Cheng Chun-Yuan, Lin Yi-Hsiang, Su Chin-Cheng
Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan, R.O.C.
Mol Med Rep. 2010 Jan-Feb;3(1):63-7. doi: 10.3892/mmr_00000219.
Sann-Joong-Kuey-Jian-Tang (SJKJT), a traditional Chinese medicine prescription, has been used to treat lymph node diseases and tumors. However, the molecular mechanisms of SJKJT in human colon cancer in vivo and in vitro have not been clearly elucidated. In the present study, we investigated the molecular mechanisms of SJKJT in human colon cancer colo 205 cells in vitro and in vivo. In the in vitro study, colo 205 cells were treated with various concentrations (0.5, 1 and 2 mg/ml) of SJKJT. The protein expression of TNF-α, Caspase-8 and Caspase-3 in colo 205 cells was measured by Western blotting. The results demonstrate that SJKJT up-regulated Fas, TNF-α, Caspase-8 and Caspase-3 protein expression. In the in vivo study, human colon cancer colo 205 cells (3x106/0.2 ml) were injected subcutaneously into the flank area of nude SCID mice (n=32) randomly divided into four groups. SJKJT was dissolved in saline and then administered orally to the mice at concentrations of 0.01, 0.1 and 0.3 g/kg/day for 30 days. The control group was treated with an equal volume of saline. SCID mice were sacrified by CO2 inhalation and the xenograft tumors were dissected. Subsequently, the protein expression of Fas, TNF-α, Caspase-8 and Caspase-3 in the tumors was measured by Western blotting. The results demonstrate that SJKJT up-regulated Fas, TNF-α, Caspase-8 and Caspase-3 protein expression, both in vitro and in vivo. These observations suggest that SJKJT has therapeutic potential in colon cancer.
三逐瘀煎(Sann-Joong-Kuey-Jian-Tang,SJKJT)是一种中药方剂,已被用于治疗淋巴结疾病和肿瘤。然而,SJKJT在人结肠癌体内和体外的分子机制尚未完全阐明。在本研究中,我们调查了SJKJT在人结肠癌colo 205细胞体内和体外的分子机制。在体外研究中,用不同浓度(0.5、1和2 mg/ml)的SJKJT处理colo 205细胞。通过蛋白质印迹法检测colo 205细胞中TNF-α、Caspase-8和Caspase-3的蛋白质表达。结果表明,SJKJT上调了Fas、TNF-α、Caspase-8和Caspase-3的蛋白质表达。在体内研究中,将人结肠癌colo 205细胞(3×106/0.2 ml)皮下注射到随机分为四组的裸SCID小鼠(n = 32)的侧腹区域。将SJKJT溶解在盐水中,然后以0.01、0.1和0.3 g/kg/天的浓度口服给药小鼠30天。对照组用等体积的盐水处理。通过吸入CO2处死SCID小鼠并解剖异种移植肿瘤。随后,通过蛋白质印迹法测量肿瘤中Fas、TNF-α、Caspase-8和Caspase-3的蛋白质表达。结果表明,SJKJT在体外和体内均上调了Fas、TNF-α、Caspase-8和Caspase-3的蛋白质表达。这些观察结果表明,SJKJT在结肠癌中具有治疗潜力。