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利用微卫星标记对头颈部鳞状细胞癌3号染色体短臂上肿瘤抑制基因位点的定义。

Definition of a tumor suppressor gene locus on the short arm of chromosome 3 in squamous cell carcinoma of the head and neck by means of microsatellite markers.

作者信息

Rowley H, Jones A, Spandidos D, Field J

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of Liverpool, England.

出版信息

Arch Otolaryngol Head Neck Surg. 1996 May;122(5):497-501. doi: 10.1001/archotol.1996.01890170031007.

DOI:10.1001/archotol.1996.01890170031007
PMID:8615966
Abstract

BACKGROUND

Tumor suppressor genes are important in the development of head and neck cancer. Using microsatellite markers that map close to the region 3p24-pter, we determined the frequency of allele loss close to this site with a view to narrowing the search for a putative tumor suppressor gene involved in the development of squamous cell carcinoma of the head and neck, which may facilitate future positional cloning techniques.

DESIGN

Laboratory-based project with tumor and normal specimens subjected to molecular genetic analysis. Tumor-normal tissue DNA pairs were analyzed for allelic imbalance and microsatellite instability on chromosome 3p in the region 3p24-pter by the polymerase chain reaction and microsatellite markers D3S1304, D3S656, D3S1252, D3S1293, THRB, and D3S1266.

SETTING

Molecular genetics and oncology research laboratory.

PATIENTS

Paired tumor-normal DNA samples were obtained from 46 patients with tumors of the head and neck.

MAIN OUTCOME MEASURES

Detection of loss of heterozygosity and microsatellite instability on chromosome 3 in the region 3p24-p25.1.

RESULTS

We found loss of heterozygosity with at least one marker in 48% of informative cases and loss of heterozygosity or microsatellite instability in 57% of informative cases. The minimal region of loss was found in the region bounded by D3S656 and D31293.

CONCLUSION

A putative tumor suppressor gene in head and neck cancer lies between D3S656 and D3S1293 in the 3p25.1 region.

摘要

背景

肿瘤抑制基因在头颈癌的发生发展中起重要作用。利用定位在3p24 - pter区域附近的微卫星标记,我们确定了该位点附近等位基因缺失的频率,以期缩小对头颈鳞状细胞癌发生发展中假定肿瘤抑制基因的搜索范围,这可能有助于未来的定位克隆技术。

设计

基于实验室的项目,对肿瘤和正常标本进行分子遗传学分析。通过聚合酶链反应和微卫星标记D3S1304、D3S656、D3S1252、D3S1293、THRB和D3S1266,分析肿瘤 - 正常组织DNA对在3p24 - pter区域3号染色体上的等位基因不平衡和微卫星不稳定性。

地点

分子遗传学和肿瘤学研究实验室。

患者

从46例头颈肿瘤患者中获取配对的肿瘤 - 正常DNA样本。

主要观察指标

检测3p24 - p25.1区域3号染色体上杂合性缺失和微卫星不稳定性。

结果

我们在48%的信息性病例中发现至少一个标记存在杂合性缺失,在57%的信息性病例中发现杂合性缺失或微卫星不稳定性。缺失的最小区域位于D3S656和D31293之间。

结论

头颈癌中的假定肿瘤抑制基因位于3p25.1区域的D3S656和D3S1293之间。

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