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去分化脂肪肉瘤中p53信号通路的分子异常

Molecular abnormalities of the p53 pathway in dedifferentiated liposarcoma.

作者信息

Dei Tos A P, Doglioni C, Piccinin S, Maestro R, Mentzel T, Barbareschi M, Boiocchi M, Fletcher C D

机构信息

Department of Pathology, Hospital of Treviso, Belluno, Italy.

出版信息

J Pathol. 1997 Jan;181(1):8-13. doi: 10.1002/(SICI)1096-9896(199701)181:1<8::AID-PATH700>3.0.CO;2-#.

Abstract

Dedifferentiated liposarcoma represents a distinct subtype of liposarcoma and is characterized by the presence of abrupt transition from well-differentiated liposarcoma to high-grade pleomorphic sarcoma (mostly MFH-like). A key role for p53 in tumour progression of this subset of liposarcomas has been suggested on the basis of p53 immunopositivity. A series of 14 dedifferentiated liposarcomas has been investigated by analysing the p53 gene and protein together with the p53-related molecules p21Waf1 and mdm2, to verify whether the p53 pathway is involved in the development and progression of this tumour type. The results indicate that the p53 gene is rarely involved in dedifferentiated liposarcoma (7 per cent of cases analysed) and that low percentages of p53 immunopositivity are still compatible with integrity of the p53 gene. This concept is also supported by the observed preservation of p21Waf1 immunoreactivity in all but the p53-mutated cases. By contrast, mdm2 overexpression emerges as the most frequent abnormality in dedifferentiated liposarcoma (57 and 78 per cent of cases in well-differentiated and high-grade areas, respectively).

摘要

去分化脂肪肉瘤是脂肪肉瘤的一种独特亚型,其特征是存在从高分化脂肪肉瘤到高级别多形性肉瘤(大多为黏液纤维肉瘤样)的突然转变。基于p53免疫阳性,有人提出p53在这一亚型脂肪肉瘤的肿瘤进展中起关键作用。通过分析p53基因和蛋白以及与p53相关的分子p21Waf1和mdm2,对一系列14例去分化脂肪肉瘤进行了研究,以验证p53通路是否参与了这种肿瘤类型的发生和发展。结果表明,p53基因很少参与去分化脂肪肉瘤(分析病例的7%),低百分比的p53免疫阳性仍与p53基因的完整性相符。除p53突变病例外,所有病例中p21Waf1免疫反应性的保留也支持了这一概念。相比之下,mdm2过表达是去分化脂肪肉瘤中最常见的异常情况(在高分化和高级别区域分别为57%和78%的病例)。

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