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生长激素瘤与11号染色体上等位基因缺失及gsp突变的关联。

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.

作者信息

Thakker R V, Pook M A, Wooding C, Boscaro M, Scanarini M, Clayton R N

机构信息

M.R.C. Molecular Medicine Group, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.

出版信息

J Clin Invest. 1993 Jun;91(6):2815-21. doi: 10.1172/JCI116524.

Abstract

The molecular pathology of somatotrophinomas has been investigated by a combined search for dominant mutations of the gene encoding the Gs alpha protein and for recessive mutations involving chromosome 11q13, which contains the gene causing multiple endocrine neoplasia type 1 (MEN1). Somatotrophinomas and peripheral leukocytes were obtained from thirteen patients with acromegaly; one patient also suffered from MEN1. Five DNA probes identifying restriction fragment length polymorphisms from 11q revealed allele loss in pituitary tumors from five (four non-MEN1 and one MEN1) patients. Deletion mapping revealed that the region of allele loss common to the somatotrophinomas involved 11q13. An analysis for similar allelic deletions at 12 other loci from chromosomes 1-5, 7-9, 12-14, and 17 did not reveal generalized allele loss in the somatotrophinomas. These results, which represent the first report of chromosome 11 allele loss occurring in non-MEN1 somatotrophinomas, indicate that a recessive oncogene on 11q13 is specifically involved in the monoclonal development of somatotrophinomas. In addition Gs alpha mutations were detected in two non-MEN1 somatotrophinomas, one of which also revealed allele loss of chromosome 11. Thus, our results reveal that the development of somatotrophinomas is associated with alterations in both dominant and recessive oncogenes and further characterization of these genetic abnormalities will help to elucidate the multistep etiology and progression of somatotrophinomas.

摘要

通过联合搜索编码Gsα蛋白的基因的显性突变以及涉及11q13染色体的隐性突变(该染色体包含导致1型多发性内分泌腺瘤病(MEN1)的基因),对生长激素瘤的分子病理学进行了研究。从13例肢端肥大症患者中获取了生长激素瘤和外周血白细胞;其中1例患者还患有MEN1。5个识别11q限制性片段长度多态性的DNA探针显示,5例患者(4例非MEN1患者和1例MEN1患者)的垂体肿瘤存在等位基因缺失。缺失图谱显示,生长激素瘤共有的等位基因缺失区域涉及11q13。对来自1 - 5号、7 - 9号、12 - 14号和17号染色体的其他12个位点的类似等位基因缺失进行分析,未发现生长激素瘤存在普遍的等位基因缺失。这些结果是关于非MEN1生长激素瘤中发生11号染色体等位基因缺失的首次报道,表明11q13上的一个隐性癌基因特别参与了生长激素瘤的单克隆发展。此外,在2例非MEN1生长激素瘤中检测到Gsα突变,其中1例还显示11号染色体等位基因缺失。因此,我们的结果表明,生长激素瘤的发生与显性和隐性癌基因的改变有关,对这些基因异常的进一步表征将有助于阐明生长激素瘤的多步骤病因和进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da0/443349/97d645e58832/jcinvest00055-0487-a.jpg

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