy).
Survival curves of mild hyperthermia alone revealed development of chronic thermotolerance up to 48 hr, whereas LDRI plus hyperthermia caused an exponential decrease in survival. The LDRI cytotoxicities were enhanced by mild hyperthermia over a non-lethal temperature range. The Do values calculated from dose response curves at 37, 38, 39, 40, 41 41.5 and 42 degrees C were 6.55, 5.25, 4.24, 3.99, 3.46, 1.83 and 0.70 Gy, respectively. Cell cycle analysis demonstrated a remarkable G2 and a mild G1 block for LDRI alone, but only a G1 block was observed for LDRI combined with 41 degrees C hyperthermia.
The LDRI cytotoxicity was enhanced by long duration mild temperature hyperthermia. The suppression of chronic thermotolerance was considered to be a mechanism involved in this sensitization.
本研究旨在探讨低剂量率照射(LDRI)与长时间轻度热疗同时联合作用于LK87人肺癌细胞所诱导的细胞杀伤作用。同时观察这种联合治疗引起的细胞周期改变。
人肺腺癌细胞LK87接受同步低剂量率照射(50 cGy/小时)和轻度热疗(38至42摄氏度)。通过克隆形成试验评估细胞存活率。使用FACScan进行流式细胞术分析。治疗同时进行长达48小时(24 Gy)。
单独轻度热疗的存活曲线显示,直至48小时出现慢性耐热性,而低剂量率照射加轻度热疗导致存活率呈指数下降。在非致死温度范围内,轻度热疗增强了低剂量率照射的细胞毒性。在37、38、39、40、41、41.5和42摄氏度下根据剂量反应曲线计算的Do值分别为6.55、5.25、4.24、3.99、3.46、1.83和0.70 Gy。细胞周期分析表明,单独低剂量率照射有显著的G2期阻滞和轻度的G1期阻滞,但低剂量率照射与41摄氏度热疗联合时仅观察到G1期阻滞。
长时间轻度温度热疗增强了低剂量率照射的细胞毒性。慢性耐热性的抑制被认为是这种增敏作用涉及的一种机制。