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巨细胞:与块茎形成的双击模型相悖?

Giant cells: contradiction to two-hit model of tuber formation?

作者信息

Jozwiak Jaroslaw, Jozwiak Sergiusz

机构信息

Department of Histology and Embryology, Center for Biostructure Research, Medical University of Warsaw, and Department of Pediatric Neurology, Children's Memorial Hospital, Warsaw, Poland.

出版信息

Cell Mol Neurobiol. 2005 Aug;25(5):795-805. doi: 10.1007/s10571-005-4932-z.

Abstract
  1. Tuberous sclerosis (TSC) is an autosomal dominant disease characterized by the formation of hamartomatous lesions in many organs, including brain, heart or kidneys. It has been found that TSC is caused by the mutation in one of two tumor suppressor genes: TSC1 or TSC2, encoding hamartin and tuberin, respectively. 2. According to Knudson's two-hit model of tumorigenesis, second-hit mutation and resulting loss of heterozygosity (LOH) of a tumor suppressor gene is necessary for tumor formation. In fact, LOH is commonly found in several types of hamartomas formed in the process of tuberous sclerosis, but, interestingly, not in brain lesions, containing characteristic giant cells. 3. In the present paper we review literature covering origination of giant cells and present several hypotheses explaining why in spite of the presence of hamartin and tuberin, brain lesions form in TSC patients.
摘要
  1. 结节性硬化症(TSC)是一种常染色体显性疾病,其特征是在包括脑、心脏或肾脏在内的许多器官中形成错构瘤性病变。已发现TSC是由两个肿瘤抑制基因之一的突变引起的:TSC1或TSC2,分别编码错构瘤蛋白和结节蛋白。2. 根据Knudson的肿瘤发生双击模型,肿瘤抑制基因的二次打击突变及由此导致的杂合性缺失(LOH)是肿瘤形成所必需的。事实上,在结节性硬化症过程中形成的几种错构瘤类型中普遍发现了LOH,但有趣的是,在含有特征性巨细胞的脑病变中却未发现。3. 在本文中,我们回顾了有关巨细胞起源的文献,并提出了几种假说,以解释为什么尽管存在错构瘤蛋白和结节蛋白,TSC患者仍会形成脑病变。

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