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通过人雄激素受体(HUMARA)基因检测对良性甲状旁腺病变进行克隆性分析。

Clonality Analysis of Benign Parathyroid Lesions by Human Androgen Receptor (HUMARA) Gene Assay.

作者信息

Sanjuan Xavier, Bryant Bonita R., Sobel Mark E., Merino Maria I.

出版信息

Endocr Pathol. 1998 Winter;9(1):293-300. doi: 10.1007/BF02739689.

Abstract

Benign conditions of the parathyroid gland have been classified as adenomas and hyperplasias. These entities however are difficult to distinguish when only a single gland is enlarged. Adenomas are defined as neoplastic clonal growths whereas hyperplasias are considered to be reactive processes of polyclonal origin. In order to analyze the clonal pattern of these lesions, we have studied hyperplasias and adenomas of parathyroid glands from women by the human androgen receptor (HUMARA) assay, a recently reliable and highly-lnformative technique based on the X-chromosome inactivation pattern in females. Samples consisted of formalin-fixed as well as frozen tissues. Informativeness with HUMARA marker was 87% (13/15 cases). All hyperplasias (5/5) and 6/8 adenomas yielded polyclonal results, since two alleles of similar intensity appeared when the lesion was HpaIl-digested. Two parathyroid adenomas had a loss of one X-alIeIe for the HUMARA gene and they were interpreted as monoclonal. These results show that parathyroid hyperplasias and adenomas, considered as multigland or monogland involvement diseases respectively, may be both polyclonal in origin, and that only a small subset of adenomas is found to be clonal. Consequently, clonality analysis cannot allow a clear distinction between these two entities as classically diagnosed. A different approach should be considering hyperplasia or adenoma when a polyclonal or monoclonal result has been obtained by clonality analysis.

摘要

甲状旁腺的良性病变已被分类为腺瘤和增生。然而,当仅一个腺体增大时,这些实体很难区分。腺瘤被定义为肿瘤性克隆生长,而增生被认为是多克隆起源的反应性过程。为了分析这些病变的克隆模式,我们通过人类雄激素受体(HUMARA)检测研究了女性甲状旁腺的增生和腺瘤,这是一种基于女性X染色体失活模式的近期可靠且信息丰富的技术。样本包括福尔马林固定以及冷冻组织。HUMARA标记的信息性为87%(15例中的13例)。所有增生(5/5)和8例腺瘤中的6例产生多克隆结果,因为当病变经HpaII消化时出现两个强度相似的等位基因。两个甲状旁腺腺瘤的HUMARA基因有一个X等位基因缺失,它们被解释为单克隆。这些结果表明,分别被视为多腺体或单腺体受累疾病的甲状旁腺增生和腺瘤可能都起源于多克隆,并且仅发现一小部分腺瘤是克隆性的。因此,克隆性分析无法像经典诊断那样明确区分这两个实体。当通过克隆性分析获得多克隆或单克隆结果时,应采用不同的方法来考虑增生或腺瘤。

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