Synergistic activation of p53 by inhibition of MDM2 expression and DNA damage

被引:158
作者
Chen, LH
Agrawal, S
Zhou, WQ
Zhang, RW
Chen, JD
机构
[1] Louisiana State Univ, Med Ctr, Dept Microbiol, Stanley S Scott Canc Ctr, New Orleans, LA 70112 USA
[2] Hybridon, Cambridge, MA 02139 USA
[3] Univ Alabama, Div Clin Pharmacol, Birmingham, AL 35291 USA
关键词
antisense oligonucleotide; oncogene; tumor suppressor;
D O I
10.1073/pnas.95.1.195
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The MDM2 oncogene encodes an inhibitor of the p53 tumor suppressor protein that regulates p53 in a negative feedback loop. MDM2 gene amplification and overexpression occur in several types of tumors and are often associated with poor prognosis. An MDM2 antisense phosphorothioate oligodeoxynucleotide has been identified that effectively inhibits MDM2 expression in tumor cells containing MDM2 gene amplifications. Antisense inhibition of MDM2 is associated with a decrease in MDM2-p53 complex formation, increase in p53-inducible gene expression, increase in p53 transcriptional activity, and apoptosis. Significantly, inhibition of MDM2 expression enhances the activation of p53 by a DNA-damaging cancer chemotherapy agent in a synergistic fashion. Therefore, the MDM2 negative feedback pathway is an important limiting factor in DNA damage-induced p53 activation. MDM2 antisense oligonucleotides may be useful as antitumor agents alone or as enhancers of other conventional DNA-damaging drugs.
引用
收藏
页码:195 / 200
页数:6
相关论文
共 40 条
  • [1] MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY
    BARAK, Y
    JUVEN, T
    HAFFNER, R
    OREN, M
    [J]. EMBO JOURNAL, 1993, 12 (02) : 461 - 468
  • [2] BENNETT CF, 1992, MOL PHARMACOL, V41, P1023
  • [3] Abnormal expression of MDM-2 in breast carcinomas
    BuesoRamos, CE
    Manshouri, T
    Haidar, MA
    Yang, Y
    McCown, P
    Ordonez, N
    Glassman, A
    Sneige, N
    Albitar, M
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 1996, 37 (02) : 179 - 188
  • [4] BUESORAMOS CE, 1993, BLOOD, V82, P2617
  • [5] CARDONCARDO C, 1994, CANCER RES, V54, P794
  • [6] INTERACTIONS BETWEEN P53 AND MDM2 IN A MAMMALIAN-CELL CYCLE CHECKPOINT PATHWAY
    CHEN, CY
    OLINER, JD
    ZHAN, QM
    FORNACE, AJ
    VOGELSTEIN, B
    KASTAN, MB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) : 2684 - 2688
  • [7] REGULATION OF TRANSCRIPTION FUNCTIONS OF THE P53 TUMOR-SUPPRESSOR BY THE MDM-2 ONCOGENE
    CHEN, JD
    LIN, JY
    LEVINE, AJ
    [J]. MOLECULAR MEDICINE, 1995, 1 (02) : 142 - 152
  • [8] Chen JD, 1996, MOL CELL BIOL, V16, P2445
  • [9] MAPPING OF THE P53 AND MDM-2 INTERACTION DOMAINS
    CHEN, JD
    MARECHAL, V
    LEVINE, AJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (07) : 4107 - 4114
  • [10] Proteolytic cleavage of the mdm2 oncoprotein during apoptosis
    Chen, LH
    Marechal, V
    Moreau, J
    Levine, AJ
    Chen, JD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) : 22966 - 22973