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骨肉瘤和软组织肉瘤中p53基因的突变谱

Mutation spectrum of the p53 gene in bone and soft tissue sarcomas.

作者信息

Toguchida J, Yamaguchi T, Ritchie B, Beauchamp R L, Dayton S H, Herrera G E, Yamamuro T, Kotoura Y, Sasaki M S, Little J B

机构信息

Howe Laboratory of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston 02114.

出版信息

Cancer Res. 1992 Nov 15;52(22):6194-9.

PMID:1423262
Abstract

We present here an analysis of the spectrum of mutations of the p53 gene seen in 127 bone and soft tissue sarcomas of various histological classifications. Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire coding sequence (exons 2 through 11) were identified by a combination of single-strand conformation polymorphism analysis and direct genomic sequencing. A total of 42 somatic alterations of the p53 gene were found, of which 21 were gross rearrangements and 21 were subtle alterations. These included 17 cases of a single base substitution, 3 small deletions, and one single base insertion. In contrast to reported findings for other types of cancer, we found that mutations of the p53 gene in sarcomas are quite heterogeneous both in their distribution throughout the gene and in the type of genetic alterations that result. All 13 missense mutations we found occurred at highly conserved residues, whereas 8 nonsense mutations occurred at sites that spanned the gene from codons 46 to 316. Surprisingly, approximately one-half of the osteosarcomas with allelic deletions on 17p did not have detectable alterations in the coding sequence of the p53 gene.

摘要

我们在此展示了对127例不同组织学分类的骨与软组织肉瘤中p53基因突变谱的分析。通过使用来自p53基因的互补DNA探针进行Southern印迹分析来检测大片段重排,并通过单链构象多态性分析和直接基因组测序相结合的方法来鉴定整个编码序列(外显子2至11)中的细微改变。共发现42例p53基因的体细胞改变,其中21例为大片段重排,21例为细微改变。这些改变包括17例单碱基替换、3例小缺失和1例单碱基插入。与其他类型癌症的报道结果相反,我们发现肉瘤中p53基因的突变在整个基因中的分布以及所导致的基因改变类型方面都具有相当大的异质性。我们发现的所有13个错义突变均发生在高度保守的残基上,而8个无义突变则发生在从密码子46到316跨越该基因的位点上。令人惊讶的是,约一半在17p上存在等位基因缺失的骨肉瘤在p53基因的编码序列中未检测到改变。

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