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一名颅内室管膜瘤患者p53基因种系突变的鉴定。

Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma.

作者信息

Metzger A K, Sheffield V C, Duyk G, Daneshvar L, Edwards M S, Cogen P H

机构信息

Brain Tumor Research Center, University of California, San Francisco 94143.

出版信息

Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7825-9. doi: 10.1073/pnas.88.17.7825.

Abstract

We detected a germ-line mutation of the p53 gene in a patient with a malignant ependymoma of the posterior fossa. This mutation, which was found at codon 242, resulted in an amino acid substitution in a highly conserved site of exon 7 of the p53 gene; the same mutation was found in both the germ-line and the tumor tissue. This is the most common region of previously described somatic p53 mutations in tumor specimens and of the germ-line p53 mutations in patients with the Li-Fraumeni cancer syndrome. Evaluation of the patient's family revealed several direct maternal and paternal relatives who had died at a young age from different types of cancer. The association of a germ-line p53 mutation with an intracranial malignancy and a strong family history of cancer suggests that p53 gene mutations predispose a person to malignancy and, like retinoblastoma mutations, may be inherited.

摘要

我们在一名患有后颅窝恶性室管膜瘤的患者中检测到p53基因的种系突变。该突变位于密码子242,导致p53基因第7外显子高度保守位点的氨基酸替换;在种系和肿瘤组织中均发现了相同的突变。这是先前在肿瘤标本中描述的体细胞p53突变以及李-佛美尼癌症综合征患者种系p53突变最常见的区域。对患者家族的评估发现,有几位直系母系和父系亲属在年轻时死于不同类型的癌症。种系p53突变与颅内恶性肿瘤以及强烈的癌症家族史之间的关联表明,p53基因突变使个体易患恶性肿瘤,并且与视网膜母细胞瘤突变一样,可能是可遗传的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c32/52396/adcec0432d87/pnas01067-0378-a.jpg

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