P53, apoptosis and axon-guidance molecules

被引:66
作者
Arakawa, H [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Canc Med & Biophys Div, Chuo Ku, Tokyo 1040045, Japan
关键词
p53; tumor suppressor; cancer; apoptosis; UNC5B; netrin-1;
D O I
10.1038/sj.cdd.4401601
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
The p53 tumor-suppressor gene regulates apoptosis through the transcriptional activation of its target genes. The expression of the axon-guidance molecule UNC5B (also designated p53RDL1), which is a receptor for netrin-1, is directly regulated by p53. In the absence of netrin-1, UNC5B mediates p53-dependent apoptosis. Conversely, in the presence of netrin-1, p53-induced apoptosis is inhibited through the signaling pathway activated by the interaction between netrin-1 and UNC5B. A number of other molecules that are involved in axon guidance are inactivated in human cancers and are also regulated by p53. These findings suggest a close link between axon-guidance molecules and tumorigenesis.
引用
收藏
页码:1057 / 1065
页数:9
相关论文
共 90 条
[41]   Slit-Robo: Neuronal guides signal in tumor angiogenesis [J].
Liu, ZJ ;
Herlyn, M .
CANCER CELL, 2003, 4 (01) :1-2
[42]   Netrin-1 acts as a survival factor via its receptors UNC5H and DCC [J].
Llambi, F ;
Causeret, F ;
Bloch-Gallego, E ;
Mehlen, P .
EMBO JOURNAL, 2001, 20 (11) :2715-2722
[43]   Netrin-1 controls colorectal tumorigenesis by regulating apoptosis [J].
Mazelin, L ;
Bernet, A ;
Bonod-Bidaud, C ;
Pays, L ;
Arnaud, S ;
Gespach, C ;
Bredesen, DE ;
Scoazec, JY ;
Mehlen, P .
NATURE, 2004, 431 (7004) :80-84
[44]   The dependence receptor hypothesis [J].
Mehlen, P ;
Bredesen, DE .
APOPTOSIS, 2004, 9 (01) :37-49
[45]   The DCC gene product induces apoptosis by a mechanism requiring receptor proteolysis [J].
Mehlen, P ;
Rabizadeh, S ;
Snipas, SJ ;
Assa-Munt, N ;
Salvesen, GS ;
Bredesen, DE .
NATURE, 1998, 395 (6704) :801-804
[46]  
MEHLEN P, 2003, SCI STKE, pPE55
[47]  
Meyerhardt JA, 1999, CELL GROWTH DIFFER, V10, P35
[48]   Identification of a chromosome 3p14.3-21.1 gene, APPL, encoding an adaptor molecule that interacts with the oncoprotein-serine/threonine kinase AKT2 [J].
Mitsuuchi, Y ;
Johnson, SW ;
Sonoda, G ;
Tanno, S ;
Golemis, EA ;
Testa, JR .
ONCOGENE, 1999, 18 (35) :4891-4898
[49]  
MIYASHITA T, 1995, CELL, V80, P293
[50]   Apaf-1 is a transcriptional target for E2F and p53 [J].
Moroni, MC ;
Hickman, ES ;
Denchi, EL ;
Caprara, G ;
Colli, E ;
Cecconi, F ;
Müller, H ;
Helin, K .
NATURE CELL BIOLOGY, 2001, 3 (06) :552-558