Mori Yoko, Sahara Hiroeki, Matsumoto Kayo, Takahashi Nobuaki, Yamazaki Takayuki, Ohta Keisuke, Aoki Satoko, Miura Masahiko, Sugawara Fumio, Sakaguchi Kengo, Sato Noriyuki
Marine Biomedical Institute, Sapporo Medical University School of Medicine, S1, W17, Chuo-ku, Sapporo 060-8556, Japan.
Cancer Sci. 2008 May;99(5):1063-70. doi: 10.1111/j.1349-7006.2008.00785.x.
We previously reported that 3'-sulfoquinovosyl-1'-monoacylglycerol (SQMG) was effective in suppressing the growth of solid tumors due to hemorrhagic necrosis in vivo. In the present study, we investigated the antiangiogenic effect of SQMG. In vivo assessment of antitumor assays showed that some tumor cell lines, but not others, were sensitive to SQMG. Microscopic study suggested that in SQMG-sensitive tumors, but not SQMG-resistant tumors, angiogenesis was reduced. We next investigated gene expression relating to angiogenesis in tumor tissues by quantitative real-time polymerase chain reaction. Consequently, although vascular endothelial growth factor gene expression was not detected with significant differences among the cases, significant downregulation of Tie2 gene expression was observed in all SQMG-sensitive tumors as compared with controls, but not in SQMG-resistant tumors. These data suggested that the antitumor effects of SQMG could be attributed to antiangiogenic effects, possibly via the downregulation of Tie2 gene expression in SQMG-sensitive tumors.
我们之前报道过,3'-磺基喹诺糖基-1'-单酰甘油(SQMG)在体内可通过出血性坏死有效抑制实体瘤的生长。在本研究中,我们调查了SQMG的抗血管生成作用。体内抗肿瘤试验评估显示,一些肿瘤细胞系对SQMG敏感,而另一些则不敏感。显微镜研究表明,在对SQMG敏感的肿瘤中,而非对SQMG耐药的肿瘤中,血管生成减少。接下来,我们通过定量实时聚合酶链反应研究了肿瘤组织中与血管生成相关的基因表达。结果,虽然在各病例之间未检测到血管内皮生长因子基因表达有显著差异,但与对照组相比,在所有对SQMG敏感的肿瘤中均观察到Tie2基因表达显著下调,而在对SQMG耐药的肿瘤中则未观察到。这些数据表明,SQMG的抗肿瘤作用可能归因于抗血管生成作用,可能是通过下调对SQMG敏感肿瘤中的Tie2基因表达来实现的。