THE P53-BINDING PROTEIN MDM2 GENE IS DIFFERENTIALLY EXPRESSED IN HUMAN BREAST-CARCINOMA

被引:1
|
作者
SHEIKH, MS
SHAO, ZM
HUSSAIN, A
FONTANA, JA
机构
[1] UNIV MARYLAND,SCH MED,CTR CANC,DEPT MED,DIV ONCOL,RM S9D05,22 S GREENE ST,BALTIMORE,MD 21201
[2] DEPT VET AFFAIRS MED CTR,BALTIMORE,MD 21201
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human p53-binding protein murine double minute 2 (MDM2) is believed to function as a negative regulator of p53. The MDM2 gene was cloned and sequenced only recently and was found to be amplified in a variety of sarcomas. Although mutations in the p53 gene have been shown to occur in human breast carcinoma (HBC), no information is available on MDM2 gene expression in HBC. In this study we report for the first time that the MDM2 gene is differentially expressed in HBC. Our results demonstrate a correlation between the estrogen receptor (ER) status and the MDM2 mRNA levels. In contrast to the ER-negative cell lines, all the ER-positive cell lines were found to express higher levels of MDM2 mRNA. ER-positive ZR-75 cells express 30-fold higher levels of MDM2 mRNA than does the ER-negative cell line Hs578T. Estrogen enhanced albeit modestly the MDM2 mRNA levels in ER-positive MCF-7 cells. Estrogen enhancement of MDM2 mRNA levels was also observed in ER-negative MDA-MB-231 cells transfected with functional ERs. Our data thus suggest that estrogen may play an important role in HBC growth stimulation by modulating the expression of MDM2, which in turn may inactivate the p53 function.
引用
收藏
页码:3226 / 3228
页数:3
相关论文
共 50 条
  • [31] P53 AND MDM2 ARE EXPRESSED INDEPENDENTLY DURING CELLULAR PROLIFERATION
    MOSNER, J
    DEPPERT, W
    ONCOGENE, 1994, 9 (11) : 3321 - 3328
  • [32] Inhibition of p53 DNA Binding Function by the MDM2 Protein Acidic Domain
    Cross, Brittany
    Chen, Lihong
    Cheng, Qian
    Li, Baozong
    Yuan, Zhi-Min
    Chen, Jiandong
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (18) : 16018 - 16029
  • [33] p53 inhibition by MDM2 in human pterygium
    Cao, Di
    Tsz Kin Ng
    Yip, Yolanda W. Y.
    Young, Alvin L.
    Pang, Chi Pui
    Chu, Wai Kit
    Jhanji, Vishal
    EXPERIMENTAL EYE RESEARCH, 2018, 175 : 142 - 147
  • [34] Correction: The topoisomerase I- and p53-binding protein topors is differentially expressed in normal and malignant human tissues and may function as a tumor suppressor
    Ahamed Saleem
    Jayeeta Dutta
    Diptee Malegaonkar
    Farheena Rasheed
    Zeshaan Rasheed
    Rajeev Rajendra
    Henderson Marshall
    Minjie Luo
    Honghua Li
    Eric H Rubin
    Oncogene, 2019, 38 : 6322 - 6322
  • [35] The Effect of p53 Mutations on Binding to the Mdm2 Promoter
    Morin-Gaona, Cassandra
    Nogaj, Luiza
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2024, 300 (03) : S654 - S654
  • [36] Subcellular distribution of p53 and p73 are differentially regulated by MDM2
    Gu, JJ
    Nie, LH
    Kawai, H
    Yuan, ZM
    CANCER RESEARCH, 2001, 61 (18) : 6703 - 6707
  • [37] MDM2 overexpression with alteration of the p53 protein and gene status in oral carcinogenesis
    Li, XJ
    Murai, M
    Koyama, T
    Li, XJ
    Wang, DY
    Hashimoto, K
    JAPANESE JOURNAL OF CANCER RESEARCH, 2000, 91 (05): : 492 - 498
  • [38] Elevated MDM2 contributes to antitumor activity of p53-MDM2 binding inhibitors
    Xia, Mingxuan
    Knezevic, Dejan
    Tovar, Christian
    Heimbrook, David C.
    Vassilev, Lyubomir T.
    MOLECULAR CANCER THERAPEUTICS, 2007, 6 (12) : 3616S - 3616S
  • [39] Ribosomal protein S7 as a novel modulator of p53-MDM2 interaction: binding to MDM2, stabilization of p53 protein, and activation of p53 function
    Chen, D.
    Zhang, Z.
    Li, M.
    Wang, W.
    Li, Y.
    Rayburn, E. R.
    Hill, D. L.
    Wang, H.
    Zhang, R.
    ONCOGENE, 2007, 26 (35) : 5029 - 5037
  • [40] mdm2 gene expression in primary hepatocellular carcinoma and its relationship to p53 gene mutation
    孙宝华
    武忠弼
    阮幼冰
    杨木兰
    中华医学杂志(英文版), 1998, (11) : 53 - 53