Opposite effects of antimicrotubule agents on c-myc oncogene expression depending on the cell lines used

被引:17
作者
Bourgarel-Rey, V
El Khyari, S
Rimet, O
Bordas, B
Guigal, N
Braguer, D
Seree, E
Barra, Y
Briand, C
机构
[1] Fac Pharm, CNRS, UPRES A 6032, F-13005 Marseille, France
[2] Univ Chouaib Doukkali, Lab Microbiol & Biotechnol, El Jadida, Morocco
关键词
antimicrotubule agents; c-myc; transcription activation;
D O I
10.1016/S0959-8049(00)00042-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the expression of c-myc in HT29-D4, HBL100 and Caco-2 cells treated with microtubule stabilising (paclitaxel) or depolymerising agents (Vinblastine, nocodazole). After induction by epidermal growth factor (EGF), c-myc expression decreased in HT29-D4 cells treated with all the antimicrotubule agents. In HBL100 and Caco-2, when microtubules were stabilised with paclitaxel, c-myc expression also decreased. In contrast, its expression increased after treatment with depolymerising agents. In both cell lines, we also observed that depolymerising agents alone induced c-myc expression whilst paclitaxel had no effect. This mRNA induction was confirmed at the protein level. In HT29-D4, no Variation of c-myc expression was observed. Then, we showed that the increase of mRNA level was due to activation of gene transcription. These results indicate that modulation of c-myc expression varied depending on the cell lines used and the type of antimicrotubule agents. This work provides a potential link between the microtubular network and c-myc gene expression. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1043 / 1049
页数:7
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