Fagot D, Buquet-Fagot C, Lallemand F, Mester J
INSERM U55, Paris, France.
Anticancer Drugs. 1994 Oct;5(5):548-56. doi: 10.1097/00001813-199410000-00006.
The proliferation of the MCF7 and MCF7-A (adriamycin-resistant) and KB-3-1 and KB-A (adriamycin-resistant) cell lines was arrested by sodium butyrate (NaBut) at 1 mM or higher concentrations. In the MCF7 and MCF7-A cell lines, an accumulation in the G1 phase was observed, whereas the KB-3-1 and KB-A cell lines accumulated in both G1 and G2/M phases. The level of the mRNA coded by the 'early G1' gene c-myc was high in all these cell lines, and was only transiently decreased by NaBut treatment. The 'late' mRNA coding for the proliferating cell nuclear antigen (PCNA) was also strongly expressed in all the cell lines studied; incubation with NaBut caused a decrease of the PCNA mRNA in the MCF7 and MCF7-A cells but not in the KB-3-1 and KB-A cells. The anti-oncoprotein p105RB was undetectable in the MCF7 and MCF7-A cells, while the KB-3-1 as well as KB-A cells contained a high level of this protein. Neither the content nor the apparent state of phosphorylation of the RB protein were affected by incubation (up to 48 h) with NaBut.
1 mM或更高浓度的丁酸钠(NaBut)可抑制MCF7和MCF7-A(阿霉素耐药)以及KB-3-1和KB-A(阿霉素耐药)细胞系的增殖。在MCF7和MCF7-A细胞系中,观察到细胞在G1期积累,而KB-3-1和KB-A细胞系在G1期和G2/M期均有积累。在所有这些细胞系中,由“早期G1”基因c-myc编码的mRNA水平都很高,并且仅在丁酸钠处理后短暂下降。编码增殖细胞核抗原(PCNA)的“晚期”mRNA在所有研究的细胞系中也强烈表达;用丁酸钠孵育导致MCF7和MCF7-A细胞中PCNA mRNA减少,但在KB-3-1和KB-A细胞中未减少。在MCF7和MCF7-A细胞中未检测到抗癌蛋白p105RB,而KB-3-1和KB-A细胞中含有高水平的这种蛋白。RB蛋白的含量和明显的磷酸化状态均不受丁酸钠孵育(长达48小时)的影响。