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在一个大型波利尼西亚家族中,年轻患者发生的侵袭性垂体腺瘤,该家族的AIP基因存在种系R271W突变。

Aggressive pituitary adenomas occurring in young patients in a large Polynesian kindred with a germline R271W mutation in the AIP gene.

作者信息

Jennings Juliet E, Georgitsi Marianthi, Holdaway Ian, Daly Adrian F, Tichomirowa Maria, Beckers Albert, Aaltonen Lauri A, Karhu Auli, Cameron Fergus J

机构信息

Department of Endocrinology and Diabetes and Centre for Hormone Research, The Murdoch Childrens Research Institute and The Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Victoria 3052, Australia.

出版信息

Eur J Endocrinol. 2009 Nov;161(5):799-804. doi: 10.1530/EJE-09-0406. Epub 2009 Aug 14.

Abstract

OBJECTIVE

Mutations in the aryl hydrocarbon receptor-interacting protein (AIP) were recently shown to confer a pituitary adenoma predisposition in patients with familial isolated pituitary adenomas (FIPA). We report a large Samoan FIPA kindred from Australia/New Zealand with an R271W mutation that was associated with aggressive pituitary tumors.

DESIGN AND METHODS

Case series with germline screening of AIP and haplotype analyses among R271W families.

RESULTS

This previously unreported kindred consisted of three affected individuals that either presented with or had first symptoms of a pituitary macroadenoma in late childhood or adolescence. The index case, a 15-year-old male with incipient gigantism and his maternal aunt, had somatotropinomas, and the maternal uncle of the index case had a prolactinoma. All tumors were large (15, 40, and 60 mm maximum diameter) and two required transcranial surgery and radiotherapy. All three affected subjects and ten other unaffected relatives were found to be positive for a germline R271W AIP mutation. Comparison of the single nucleotide polymorphism patterns among this family and two previously reported European FIPA families with the same R271W mutation demonstrated no common ancestry.

CONCLUSIONS

This kindred exemplifies the aggressive features of pituitary adenomas associated with AIP mutations, while genetic analyses among three R271W FIPA families indicate that R271W represents a mutational hotspot that should be studied further in functional studies.

摘要

目的

最近研究表明,芳烃受体相互作用蛋白(AIP)突变会使家族性孤立性垂体腺瘤(FIPA)患者易患垂体腺瘤。我们报告了一个来自澳大利亚/新西兰的大型萨摩亚FIPA家族,该家族携带R271W突变,与侵袭性垂体肿瘤相关。

设计与方法

对AIP进行种系筛查的病例系列研究以及对R271W家族进行单倍型分析。

结果

这个之前未报告的家族中有三名受影响个体,他们在儿童晚期或青春期出现垂体大腺瘤或有垂体大腺瘤的首发症状。索引病例是一名15岁患有早期巨人症的男性,他和他的舅妈患有生长激素瘤,索引病例的舅舅患有催乳素瘤。所有肿瘤都很大(最大直径分别为15、40和60毫米),其中两例需要进行开颅手术和放疗。所有三名受影响的受试者以及其他十名未受影响的亲属均被发现携带种系R271W AIP突变。将该家族与另外两个先前报道的具有相同R271W突变的欧洲FIPA家族的单核苷酸多态性模式进行比较,结果表明它们没有共同的祖先。

结论

这个家族体现了与AIP突变相关的垂体腺瘤的侵袭性特征,而对三个R271W FIPA家族的基因分析表明,R271W代表一个突变热点,应在功能研究中进一步研究。

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