p53 in neurodegenerative diseases and brain cancers

被引:77
作者
Checler, Frederic [1 ]
da Costa, Cristine Alves [1 ]
机构
[1] UNS, CNRS, Inst Pharmacol Mol & Cellulaire, UMR7275, 660 Route Lucioles, F-06560 Valbonne, France
关键词
p53; Signaling; Alzheimer's disease; Parkinson's disease; Cerebral cancers; Therapeutics; AMYLOID PRECURSOR PROTEIN; CELLULAR PRION PROTEIN; WILD-TYPE P53; C-TERMINAL FRAGMENT; UBIQUITIN-PROTEASOME SYSTEM; STRESS-INDUCIBLE PROTEIN-1; MILD COGNITIVE IMPAIRMENT; GAMMA-SECRETASE CLEAVAGE; ALPHA-SYNUCLEIN PROTECTS; ANTI-APOPTOTIC PHENOTYPE;
D O I
10.1016/j.pharmthera.2013.11.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
More than thirty years elapsed since a protein, not yet called p53 at the time, was detected to bind SV40 during viral infection. Thousands of papers later, p53 evolved as the main tumor suppressor involved in growth arrest and apoptosis. A lot has been done but the protein has not yet revealed all its secrets. Particularly important is the observation that in totally distinct pathologies where apoptosis is either exacerbated or impaired, p53 appears to play a central role. This is exemplified for Alzheimer's and Parkinson's diseases that represent the two main causes of age-related neurodegenerative affections, where cell death enhancement appears as one of the main etiological paradigms. Conversely, in cancers, about half of the cases are linked to mutations in p53 leading to the impairment of p53-dependent apoptosis. The involvement of p53 in these pathologies has driven a huge amount of studies aimed at designing chemical tools or biological approaches to rescue p53 defects or over-activity. Here, we describe the data linking p53 to neurodegenerative diseases and brain cancers, and we document the various strategies to interfere with p53 dysfunctions in these disorders. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:99 / 113
页数:15
相关论文
共 366 条
  • [1] Mammalian prion biology: One century of evolving concepts
    Aguzzi, A
    Polymenidou, M
    [J]. CELL, 2004, 116 (02) : 313 - 327
  • [2] Protective effect of TAT-delivered α-synuclein:: relevance of the C-terminal domain and involvement of HSP70
    Albani, D
    Peverelli, E
    Rametta, R
    Batelli, S
    Veschini, L
    Negro, A
    Forloni, G
    [J]. FASEB JOURNAL, 2004, 18 (12) : 1713 - +
  • [3] Targeting the ubiquitin-proteasome system to activate wild-type p53 for cancer therapy
    Allende-Vega, Nerea
    Saville, Mark K.
    [J]. SEMINARS IN CANCER BIOLOGY, 2010, 20 (01) : 29 - 39
  • [4] Lack of a-disintegrin-and-metalloproteinase ADAM10 leads to intracellular accumulation and loss of shedding of the cellular prion protein in vivo
    Altmeppen, Hermann C.
    Prox, Johannes
    Puig, Berta
    Kluth, Mark A.
    Bernreuther, Christian
    Thurm, Dana
    Jorissen, Ellen
    Petrowitz, Bettina
    Bartsch, Udo
    De Strooper, Bart
    Saftig, Paul
    Glatzel, Markus
    [J]. MOLECULAR NEURODEGENERATION, 2011, 6
  • [5] Interplay Between 20S Proteasomes and Prion Proteins in Scrapie Disease
    Amici, Manila
    Cecarini, Valentina
    Cuccioloni, Massimiliano
    Angeletti, Mauro
    Barocci, Simone
    Rossi, Giacomo
    Fioretti, Evandro
    Keller, Jeffrey N.
    Eleuteri, Anna Maria
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2010, 88 (01) : 191 - 201
  • [6] Opposing roles of prion protein in oxidative stress- and ER stress-induced apoptotic signaling
    Anantharam, Vellareddy
    Kanthasamy, Arthi
    Choi, Christopher J.
    Martin, Dustin P.
    Latchoumycandane, Calivarathan
    Richt, Jueergen A.
    Kanthasamy, Anumantha G.
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2008, 45 (11) : 1530 - 1541
  • [7] Morphological and biochemical assessment of DNA damage and apoptosis in Down syndrome and Alzheimer disease, and effect of postmortem tissue archival on TUNEL
    Anderson, AJ
    Stoltzner, S
    Lai, F
    Su, J
    Nixon, RA
    [J]. NEUROBIOLOGY OF AGING, 2000, 21 (04) : 511 - 524
  • [8] DNA damage and apoptosis in Alzheimer's disease: Colocalization with c-Jun immunoreactivity, relationship to brain area, and effect of postmortem delay
    Anderson, AJ
    Su, JH
    Cotman, CW
    [J]. JOURNAL OF NEUROSCIENCE, 1996, 16 (05) : 1710 - 1719
  • [9] [Anonymous], COLD SPRING HARB PER
  • [10] Endogenous β-amyloid production in presenilin-deficient embryonic mouse fibroblasts
    Armogida, M
    Petit, A
    Vincent, B
    Scarzello, S
    da Costa, CA
    Checler, F
    [J]. NATURE CELL BIOLOGY, 2001, 3 (11) : 1030 - 1033