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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >The effect of Wortmannin on radiation-induced chromosome aberration formation in the radioresistant tumor cell line WiDr
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The effect of Wortmannin on radiation-induced chromosome aberration formation in the radioresistant tumor cell line WiDr

机译:渥曼青霉素对放射线诱导的肿瘤细胞系WiDr中辐射诱导的染色体畸变形成的影响

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摘要

We analyzed the formation of radiation-induced chromosome aberrations in the cells of the radioresistant colon carcinoma cell line WiDr after treatment with wortmannin, an inhibitor of PI-3 kinases, including DNA-PK. Cells irradiated in G(0)/G(1) phase with 200 kV X rays were treated with wortmannin before or after irradiation. Chromosome-type and chromatid-type aberrations were scored in metaphase cells by either Giemsa staining or FISH. Moreover, DNA-PK activity was measured in the absence and presence of wortmannin. In irradiated G(0)/G(1)-phase WiDr cells, only chromosome-type aberrations, including simple and complex exchanges and excess acentrics, were observed. After addition of 1 to 20 mu M wortmannin, the formation of chromosome-type exchange aberrations was completely suppressed. The irradiated cells displayed exclusively chromatid-type aberrations including simple and complex chromatid exchanges and chromatid/isochromatid breaks. Whether the chromatid-type aberrations arise during G(0)/G(1) as a result of homologous recombination processes coping with damaged DNA or whether DNA damage induced during G(0)/G(1) phase persists until S and G(2) phase and is then processed by homologous recombination pathways must be investigated further. (c) 2005 by Radiation Research Society.
机译:我们分析了用渥曼青霉素(一种包括DNA-PK的PI-3激酶的抑制剂)处理后,在辐射抗性结肠癌细胞系WiDr的细胞中放射诱导的染色体畸变的形成。在照射之前或之后,用渥曼青霉素处理在200 kV X射线的G(0)/ G(1)相中照射的细胞。通过Giemsa染色或FISH在中期细胞中对染色体型和染色单体型畸变进行评分。此外,在不存在渥曼青霉素的情况下测量DNA-PK活性。在辐照的G(0)/ G(1)相WiDr细胞中,仅观察到染色体类型的畸变,包括简单和复杂的交换以及多余的无心轴。加入1至20μM渥曼青霉素后,染色体型交换畸变的形成被完全抑制。受辐照的细胞仅显示染色单体类型的像差,包括简单和复杂的染色单体交换和染色单体/同染色单体断裂。是由于同源重组过程应对受损的DNA而导致在G(0)/ G(1)期间发生了染色单体型畸变,还是在G(0)/ G(1)阶段诱导的DNA损伤一直持续到S和G( 2)阶段,然后通过同源重组途径进行加工,必须进一步研究。 (c)辐射研究学会,2005年。

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