Medullary thyroid carcinoma: Australian experience with genetic testing.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
J L Ward, V J Hyland, D S Andrew, D J Marsh, B G Robinson
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引用次数: 0

Abstract

Linkage analysis has been performed in four pedigrees with multiple endocrine neoplasia type 2A (MEN 2A) or familial medullary thyroid carcinoma (MTC) using pericentromeric chromosome 10 probes. Important information regarding carrier status has been provided in 10 individuals, many of whom would not have been identified by pentagastrin stimulation testing. We have also used pulsed field gel electrophoresis (PFGE) to link the probes H4.IRBP and pMCK2 to a 150 kb fragment. Using PFGE, no evidence was found in DNA from lymphocytes of a major DNA rearrangement in two individuals affected with MEN 2A and an individual with MEN 2B compared with normals. Metastatic MTC from one patient has been used to generate a cDNA library which will be used to screen for candidate MEN 2A and MEN 2B gene(s).

甲状腺髓样癌:澳大利亚基因检测的经验。
采用10号染色体周粒探针对4例多发性内分泌肿瘤2A型(MEN 2A)或家族性甲状腺髓样癌(MTC)家系进行连锁分析。在10个人中提供了关于携带者状态的重要信息,其中许多人无法通过五宫泌素刺激试验确定。我们还使用脉冲场凝胶电泳(PFGE)连接探针H4。IRBP和pMCK2到150kb片段。使用PFGE,与正常人相比,在两名MEN 2A患者和一名MEN 2B患者的淋巴细胞DNA中未发现重大DNA重排的证据。一名患者的转移性MTC已被用于生成cDNA文库,该文库将用于筛选候选MEN 2A和MEN 2B基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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