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
相关论文
共 31 条
  • [1] ALEXANDROVA N, 1995, MOL CELL BIOL, V15, P5188
  • [2] AVIGAN MI, 1990, J BIOL CHEM, V265, P18538
  • [3] BHALLA K, 1993, LEUKEMIA, V7, P563
  • [4] APOPTOTIC CELL-DEATH INDUCED BY C-MYC IS INHIBITED BY BCL-2
    BISSONNETTE, RP
    ECHEVERRI, F
    MAHBOUBI, A
    GREEN, DR
    [J]. NATURE, 1992, 359 (6395) : 552 - 554
  • [5] TAXOL, A MICROTUBULE-STABILIZING ANTINEOPLASTIC AGENT, INDUCES EXPRESSION OF TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-1 IN MACROPHAGES
    BOGDAN, C
    DING, A
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1992, 52 (01) : 119 - 121
  • [6] BURKHART CA, 1994, CANCER RES, V54, P5779
  • [7] Differentiation of human colon cancer cells changes the expression of β-tubulin isotypes and MAPs
    Carles, G
    Braguer, D
    Dumontet, C
    Bourgarel, V
    Gonçalves, A
    Sarrazin, M
    Rognoni, JB
    Briand, C
    [J]. BRITISH JOURNAL OF CANCER, 1999, 80 (08) : 1162 - 1168
  • [8] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [9] I kappa B alpha physically interacts with a cytoskeleton-associated protein through its signal response domain
    Crepieux, P
    Kwon, H
    Leclerc, N
    Spencer, W
    Richard, S
    Lin, RT
    Hiscott, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (12) : 7375 - 7385
  • [10] EVIDENCE THAT MICROTUBULE DEPOLYMERIZATION EARLY IN THE CELL-CYCLE IS SUFFICIENT TO INITIATE DNA-SYNTHESIS
    CROSSIN, KL
    CARNEY, DH
    [J]. CELL, 1981, 23 (01) : 61 - 71