Roles of the Nkx3.1 homeobox gene in prostate organogenesis and carcinogenesis

被引:79
作者
Shen, MM
Abate-Shen, C
机构
[1] UMDNJ Robert Wood Johnson Med Sch, Inst Canc, Ctr Adv Biotechnol & Med, Piscataway, NJ USA
[2] UMDNJ Robert Wood Johnson Med Sch, Inst Canc, Dept Pediat, Piscataway, NJ USA
[3] UMDNJ Robert Wood Johnson Med Sch, Inst Canc, Dept Med, Piscataway, NJ USA
[4] UMDNJ Robert Wood Johnson Med Sch, Inst Canc, Dept Neurosci & Cell Biol, Piscataway, NJ USA
关键词
urogenital development; transcription factor; epithelial-mesenchymal interaction; tumor suppressor; haploinsufficiency; mouse models for cancer;
D O I
10.1002/dvdy.10397
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Although it is often presumed that the molecular pathways that underlie normal organogenesis are similar to those perturbed during carcinogenesis, few examples exist of tissue-specific regulatory genes that play central roles in both processes. In the case of the prostate gland, molecular genetic analyses have demonstrated that the Nkx3.1 homeobox gene plays an important role in normal differentiation of the prostatic epithelium and that its loss of function is an initiating event in prostate carcinogenesis. Thus, the Nkx3.1 homeobox gene provides a paradigm for understanding the relationship between normal differentiation and cancer, as well as a model for studying the roles of homeobox genes in these processes. Here, we review recent findings concerning the biological as well as biochemical function of this central regulator of prostate development and carcinogenesis. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:767 / 778
页数:12
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