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原发性恶性间皮瘤中p15和p16的共同缺失

Codeletion of p15 and p16 in primary malignant mesothelioma.

作者信息

Xio S, Li D, Vijg J, Sugarbaker D J, Corson J M, Fletcher J A

机构信息

Department of Pathology, Children's Hospital, Boston, Massachusetts USA.

出版信息

Oncogene. 1995 Aug 3;11(3):511-5.

PMID:7630635
Abstract

The p15 and p16 CDK4 inhibitor genes map within the chromosome band 9p21 region deleted frequently in malignant mesothelioma and other cancers. p16 has been implicated recently as a potential target of 9p21 deletions in mesothelioma, but the role of this gene is uncertain because deletions have been detected more often in established cell lines than in primary tumor specimens. We determined p15 and p16 copy number by fluorescence in situ hybridization with a P1 contig in 50 primary mesotheliomas. Codeletion of p15 and p16 was found in 72% of mesotheliomas, including all cases with spindle-cell components (n = 21) and total deletion of p15 and p16 was found in several mesotheliomas that lacked cytogenetic deletion of the chromosome 9 short arm. Point mutations were not found, however, in exon 2 of retained p15 and p16 alleles from seven mesotheliomas. These findings demonstrate that p15, p16 and/or a closely neighboring gene, are the targets of frequent chromosome 9p deletion in primary malignant mesothelioma.

摘要

p15和p16细胞周期蛋白依赖性激酶4(CDK4)抑制基因定位于9p21染色体带区域,该区域在恶性间皮瘤和其他癌症中经常缺失。最近,p16被认为是间皮瘤中9p21缺失的一个潜在靶点,但由于在已建立的细胞系中比在原发性肿瘤标本中更频繁地检测到缺失,该基因的作用尚不确定。我们通过荧光原位杂交技术,利用P1重叠群对50例原发性间皮瘤中的p15和p16拷贝数进行了测定。在72%的间皮瘤中发现了p15和p16的共同缺失,包括所有具有梭形细胞成分的病例(n = 21),并且在一些缺乏9号染色体短臂细胞遗传学缺失的间皮瘤中发现了p15和p16的完全缺失。然而,在7例间皮瘤保留的p15和p16等位基因的第2外显子中未发现点突变。这些发现表明,p15、p16和/或一个紧密相邻的基因是原发性恶性间皮瘤中9p染色体频繁缺失的靶点。

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