Masunaga Shin-Ichiro, Sanada Yu, Moriwaki Takahiro, Tano Keizo, Sakurai Yoshinori, Tanaka Hiroki, Suzuki Minoru, Kondo Natsuko, Narabayashi Masaru, Watanabe Tsubasa, Nakagawa Yosuke, Maruhashi Akira, Ono Koji
Department of Radiation Life and Medical Science, Research Reactor Institute, Kyoto University, 2-1010, Asashiro-nishi, Kumatori-cho, Sennan-gun, Osaka 590-0494, Japan.
World J Oncol. 2014 Aug;5(4):155-165. doi: 10.14740/wjon855w. Epub 2014 Aug 25.
The aim of this study was to evaluate the significance of fractionated administration of thalidomide combined with γ-ray irradiation in terms of local tumor response and lung metastatic potential, referring to the response of intratumor quiescent (Q) cells.
B16-BL6 melanoma tumor-bearing C57BL/6 mice were continuously given 5-bromo-2'-deoxyuridine (BrdU) to label all proliferating (P) cells. The tumor-bearing mice then received γ-ray irradiation after thalidomide treatment through a single or two consecutive daily intraperitoneal administrations up to a total dose of 400 mg/kg in combination with an acute hypoxia-releasing agent (nicotinamide) or mild temperature hyperthermia (MTH). Immediately after the irradiation, cells from some tumors were isolated and incubated with a cytokinesis blocker. The responses of the Q and total (= P + Q) cell populations were assessed based on the frequency of micronuclei using immunofluorescence staining for BrdU. In other tumor-bearing mice, 17 days after irradiation, macroscopic lung metastases were enumerated.
Thalidomide raised the sensitivity of the total cell population more remarkably than Q cells in both single and daily administrations. Daily administration of thalidomide elevated the sensitivity of both the total and Q cell populations, but especially the total cell population, compared with single administration. Daily administration, especially combined with MTH, decreased the number of lung metastases.
Daily fractionated administration of thalidomide in combination with γ-ray irradiation was thought to be more promising than single administration because of its potential to enhance local tumor response and repress lung metastatic potential.
本研究旨在通过参考肿瘤内静止(Q)细胞的反应,评估沙利度胺分次给药联合γ射线照射在局部肿瘤反应和肺转移潜能方面的意义。
给荷B16-BL6黑色素瘤的C57BL/6小鼠连续注射5-溴-2'-脱氧尿苷(BrdU)以标记所有增殖(P)细胞。荷瘤小鼠在沙利度胺治疗后接受γ射线照射,沙利度胺通过单次或连续两天腹腔注射给药,总剂量达400mg/kg,并联合急性缺氧释放剂(烟酰胺)或轻度体温热疗(MTH)。照射后立即从部分肿瘤中分离细胞,并用细胞分裂阻滞剂进行孵育。使用BrdU免疫荧光染色,基于微核频率评估Q细胞群和总细胞群(=P+Q)的反应。在其他荷瘤小鼠中,照射后17天,计数肉眼可见的肺转移灶数量。
在单次给药和每日给药中,沙利度胺提高总细胞群的敏感性比Q细胞更显著。与单次给药相比,沙利度胺每日给药提高了总细胞群和Q细胞群的敏感性,但尤其是总细胞群。每日给药,特别是联合MTH,减少了肺转移灶的数量。
沙利度胺每日分次给药联合γ射线照射被认为比单次给药更有前景,因为它有增强局部肿瘤反应和抑制肺转移潜能的潜力。