首页> 外文期刊>Urological research >Radiation induces p53-dependent cell apoptosis in bladder cancer cells with wild-type- p53 but not in p53-mutated bladder cancer cells.
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Radiation induces p53-dependent cell apoptosis in bladder cancer cells with wild-type- p53 but not in p53-mutated bladder cancer cells.

机译:辐射在具有野生型p53的膀胱癌细胞中诱导p53依赖性细胞凋亡,但在p53突变的膀胱癌细胞中不诱导。

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Purpose. It has been reported in several studies that the absence in cancer cells of the p53 tumor suppressor gene, mutations of which are frequently found in bladder cancer, increases their resistance to ionizing radiation. Other studies, however, suggest that mutations of the p53 gene could increase the radiosensitivity of cancer cells, although the evidence is still inconclusive. In the present study, we investigated the relationship between p53 status and radiation response in five different bladder cancer cell lines. Materials and Methods. Five different human bladder cancer cell lines (KK47: with wt- p53, RT4: with wt- p53, T24: with mutated p53, 5637: with mutated p53, UM-UC-3: with mutated p53) were used in the study. Cells were irradiated with 0, 2, 4, 6 or 8 Gy, then trypsinized and re-plated for clonogenic survival assay, quantitative RT-PCR assay, flow-cytometry analysis and TUNEL assay. Results. The clonogenic assay demonstrated that KK47 and RT4 had significantly higher radiosensitivity than other cell lines. Quantitative RT-PCR analysis showed that radiation induced increased expression of p53, Bax, and p21 mRNA in KK47 and RT4. After irradiation, G1 cell-cycle arrest was observed in KK47 and RT4 under flow cytometry analysis, while T24, 5637, and UM-UC-3 showed an increase in the proportion of G2 cells. Increased cell apoptosis was also observed under TUNEL assay in KK47 and RT4, but not in other cell lines. Conclusions: It was demonstrated that ionizing radiation induces p53-dependent cell apoptosis in bladder cancer cells with wt- p53 but not in those with mutated p53.
机译:目的。据几项研究报道,癌细胞中不存在p53抑癌基因,而这种突变在膀胱癌中经常发现,增加了其对电离辐射的抵抗力。然而,其他研究表明,p53基因的突变可能增加癌细胞的放射敏感性,尽管证据尚无定论。在本研究中,我们调查了5种不同的膀胱癌细胞系中p53状态与放射反应之间的关系。材料和方法。在研究中使用了五种不同的人膀胱癌细胞系(KK47:具有wt-p53,RT4:具有wt-p53,T24:具有突变的p53,5637:具有突变的p53,UM-UC-3:具有突变的p53)。用0、2、4、6或8 Gy照射细胞,然后进行胰蛋白酶消化并重新铺平板以进行克隆形成存活测定,定量RT-PCR测定,流式细胞术分析和TUNEL测定。结果。克隆形成试验表明,KK47和RT4的放射敏感性明显高于其他细胞系。 RT-PCR定量分析表明,辐射诱导KK47和RT4中p53,Bax和p21 mRNA的表达增加。照射后,在流式细胞仪分析下,在KK47和RT4中观察到G1细胞周期停滞,而T24、5637和UM-UC-3显示G2细胞比例增加。在TUNEL分析中,在KK47和RT4中也观察到细胞凋亡增加,但在其他细胞系中未观察到。结论:已证明电离辐射在具有wt-p53的膀胱癌细胞中诱导p53依赖性细胞凋亡,而在具有突变的p53的细胞中不诱导凋亡。

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