Cell differentiation and chemotherapy influence p53 and Mdm2 immunoreactivity in human HT29 colon cancer cells grown in scid mice

被引:17
作者
Schumacher, U
Adam, E
Feldhaus, S
Katoh, M
Lane, DP
机构
[1] Univ Hamburg, Krankenhaus Eppendorf, Inst Anat, D-20246 Hamburg, Germany
[2] Univ Southampton, Southampton SO17 1RE, Hants, England
[3] Univ Dundee, Inst Med Sci, CRC, Cell Transformat Res Grp,Dept Biochem, Dundee DD1 4HN, Scotland
关键词
apoptosis; cell differentiation; chemotherapy; Mdm2; p53; scid mouse;
D O I
10.1016/S0304-3835(01)00395-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Absence of a functional p53 gene product can lead to increased p53 accumulation in cancer cells. In this contribution, the association between cell differentiation, chemotherapy and p53 immunoreactivity in human HT29 colon cancer cells grown in scid mice as undifferentiated cells and as mucin containing signet-ring cells was investigated. Mutated p53 was more frequently expressed in the undifferentiated tumour cells than in the signer-ring cells. 5-fluorouracil (5FU) treatment resulted in a substantial increase in the p53-positive signet-ring cell population (from 17% to 45%) and in an increased Mdm2 immunoreactivity. These findings indicate that mutated p53 expression is related to the differentiation pattern and that tumour cells devoid of mutated p53 immunoreactivity are preferentially eliminated by 5FU treatment. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:215 / 221
页数:7
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