Regulation of the p14ARF-Mdm2-p53 pathway: An overview in breast cancer

被引:81
作者
Agrawal, Anshu [1 ]
Yang, Jianhui [1 ]
Murphy, Richard F. [1 ]
Agrawal, Devendra K. [1 ]
机构
[1] Creighton Univ, Sch Med, Dept Biomed Sci Med & Med Microbiol & Immunol, Omaha, NE 68178 USA
关键词
D O I
10.1016/j.yexmp.2006.07.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Knowledge of the roles of proteins that are abnormally suppressed or activated due to mutation in the DNA sequences of the common tumor suppressor genes, p14ARF and p53, is critical to the understanding the pathogenesis of breast cancer. Mdm2 is a mediator for the function of both p14ARF and p53. In this review article factors including Pokemon, Geminin, Twist, and Apigenin, which control the action of individual proteins in the p14ARF-Mdm2-p53 pathway in breast cancer as well the consequences of mutation 7 of p53 are discussed. The complexity of interaction of components of the pathway and the underlying development of cancer is emphasized. Opportunities for future therapeutic innovations are indicated. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
相关论文
共 117 条
[1]   Global trends in breast cancer incidence and mortality 1973-1997 [J].
Althuis, MD ;
Dozier, JM ;
Anderson, WF ;
Devesa, SS ;
Brinton, LA .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2005, 34 (02) :405-412
[2]   Relationship between the expression of various markers and prognostic factors in breast cancer [J].
Anim, JT ;
John, B ;
Abdulsathar, SA ;
Prasad, A ;
Saji, T ;
Akhtar, N ;
Ali, V ;
Al-Saleh, M .
ACTA HISTOCHEMICA, 2005, 107 (02) :87-93
[3]   MOLECULAR AND CELLULAR ANALYSIS OF BASEMENT-MEMBRANE INVASION BY HUMAN BREAST-CANCER CELLS IN MATRIGEL-BASED INVITRO ASSAYS [J].
BAE, SN ;
ARAND, G ;
AZZAM, H ;
PAVASANT, P ;
TORRI, J ;
FRANDSEN, TL ;
THOMPSON, EW .
BREAST CANCER RESEARCH AND TREATMENT, 1993, 24 (03) :241-255
[4]  
BARTEK J, 1990, ONCOGENE, V5, P893
[5]   Centrosome hyperamplification in human cancer: chromosome instability induced by p53 mutation and/or Mdm2 overexpression [J].
Carroll, PE ;
Okuda, M ;
Horn, HF ;
Biddinger, P ;
Stambrook, PJ ;
Gleich, LL ;
Li, YQ ;
Tarapore, P ;
Fukasawa, K .
ONCOGENE, 1999, 18 (11) :1935-1944
[6]   Activation of p53 by MDM2 antagonists can protect proliferating cells from mitotic inhibitors [J].
Carvajal, D ;
Tovar, C ;
Yang, H ;
Vu, BT ;
Heimbrook, DC ;
Vassilev, LT .
CANCER RESEARCH, 2005, 65 (05) :1918-1924
[7]   Inhibiting the p53-MDM2 interaction:: An important target for cancer therapy [J].
Chène, P .
NATURE REVIEWS CANCER, 2003, 3 (02) :102-109
[8]   Prognostic and predictive factors in early-stage breast cancer [J].
Cianfrocca, M ;
Goldstein, LJ .
ONCOLOGIST, 2004, 9 (06) :606-616
[9]  
Dang JJ, 2002, CANCER RES, V62, P1222
[10]   p53 mutation as a genetic trait of typical medullary breast carcinoma [J].
de Cremoux, P ;
Salomon, AV ;
Liva, S ;
Dendale, R ;
Bouchind'homme, B ;
Martin, E ;
Sastre-Garau, X ;
Magdelenat, H ;
Fourquet, A ;
Soussi, T .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (07) :641-643