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混合性髓样-滤泡性甲状腺癌。肿瘤成分双重起源的分子证据。

Mixed medullary-follicular thyroid carcinoma. Molecular evidence for a dual origin of tumor components.

作者信息

Volante M, Papotti M, Roth J, Saremaslani P, Speel E J, Lloyd R V, Carney J A, Heitz P U, Bussolati G, Komminoth P

机构信息

Department of Biomedical Sciences, University of Turin, Turin, Italy.

出版信息

Am J Pathol. 1999 Nov;155(5):1499-509. doi: 10.1016/S0002-9440(10)65465-X.

Abstract

Mixed medullary-follicular carcinomas (MMFCs) are tumors of the thyroid that display morphological and immunohistochemical features of both medullary and follicular neoplasms. The histogenetic origin and possible molecular mechanisms leading to MMFCs are still unclear. To address these questions, we have isolated the two histological components of 12 MMFCs by (laser-based) microdissection, analyzed them for mutations in the RET proto-oncogene and allelic losses of nine loci on six chromosomes, and studied the clonal composition of MMFCs in female patients. Our results provide strong evidence that the follicular and medullary components in MMFCs are not derived from a single progenitor cell, because the seven tumors amenable for analysis consistently exhibited a different pattern of mutations, allelic losses, and clonal composition. We also demonstrate that follicular structures in MMFCs are often oligo/polyclonal and more frequently exhibit hyperplastic than neoplastic histological features, indicating that at least a subset of MMFCs are composed of a medullary thyroid carcinoma containing hyperplastic follicles.

摘要

混合性髓样-滤泡状癌(MMFCs)是甲状腺肿瘤,具有髓样和滤泡性肿瘤的形态学及免疫组化特征。MMFCs的组织发生起源以及导致其发生的可能分子机制仍不清楚。为解决这些问题,我们通过(基于激光的)显微切割分离了12例MMFCs的两种组织学成分,分析它们RET原癌基因的突变以及六条染色体上九个位点的等位基因缺失情况,并研究了女性患者MMFCs的克隆组成。我们的结果提供了强有力的证据,表明MMFCs中的滤泡性和髓样成分并非源自单个祖细胞,因为七例适合分析的肿瘤一致呈现出不同的突变模式、等位基因缺失情况及克隆组成。我们还证明,MMFCs中的滤泡结构通常为寡克隆/多克隆性,且相较于肿瘤性组织学特征,更常表现出增生性组织学特征,这表明至少一部分MMFCs由含有增生性滤泡的甲状腺髓样癌组成。

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