Sakurai Noritaka, Suzuki Kazuyuki, Sano Yuki, Saito Teruyoshi, Yoshimura Hisashi, Nishimura Yukie, Yano Tomohiro, Sadzuka Yasuyuki, Asano Ryuji
Department of Veterinary Medicine, College of Bioresource Sciences, Nihon University, Kanagawa 252-8510, Japan.
Mol Med Rep. 2008 Nov-Dec;1(6):903-7. doi: 10.3892/mmr_00000048.
The present study was designed to investigate the effects of Bowman-Birk inhibitor concentrate (BBIC) on anti-proliferation, up-regulation of Connexin 43 (Cx43) expression and inhabitation of hepatic metastasis in mice with M5076 ovarian sarcoma. M5076 ovarian sarcomas (1x106 cells/animal) were subcutaneously transplanted into the back of BDF1 mice. The 'pre-treated' (n=10) and 'post-treated' (n=10) groups were fed a standard diet (CE-2) compounded with 0.5% BBI from 3 weeks before and from the day of tumor inoculation, respectively, until 4 weeks after tumor inoculation. The 'control group' (n=10) was fed CE-2 alone. Relative tumor weights in the pre- (0.013±0.010) and post- (0.012±0.013) treated groups were significantly reduced by 30.0 and 32.5%, respectively, as compared to the control group (0.040±0.022, p<0.01). The relative densities of Cx43 mRNA and Cx43 protein were significantly higher in the BBIC-treated groups than in the control group. The median numbers of macroscopic spontaneous metastases were significantly lower in the pre- (1.0±2.3) and post- (1.9±3.6) treated groups than in the control group (71.4±97.3). These results suggest that BBIC reduces proliferation as a result of increased expression of Cx43 genes in mice with M5076 ovarian sarcoma. In addition, BBIC inhibits hepatic metastasis in M5076-bearing mice.
本研究旨在探讨鲍曼-伯克抑制剂浓缩物(BBIC)对M5076卵巢肉瘤小鼠的抗增殖作用、连接蛋白43(Cx43)表达上调及肝转移抑制作用。将M5076卵巢肉瘤(1×10⁶个细胞/只动物)皮下移植到BDF1小鼠背部。“预处理”组(n = 10)和“后处理”组(n = 10)分别在肿瘤接种前3周和接种当天开始喂食添加0.5% BBI的标准饮食(CE - 2),直至肿瘤接种后4周。“对照组”(n = 10)仅喂食CE - 2。与对照组(0.040±0.022,p<0.01)相比,预处理组(0.013±0.010)和后处理组(0.012±0.013)的相对肿瘤重量分别显著降低了30.0%和32.5%。BBIC处理组中Cx43 mRNA和Cx43蛋白的相对密度显著高于对照组。预处理组(1.0±2.3)和后处理组(1.9±3.6)的肉眼可见自发转移中位数显著低于对照组(71.4±97.3)。这些结果表明,BBIC通过增加M5076卵巢肉瘤小鼠Cx43基因的表达来降低增殖。此外,BBIC可抑制荷M5076小鼠的肝转移。