p63: Defining roles in morphogenesis, homeostasis, and neoplasia of the epidermis

被引:44
作者
King, Kathryn E. [1 ]
Weinberg, Wendy C. [1 ]
机构
[1] FDA Ctr Drug Evaluat & Res, Div Monoclonal Antibodies, Immunobiol Lab, Bethesda, MD 20892 USA
关键词
p63; epidermis; keratinocyte growth regulation; p53; homologues; squamous neoplasia;
D O I
10.1002/mc.20337
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p63 is a member of a gene family also including the p53 tumor suppressor and p73. In contrast to p53, p63 is rarely mutated in human cancers. Rather, gene amplification and dysregulated expression of p63 protein have been observed, particularly in squamous cell carcinomas. p63 is essential for development of stratified squamous epithelium, including the epidermis. The p63 gene is expressed as multiple protein isoforms with different functional capacities, and the balance of these isoforms, along with the presence or absence of the other family members, p53 and p73, can impact biological outcome. Both gene silencing and overexpression approaches have been utilized to elucidate the contributions of specific p63 isoforms to normal epidermal morphogenesis and tissue maintenance. While numerous studies have established the essential nature of p63 in the epidermis, the basis of this requirement, and the unique, as well as, overlapping functions of the individual isoforms, remain controversial. In this review, we summarize the current understanding of roles played by specific p63 isoforms within the context of epidermal morphogenesis and homeostasis of the established epidermis, and the potential impact of p63 dysregulation on cancer development. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:716 / 724
页数:9
相关论文
共 76 条
[11]   Tumor-specific p73 up-regulation mediates p63 dependence in squamous cell carcinoma [J].
DeYoung, Maurice Phillip ;
Johannessen, Cory M. ;
Leong, Chee-Onn ;
Faquin, William ;
Rocco, James W. ;
Ellisen, Leif W. .
CANCER RESEARCH, 2006, 66 (19) :9362-9368
[12]  
Di Como CJ, 2002, CLIN CANCER RES, V8, P494
[13]   p63α and ΔNp63α can induce cell cycle arrest and apoptosis and differentially regulate p53 target genes [J].
Dohn, M ;
Zhang, SZ ;
Chen, XB .
ONCOGENE, 2001, 20 (25) :3193-3205
[14]   p63 and p73 are required for p53-dependent apoptosis in response to DNA damage [J].
Flores, ER ;
Tsai, KY ;
Crowley, D ;
Sengupta, S ;
Yang, A ;
McKeon, F ;
Jacks, T .
NATURE, 2002, 416 (6880) :560-564
[15]   Tumor predisposition in mice mutant for p63 and p73:: Evidence for broader tumor suppressor functions for the p53 family [J].
Flores, ER ;
Sengupta, S ;
Miller, JB ;
Newman, JJ ;
Bronson, R ;
Crowley, D ;
Yang, A ;
McKeon, F ;
Jacks, T .
CANCER CELL, 2005, 7 (04) :363-373
[16]   RACK1 and stratifin target ΔNp63α for a proteasome degradation in head and neck squamous cell carcinoma cells upon DNA damage [J].
Fomenkov, A ;
Zangen, R ;
Huang, YP ;
Osada, M ;
Guo, ZM ;
Fomenkov, T ;
Trink, B ;
Sidransky, D ;
Ratovitski, EA .
CELL CYCLE, 2004, 3 (10) :1285-1295
[17]   δEF1 repressor controls selectively p53 family members during differentiation [J].
Fontemaggi, G ;
Gurtner, A ;
Damalas, A ;
Costanzo, A ;
Higashi, Y ;
Sacchi, A ;
Strano, S ;
Piaggio, G ;
Blandino, G .
ONCOGENE, 2005, 24 (49) :7273-7280
[18]   Complex transcriptional effects of p63 isoforms: Identification of novel activation and repression domains [J].
Ghioni, P ;
Bolognese, F ;
Duijf, PHG ;
van Bokhoven, H ;
Mantovani, R ;
Guerrini, L .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (24) :8659-8668
[19]  
Hagiwara K, 1999, CANCER RES, V59, P4165
[20]   ALTERNATIVELY SPLICED P53-RNA IN TRANSFORMED AND NORMAL-CELLS OF DIFFERENT TISSUE TYPES [J].
HAN, KA ;
KULESZMARTIN, MF .
NUCLEIC ACIDS RESEARCH, 1992, 20 (08) :1979-1981