Vikhanskaya F, Colella G, Valenti M, Parodi S, D'Incalci M, Broggini M
Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri via Eritrea, Milan, Italy.
Clin Cancer Res. 1999 Apr;5(4):937-41.
We have studied the possible interactions between the mismatch repair system and p53 in a human colon cancer cell line, HCT-116 (known to have a homozygous mutation in mismatch repair gene hMLH1 on chromosome 3) and in a clone obtained after insertion of a single copy of chromosome 3 (HCT-116+ ch3). Loss of DNA mismatch repair activity resulted in resistance to cisplatin (DDP). p53 accumulated differently in these cell lines after treatment with DDP. Initially at similar high levels after DDP treatment, p53 maintained the increase in HCT-116 cells, even 72-96 h after drug exposure, whereas HCT-116+ch3 mismatch-proficient cell line p53 declined to basal levels after 48 h. The higher levels of p53 in mismatch-deficient HCT-116 cells were accompanied by increased transcriptional activity as assessed by the gel-retardation assay and by activation of a promoter containing a p53 DNA binding site. To better understand the role of p53, if any, in cell sensitivity to DDP, we disrupted p53 in both cell lines by stable transfection with the human papillomavirus type 16 E6 gene. HCT-116/E6 cells were more sensitive to DDP than the parental cell line, whereas HCT-116+ch3/E6 were fairly similar to HCT-116+ch3 with normal p53 function. Although in our system the transfer of the entire chromosome 3 was used (thus not excluding a possible role of other genes localized on this chromosome), our data indicate that p53 can cooperate with the mismatch repair system. In fact, the lack of hLMH1, at least in these cells, enhances the role of p53 in protecting the cells from DDP-induced DNA damage.
我们研究了错配修复系统与p53在人结肠癌细胞系HCT-116(已知在3号染色体上的错配修复基因hMLH1存在纯合突变)以及在插入单拷贝3号染色体后获得的克隆(HCT-116+ch3)中的可能相互作用。DNA错配修复活性的丧失导致对顺铂(DDP)的抗性。用DDP处理后,p53在这些细胞系中的积累情况不同。DDP处理后最初p53水平相似且较高,p53在HCT-116细胞中持续增加,甚至在药物暴露后72 - 96小时仍保持,而错配修复功能正常的HCT-116+ch3细胞系中p53在48小时后降至基础水平。通过凝胶阻滞试验评估,错配缺陷的HCT-116细胞中较高水平的p53伴随着转录活性增加,并且含有p53 DNA结合位点的启动子被激活。为了更好地理解p53在细胞对DDP敏感性中的作用(如果有),我们通过用16型人乳头瘤病毒E6基因稳定转染在两个细胞系中破坏p53。HCT-116/E6细胞比亲代细胞系对DDP更敏感,而HCT-116+ch3/E6与具有正常p53功能的HCT-116+ch3相当相似。尽管在我们的系统中使用了整个3号染色体的转移(因此不排除位于该染色体上的其他基因的可能作用),但我们的数据表明p53可以与错配修复系统协同作用。事实上,至少在这些细胞中,hLMH1的缺失增强了p53在保护细胞免受DDP诱导的DNA损伤中的作用。