Institute of Molecular and Cellular Biology, Department of Life Science, Graduate Institute of Biomedical Electronics and Bioinformatics, Center for Systems Biology and Bioinformatics, Institute of Biochemical Sciences, National Taiwan University, Taiwan.
Evid Based Complement Alternat Med. 2011;2011:358717. doi: 10.1093/ecam/nep107. Epub 2011 Jan 4.
Differentiation therapy by induction of tumor cells is an important method in the treatment of hematological cancers such as leukemia. Tumor cell differentiation ends cancer cells' immortality, thus stopping cell growth and proliferation. In our previous study, we found that fucose-containing polysaccharide fraction F3 extracted from Ganoderma lucidum can bring about cytokine secretion and cell death in human leukemia THP-1 cells. This prompted us to further investigate on how F3 induces the differentiation in human leukemia cells. We integrated time-course microarray analysis and network modeling to study the F3-induced effects on THP-1 cells. In addition, we determined the differentiation effect using Liu's staining, nitroblue tetrazolium (NBT) reduction assay, flow cytometer, western blotting and Q-PCR. We also examined the modulation and regulation by F3 during the differentiation process. Dynamic gene expression profiles showed that cell differentiation was induced in F3-treated THP-1 cells. Furthermore, F3-treated THP-1 cells exhibited enhanced macrophage differentiation, as demonstrated by changes in cell adherence, cell cycle arrest, NBT reduction and expression of differentiation markers including CD11b, CD14, CD68, matrix metalloproteinase-9 and myeloperoxidase. In addition, caspase cleavage and p53 activation were found to be significantly enhanced in F3-treated THP-1 cells. We unraveled the role of caspases and p53 in F3-induced THP-1 cells differentiation into macrophages. Our results provide a molecular explanation for the differentiation effect of F3 on human leukemia THP-1 cells and offer a prospect for a potential leukemia differentiation therapy.
诱导肿瘤细胞分化是治疗白血病等血液系统癌症的重要方法。肿瘤细胞分化终止了癌细胞的永生性,从而阻止了细胞的生长和增殖。在我们之前的研究中,我们发现灵芝中提取的含岩藻糖多糖 F3 可引起人白血病 THP-1 细胞分泌细胞因子和细胞死亡。这促使我们进一步研究 F3 如何诱导人白血病细胞分化。我们整合了时间过程微阵列分析和网络建模来研究 F3 对 THP-1 细胞的诱导作用。此外,我们使用刘氏染色、硝基蓝四唑(NBT)还原测定、流式细胞仪、western blot 和 Q-PCR 来确定分化效果。我们还检查了 F3 在分化过程中的调节作用。动态基因表达谱显示,F3 处理的 THP-1 细胞中诱导了细胞分化。此外,F3 处理的 THP-1 细胞表现出增强的巨噬细胞分化,这表现在细胞黏附、细胞周期停滞、NBT 还原和分化标志物(包括 CD11b、CD14、CD68、基质金属蛋白酶-9 和髓过氧化物酶)的表达变化。此外,还发现 F3 处理的 THP-1 细胞中的半胱天冬酶裂解和 p53 激活明显增强。我们揭示了半胱天冬酶和 p53 在 F3 诱导的 THP-1 细胞向巨噬细胞分化中的作用。我们的结果为 F3 对人白血病 THP-1 细胞的分化作用提供了分子解释,并为潜在的白血病分化治疗提供了前景。