McIntyre L J, Kim Y S
Eur J Cancer Clin Oncol. 1984 Feb;20(2):265-71. doi: 10.1016/0277-5379(84)90194-9.
The effects of 1 mM sodium butyrate or 2% dimethylsulfoxide (DMSO) on three human pancreatic tumor cell lines were examined. The cell lines tested were MIA PaCa-2, PANC-1 and CAPAN-1. Both butyrate and DMSO inhibited the ability of all three lines to form colonies in soft agar. These results suggest that the use of these agents provides a model system for the study of the molecular changes involved in human pancreatic cancer. In butyrate all the cell lines showed a marked increase in cellular levels of alkaline phosphatase, while growth in DMSO led to a reduction in most cases. DMSO caused a rapid reduction in the attachment of all three cell lines to collagen substrates, while butyrate had no effect. These results illustrate the fact that although both butyrate and DMSO appear to greatly reduce the parameters correlated with tumorigenicity of human pancreatic cancer cells, the mechanisms involved may be very different.
研究了1 mM丁酸钠或2%二甲基亚砜(DMSO)对三种人胰腺肿瘤细胞系的影响。所测试的细胞系为MIA PaCa-2、PANC-1和CAPAN-1。丁酸钠和DMSO均抑制了这三种细胞系在软琼脂中形成集落的能力。这些结果表明,使用这些试剂为研究人类胰腺癌所涉及的分子变化提供了一个模型系统。在丁酸钠作用下,所有细胞系的细胞碱性磷酸酶水平均显著升高,而在DMSO中生长在大多数情况下导致降低。DMSO导致所有三种细胞系与胶原底物的附着迅速减少,而丁酸钠没有影响。这些结果说明了这样一个事实,即尽管丁酸钠和DMSO似乎都能大大降低与人类胰腺癌细胞致瘤性相关的参数,但所涉及的机制可能非常不同。