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DDP-induced cytotoxicity is not influenced by p53 in nine human ovarian cancer cell lines with different p53 status.

机译:DDP诱导的细胞毒性不受p53状态不同的九种人类卵巢癌细胞系中p53的影响。

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摘要

Nine human ovarian cancer cell lines that express wild-type (wt) or mutated (mut) p53 were used to evaluate the cytotoxicity induced by cisplatin (DDP). The concentrations inhibiting the growth by 50% (IC50) were calculated for each cell line, and no differences were found between cells expressing wt p53 and mut p53. Using, for each cell line, the DDP IC50, we found that these concentrations were able to induce an increase in p53 levels in all four wt-p53-expressing cell lines and in one out of five mut-p53-expressing cell lines. WAF1 and GADD45 mRNAs were also increased by DDP treatment, independently of the presence of a wt p53. Bax levels were only marginally affected by DDP, and this was observed in both wt-p53- and mut-p53-expressing cells. DDP-induced apoptosis was evident 72 h after treatment, and the percentage of cells undergoing apoptosis was slightly higher for wt-p53-expressing cells. However, at doses near the IC50, the percentage of apoptotic cells was less than 20% in all the cell lines investigated. We conclude that the presence of wt p53 is not a determinant for the cytotoxicity induced by DDP in human ovarian cancer cell lines.
机译:表达野生型(wt)或突变(mut)p53的九种人类卵巢癌细胞系用于评估顺铂(DDP)诱导的细胞毒性。计算每种细胞系抑制生长50%的浓度(IC50),在表达wt p53和mut p53的细胞之间未发现差异。对于每种细胞系,使用DDP IC50,我们发现这些浓度能够诱导所有四个表达wt-p53的细胞系和五个表达mut-p53的细胞系之一中p53水平的增加。通过DDP处理,WAF1和GADD45 mRNA也增加,与wt p53的存在无关。 Bax水平仅受DDP轻微影响,这在表达wt-p53和mut-p53的细胞中均可观察到。 DDP诱导的细胞凋亡在处理后72小时明显,并且表达wt-p53的细胞经历细胞凋亡的百分比略高。但是,在接近IC50的剂量下,所有研究的细胞系中凋亡细胞的百分比均小于20%。我们得出结论,wt p53的存在不是人类卵巢癌细胞系中DDP诱导的细胞毒性的决定因素。

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