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Molecular genetic evidence supporting the neoplastic nature of fibrous stroma in testicular teratoma

机译:分子遗传学证据支持睾丸畸胎瘤中纤维基质的赘生性

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Testicular teratoma typically consists of heterogeneous mixtures of diverse epithelial and stromal components. The biological nature and genetic characteristics of the fibrous stroma of testicular teratomas have not been thoroughly investigated. Chromosome 12p abnormalities are the hallmark genetic alterations of germ cell tumors. We studied chromosome 12p abnormalities in the fibrous stroma and other components of pure testicular teratomas from 32 patients using interphase fluorescence in situ hybridization. Overall, 72% (23/32) of pure testicular teratomas had chromosome 12p abnormalities. Isochromosome 12p or 12p overrepresentation independent of isochromosome 12p was detected in the fibrous stroma in 53% (17/32) and 41% (13/32) of cases, respectively. Among the 17 cases positive for isochromosome 12p, 8 (47%) also had 12p overrepresentation. In 31% (10/32) cases, the fibrous stroma showed neither 12p overrepresentation nor isochromosome 12p. Isochromosome 12p and 12p overrepresentation were identified, respectively, in the gastrointestinal-type epithelium of 14/23 (61%) and 15/23 (65%) cases; in the respiratory-type epithelium of 41% (7/17) and 41% (7/17) cases; in the squamous epithelium of 62% (8/13) and 54% (7/13) cases; and in the cartilage of 63% (5/8) and 38% (3/8) cases. Concordant chromosomal 12p abnormalities were observed between the fibrous stroma and epithelial elements of testicular teratomas. Our results indicate that the fibrous stroma of testicular teratomas frequently has genetic abnormalities similar to those of the epithelial components. Concordant chromosome 12p alterations between the fibrous stroma and epithelial elements provide further evidence that both epithelial and fibrous components of teratoma are derived from a common progenitor.
机译:睾丸畸胎瘤通常由多种上皮和基质成分的异质混合物组成。睾丸畸胎瘤纤维基质的生物学性质和遗传特征尚未得到彻底研究。染色体12p异常是生殖细胞肿瘤的标志性遗传改变。我们使用相间荧光原位杂交技术研究了32例纯睾丸畸胎瘤的纤维基质和其他成分中的12p染色体异常。总体而言,纯睾丸畸胎瘤有72%(23/32)具有染色体12p异常。分别在53%(17/32)和41%(13/32)的情况下,在纤维基质中检测到与12p染色体无关的12p或12p过量表达。在等位基因12p阳性的17例病例中,有8例(47%)也存在12p的过高表达。在31%(10/32)的病例中,纤维基质既没有表现出12p的过高表达,也没有显示出12p的同染色体。分别在14/23(61%)和15/23(65%)的胃肠道上皮细胞中发现了等染色体12p和12p的过度表达。在呼吸型上皮中分别占41%(7/17)和41%(7/17)的情况;在鳞状上皮中分别占62%(8/13)和54%(7/13)的情况;在软骨中占63%(5/8)和38%(3/8)的情况。在睾丸畸胎瘤的纤维基质和上皮成分之间观察到一致的染色体12p异常。我们的结果表明,睾丸畸胎瘤的纤维基质经常具有与上皮成分相似的遗传异常。纤维基质与上皮成分之间的一致染色体12p改变提供了进一步的证据,表明畸胎瘤的上皮成分和纤维成分均来自共同的祖细胞。

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