Ohmori Hitoshi, Sasahira Tomonori, Fujii Kiyomu, Yi Luo, Shimomoto Takasumi, Kuniyasu Hiroki
Department of Molecular Pathology, Nara Medical University School of Medicine, Kashihara, Nara, Japan.
Pathobiology. 2008;75(4):226-32. doi: 10.1159/000132383. Epub 2008 Jun 26.
We examined the effect of linoleic acid (LA) on tumor formation. Cell growth was suppressed by LA in a dose-dependent manner in MKN28 and Colo320 cells. Continuous treatment with LA provided growth arrest in both cells at 5-7 weeks after the treatment. LA-pretreated MKN28 and Colo320 cells showed higher tumorigenicity (9/10 and 10/10, respectively) than nontreated cells (2/10 and 3/10, respectively; p < 0.01) in nude mice. In contrast, LA-pretreated MKN28 and Colo320 cells showed more suppressed tumor growth than nontreated cells (p < 0.01). LA-pretreated MKN28 and Colo320 cells with LA administration after the inoculation did not form macroscopic tumors. Histological examination revealed small cancer cell aggregations, which showed no proliferative activity. In LA-treated MKN28 and Colo320 cells, protein production of Bcl-2 was increased, whereas Bak, EGFR and VEGF levels were decreased. These findings suggest that LA might induce quiescence and subsequent dormancy in cancer cells.
我们研究了亚油酸(LA)对肿瘤形成的影响。在MKN28和Colo320细胞中,LA以剂量依赖的方式抑制细胞生长。用LA持续处理在处理后5 - 7周使两种细胞均出现生长停滞。在裸鼠中,经LA预处理的MKN28和Colo320细胞比未处理的细胞表现出更高的致瘤性(分别为9/10和10/10,而未处理细胞分别为2/10和3/10;p < 0.01)。相反,经LA预处理的MKN28和Colo320细胞比未处理的细胞表现出更受抑制的肿瘤生长(p < 0.01)。接种后给予LA预处理的MKN28和Colo320细胞未形成肉眼可见的肿瘤。组织学检查显示有小的癌细胞聚集,但无增殖活性。在经LA处理的MKN28和Colo320细胞中,Bcl-2的蛋白产生增加,而Bak、EGFR和VEGF水平降低。这些发现表明LA可能诱导癌细胞进入静止状态并随后进入休眠状态。