Notch signalling in T-cell lymphoblastic leukaemia/lymphoma and other haematological malignancies

被引:134
作者
Aster, Jon C. [1 ]
Blacklow, Stephen C. [2 ,3 ]
Pear, Warren S. [4 ]
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Dept Pathol, Sch Med, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
关键词
Notch signalling; oncogene; T-cell lymphoblastic leukaemia/lymphoma; chromosomal rearrangements; targeted therapy; NF-KAPPA-B; C-MYC; GENE-EXPRESSION; TRANSCRIPTIONAL ACTIVATION; PROGNOSTIC-SIGNIFICANCE; REGULATORY REGION; PROMOTES SURVIVAL; ALAGILLE-SYNDROME; TUMOR-SUPPRESSOR; STRUCTURAL BASIS;
D O I
10.1002/path.2789
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Notch receptors participate in a highly conserved signalling pathway that regulates normal development and tissue homeostasis in a context-and dose-dependent manner. Deregulated Notch signalling has been implicated in many diseases, but the clearest example of a pathogenic role is found in T-cell lymphoblastic leukaemia/lymphoma (T-LL), in which the majority of human and murine tumours have acquired mutations that lead to aberrant increases in Notch1 signalling. Remarkably, it appears that the selective pressure for Notch mutations is virtually unique among cancers to T-LL, presumably reflecting a special context-dependent role for Notch in normal T-cell progenitors. Nevertheless, there are some recent reports suggesting that Notch signalling has subtle, yet important roles in other forms of haematological malignancy as well. Here, we review the role of Notch signalling in various blood cancers, focusing on T-LL with an eye towards targeted therapeutics. Copyright (C) 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:262 / 273
页数:12
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