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在一名具有Y衍生标记染色体的特纳综合征嵌合患者的单侧微小性腺母细胞瘤中检测TSPY蛋白。

Detection of TSPY protein in a unilateral microscopic gonadoblastoma of a Turner mosaic patient with a Y-derived marker chromosome.

作者信息

Hildenbrand R, Schröder W, Brude E, Schepler A, König R, Stutte H J, Arnemann J

机构信息

Department of Pathology, University Hospital, Frankfurt/M., Germany.

出版信息

J Pathol. 1999 Dec;189(4):623-6. doi: 10.1002/(SICI)1096-9896(199912)189:4<623::AID-PATH475>3.0.CO;2-#.

Abstract

Gonadoblastomas are seen almost exclusively in dysgenetic gonads of patients with a chromosomal mosaicism of 45,X and an additional Y-bearing cell line. This paper presents a case of a Turner mosaic patient with 45,X/46,X,+mar karyotype, who developed a unilateral microscopic gonadoblastoma. Cytogenetic and molecular analysis confirmed a Y-chromosomal origin of the marker chromosome, with a deletion of the distal Yq arm and the proposed region of a so far undefined gonadoblastoma locus (GBY) present. One of the candidate genes within the postulated GBY region is TSPY (testis-specific protein Y-encoded). To study the TSPY protein expression, an anti-fusion protein antibody was used for immunohistochemistry of the patient's gonads. In contrast to the dysgenetic gonad, an intense immunoreaction was found in gonadoblastoma tumour cells of the other gonad. These results confirm the high level of TSPY protein expression by these cells and demonstrate the value of this antibody as an additional marker to confirm the diagnosis of gonadoblastoma.

摘要

性腺母细胞瘤几乎仅见于染色体嵌合体为45,X并伴有额外含Y细胞系的患者发育异常的性腺中。本文报告了一例核型为45,X/46,X,+mar的特纳嵌合体患者,其单侧发生了微小性腺母细胞瘤。细胞遗传学和分子分析证实标记染色体起源于Y染色体,Yq臂远端缺失,且存在一个迄今未明确的性腺母细胞瘤位点(GBY)的假定区域。假定的GBY区域内的候选基因之一是TSPY(睾丸特异性蛋白Y编码)。为研究TSPY蛋白表达,使用抗融合蛋白抗体对患者性腺进行免疫组织化学检测。与发育异常的性腺不同,在另一个性腺的性腺母细胞瘤肿瘤细胞中发现了强烈的免疫反应。这些结果证实了这些细胞中TSPY蛋白的高表达水平,并证明了该抗体作为确认性腺母细胞瘤诊断的辅助标志物的价值。

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