Tumour-suppressor function in the nervous system

被引:19
作者
Baker, SJ
McKinnon, PJ
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Genet & Tumour Cell Biol, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrc1297
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumour suppressors prevent cancer by regulating processes such as cell proliferation and survival. However, their functions are diverse, and are often related to the cell type and tissue context. Mutations of tumour-suppressor genes result in unique outcomes in the nervous system that contrast with their roles in other organs. This is closely related to the cell types in which mutations occur and the developmental stage of the tissues that are affected. How can studying the tissue-specific functions of tumour suppressors in the nervous system help us to understand signalling pathways that are relevant to cancer and what are the therapeutic implications of this?.
引用
收藏
页码:184 / 196
页数:13
相关论文
共 140 条
  • [71] The retinoblastoma gene family in differentiation and development
    Lipinski, MM
    Jacks, T
    [J]. ONCOGENE, 1999, 18 (55) : 7873 - 7882
  • [72] Cell-autonomous and non-cell-autonomous functions of the Rb tumor suppressor in developing central nervous system
    Lipinski, MM
    Macleod, KF
    Williams, BO
    Mullaney, TL
    Crowley, D
    Jacks, T
    [J]. EMBO JOURNAL, 2001, 20 (13) : 3402 - 3413
  • [73] Conditional mutation of Rb causes cell cycle defects without apoptosis in the central nervous system
    MacPherson, D
    Sage, J
    Crowley, D
    Trumpp, A
    Bronson, RT
    Jacks, T
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (03) : 1044 - 1053
  • [74] The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate
    Maehama, T
    Dixon, JE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) : 13375 - 13378
  • [75] Rheb fills a GAP between TSC and TOR
    Manning, BD
    Cantley, LC
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2003, 28 (11) : 573 - 576
  • [76] Marino S, 2000, GENE DEV, V14, P994
  • [77] Rb and p107 are required for normal cerebellar development and granule cell survival but not for Purkinje cell persistence
    Marino, S
    Hoogervoorst, D
    Brandner, S
    Berns, A
    [J]. DEVELOPMENT, 2003, 130 (15): : 3359 - 3368
  • [78] Marino S, 2002, DEVELOPMENT, V129, P3513
  • [79] Raf and akt mediate distinct aspects of sensory axon growth
    Markus, A
    Zhong, J
    Snider, WD
    [J]. NEURON, 2002, 35 (01) : 65 - 76
  • [80] PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
    Marsh, DJ
    Kum, JB
    Lunetta, KL
    Bennett, MJ
    Gorlin, RJ
    Ahmed, SF
    Bodurtha, J
    Crowe, C
    Curtis, MA
    Dasouki, M
    Dunn, T
    Feit, H
    Geraghty, MT
    Graham, JM
    Hodgson, SV
    Hunter, A
    Korf, BR
    Manchester, D
    Miesfeldt, S
    Murday, VA
    Nathanson, KL
    Parisi, M
    Pober, B
    Romano, C
    Tolmie, JL
    Trembath, R
    Winter, RM
    Zackai, EH
    Zori, RT
    Weng, LP
    Dahia, PLM
    Eng, C
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (08) : 1461 - 1472