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多重肿瘤抑制基因1纯合缺失在人类星形细胞瘤进展中的作用

Homozygous deletions of the multiple tumor suppressor gene 1 in the progression of human astrocytomas.

作者信息

Walker D G, Duan W, Popovic E A, Kaye A H, Tomlinson F H, Lavin M

机构信息

Department of Surgery, University of Queensland, Herston, Brisbane, Australia.

出版信息

Cancer Res. 1995 Jan 1;55(1):20-3.

PMID:7805033
Abstract

The multiple tumor suppressor gene 1 (MTS1) located on chromosome 9p has recently been implicated as a candidate tumor suppressor gene in many different tumor types. Cytogenetic analysis and deletion mapping studies have revealed that deletion of chromosome 9p occurs in a significant number of primary human astrocytomas. Using multiplex PCR with primers for exon 2 of MTS1 and for D9S196 from chromosome 9q, we have analyzed 78 primary astrocytic tumors for the deletion of MTS1. After controlling for the contamination of tumor samples with normal cells, homozygous loss of MTS1 was found in 13 of 25 anaplastic astrocytomas (WHO grade III) and in 27 of 46 cases of glioblastomas (WHO grade IV) but in none of seven astrocytomas (WHO grade II). These data suggest that MTS1 is an important tumor suppressor gene in the malignant progression of astrocytomas.

摘要

位于9号染色体短臂上的多肿瘤抑制基因1(MTS1)最近被认为是多种不同肿瘤类型中的候选肿瘤抑制基因。细胞遗传学分析和缺失定位研究表明,相当数量的原发性人类星形细胞瘤存在9号染色体短臂缺失。我们使用针对MTS1外显子2和9号染色体长臂上的D9S196的引物进行多重PCR,分析了78例原发性星形细胞肿瘤中MTS1的缺失情况。在控制肿瘤样本被正常细胞污染后,在25例间变性星形细胞瘤(WHO三级)中有13例以及46例胶质母细胞瘤(WHO四级)中有27例发现MTS1纯合缺失,但在7例星形细胞瘤(WHO二级)中均未发现。这些数据表明,MTS1是星形细胞瘤恶性进展中的一个重要肿瘤抑制基因。

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