Johansson Veronica M, Miniotis Maria Falck, Hegardt Cecilia, Jönsson Göran, Staaf Johan, Berntsson Pia S H, Oredsson Stina M, Alm Kersti
Department of Cell and Organism Biology, Lund University, Helgonavägen 3B, SE-223 62 Lund, Sweden.
Cell Biol Int. 2008 Dec;32(12):1467-77. doi: 10.1016/j.cellbi.2008.08.018. Epub 2008 Aug 22.
Polyamine depletion causes S phase prolongation, and earlier studies indicate that the elongation step of DNA replication is affected. This led us to investigate the effects of polyamine depletion on enzymes crucial for Okazaki fragment maturation in the two breast cancer cell lines MCF-7 and L56Br-C1. In MCF-7 cells, treatment with N(1),N(11)-diethylnorspermine (DENSPM) causes S phase prolongation. In L56Br-C1 cells the prolongation is followed by massive apoptosis. In the present study we show that L56Br-C1 cells have substantially lower basal expressions of two Okazaki fragment maturation key proteins, DNA ligase I and FEN1, than MCF-7 cells. Thus, these two proteins might be promising markers for prediction of polyamine depletion sensitivity, something that can be useful for cancer treatment with polyamine analogues. DENSPM treatment affects the cellular distribution of FEN1 in L56Br-C1 cells, but not in MCF-7 cells, implying that FEN1 is affected by or involved in DENSPM-induced apoptosis.
多胺耗竭会导致S期延长,早期研究表明DNA复制的延伸步骤受到影响。这促使我们研究多胺耗竭对两种乳腺癌细胞系MCF-7和L56Br-C1中冈崎片段成熟至关重要的酶的影响。在MCF-7细胞中,用N(1),N(11)-二乙基亚精胺(DENSPM)处理会导致S期延长。在L56Br-C1细胞中,延长之后会出现大量细胞凋亡。在本研究中,我们表明L56Br-C1细胞中两种冈崎片段成熟关键蛋白DNA连接酶I和FEN1的基础表达水平明显低于MCF-7细胞。因此,这两种蛋白可能是预测多胺耗竭敏感性的有前景的标志物,这对于用多胺类似物进行癌症治疗可能有用。DENSPM处理会影响L56Br-C1细胞中FEN1的细胞分布,但不影响MCF-7细胞中的分布,这意味着FEN1受DENSPM诱导的细胞凋亡影响或参与其中。