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原发性非小细胞肺癌中p15和p16基因的共缺失

Codeletion of p15 and p16 genes in primary non-small cell lung carcinoma.

作者信息

Xiao S, Li D, Corson J M, Vijg J, Fletcher J A

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Cancer Res. 1995 Jul 15;55(14):2968-71.

PMID:7606711
Abstract

Chromosome band 9p21 is deleted frequently in non-small cell lung carcinoma (NSCLC), and the p15 and p16 cyclin-dependent kinase-4 inhibitor genes map within this deletion region. Recent studies demonstrated deletion of p15 and p16 in NSCLC metastases and cell lines, suggesting a role for these genes in NSCLC progression. We now report p15 and p16 copy number, as determined by fluorescence in situ hybridization with a P1 contig, in 18 primary NSCLCs. Codeletion of p15 and p16 was found in 15 of 18 NSCLCs, and 1 of the 3 tumors with normal p15 and p16 copy number had a nonsense mutation in exon 2 of p16. We conclude that p15 and p16 are deleted and/or mutated in most primary NSCLCs. Two observations, however, support the involvement of at least one additional tumor suppressor gene on chromosome 9. These observations are: (a) the large size (> 100 kb) of most NSCLC p15/p16 deletions; and (b) the absence of exon 2 mutations in most retained NSCLC p15 and p16 alleles.

摘要

在非小细胞肺癌(NSCLC)中,9号染色体21区带(9p21)经常发生缺失,而p15和p16细胞周期蛋白依赖性激酶4抑制基因定位于此缺失区域内。最近的研究表明,在NSCLC转移灶和细胞系中存在p15和p16的缺失,提示这些基因在NSCLC进展中发挥作用。我们现在报告通过使用P1重叠群荧光原位杂交确定的18例原发性NSCLC中p15和p16的拷贝数。在18例NSCLC中有15例发现p15和p16共缺失,在3例p15和p16拷贝数正常的肿瘤中有1例在p16外显子2存在无义突变。我们得出结论,在大多数原发性NSCLC中p15和p16发生缺失和/或突变。然而,有两个观察结果支持9号染色体上至少还有一个额外的肿瘤抑制基因参与其中。这些观察结果为:(a)大多数NSCLC中p15/p16缺失的大片段(>100 kb);(b)大多数保留的NSCLC p15和p16等位基因中无外显子2突变。

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