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γ-H2AX 焦点的衰减与前列腺癌细胞中潜在致死性损伤修复相关。

Decay of γ-H2AX foci correlates with potentially lethal damage repair in prostate cancer cells.

机构信息

Department of Radiation Oncology, Laboratory for Experimental Oncology and Radiobiology (LEXOR), Center for Experimental Molecular Medicine, Academic Medical Center, University of Amsterdam, and Free University Hospital, Amsterdam, The Netherlands.

出版信息

Oncol Rep. 2013 Jun;29(6):2175-80. doi: 10.3892/or.2013.2364. Epub 2013 Mar 26.

Abstract

To determine the relationship between ionizing radiation-induced levels of γ-H2AX foci and cell survival in cultured prostate cancer cell lines, three prostate cancer cell lines: LNCaP (wt TP53), DU145 (mut TP53) and PC3 (TP53 null), were studied. For γ-H2AX foci induction, cells were irradiated with a single dose of 2 Gy and foci levels were studied at 30 min and 24 h after irradiation. Cell survival was determined by clonogenic assay, directly and 24 h after irradiation with doses ranging from 0 to 8 Gy. Irradiation was performed with a Siemens Stabilipan 250 KeV X-ray machine at a dose rate of approximately 3 Gy/min. Survival curves were analyzed using the linear-quadratic model S(D)/S(0)=exp-(αD+βD2). LNCaP cells clearly demonstrated potentially lethal damage repair (PLDR) which was assessed as increased survival levels after delayed plating as compared to cells plated immediately after irradiation. DU145 cells demonstrated only a slight PLDR and PC3 cells did not show PLDR at all. Levels of γ-H2AX foci were significantly decreased in all cell lines at 24 h after irradiation, compared to levels after 30 min. The LNCaP cells which demonstrated a clear PLDR also showed the largest decay in the number of γ-H2AX foci. In addition, the PC cells which did not show PLDR had the lowest decay of γ-H2AX foci. A clear correlation was demonstrated between the degree of decay of γ-H2AX foci and PLDR.

摘要

为了确定电离辐射诱导的 γ-H2AX 焦点水平与培养的前列腺癌细胞系中细胞存活之间的关系,研究了三种前列腺癌细胞系:LNCaP(wt TP53)、DU145(mut TP53)和 PC3(TP53 缺失)。对于 γ-H2AX 焦点诱导,用 2 Gy 的单次剂量照射细胞,并在照射后 30 分钟和 24 小时研究焦点水平。细胞存活通过克隆形成测定法直接测定,并且在 0 至 8 Gy 的剂量下照射后 24 小时测定。用西门子 Stabilipan 250 KeV X 射线机在约 3 Gy/min 的剂量率下进行照射。使用线性二次模型 S(D)/S(0)=exp-(αD+βD2)分析生存曲线。LNCaP 细胞明显显示出潜在致死性损伤修复(PLDR),与照射后立即接种的细胞相比,延迟接种的细胞存活水平增加,从而评估出 PLDR。DU145 细胞仅显示出轻微的 PLDR,而 PC3 细胞根本没有显示 PLDR。与照射后 30 分钟相比,照射后 24 小时,所有细胞系中的 γ-H2AX 焦点水平均明显降低。显示出明显 PLDR 的 LNCaP 细胞的 γ-H2AX 焦点数量下降也最大。此外,未显示 PLDR 的 PC 细胞的 γ-H2AX 焦点下降幅度最低。γ-H2AX 焦点衰减程度与 PLDR 之间显示出明显的相关性。

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