Zheng A, Castren K, Säily M, Savolainen E R, Koistinen P, Vähäkangas K
Department of Clinical Chemistry, University of Oulu, Finland.
Br J Cancer. 1999 Feb;79(3-4):407-15. doi: 10.1038/sj.bjc.6690064.
We analysed the status of the p53 gene and protein in eight newly established acute myeloid leukaemia (AML) cell lines representing blast cells of either de novo leukaemia patients in first remission or patients with relapsed and chemotherapy-resistant disease causing their death. There were no mutations in the p53 gene in any of the cell lines as analysed by single-strand conformation polymorphism of amplified exons 5-8. However, the p53 protein was clearly and consistently expressed in all of these cell lines, as shown by immunohistochemistry, Western blotting and flow cytometry. The consistently expressed p53 protein was located in both the nucleus and the cytoplasm of all the cell lines and, as shown by flow cytometry, it was mostly in a conformation typical of the mutated protein. These AML cell lines offer a tool for studying the production and function of the p53 protein and its possible role in cell cycle regulation and chemoresistance as well as in the regulation of apoptosis in AML.
我们分析了8种新建立的急性髓系白血病(AML)细胞系中p53基因和蛋白的状态,这些细胞系代表初治缓解期的初发性白血病患者或复发且化疗耐药导致死亡的患者的原始细胞。通过对扩增的外显子5-8进行单链构象多态性分析,在任何细胞系中均未发现p53基因的突变。然而,免疫组织化学、蛋白质印迹法和流式细胞术显示,p53蛋白在所有这些细胞系中均有清晰且持续的表达。持续表达的p53蛋白位于所有细胞系的细胞核和细胞质中,流式细胞术显示,其大多呈突变蛋白的典型构象。这些AML细胞系为研究p53蛋白的产生和功能及其在AML细胞周期调控、化疗耐药以及细胞凋亡调控中的可能作用提供了一个工具。