Cytogenetic differences between intestinal and diffuse types of human gastric carcinoma.

K Saal, H P Vollmers, J Müller, J Köhler, H Höhn, H K Müller-Hermelink
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引用次数: 17

Abstract

This study concerns the cytogenetics of 23 gastric carcinomas, classified histologically as intestinal or diffuse types. In carcinomas of the diffuse type, the only numerical changes observed were Y chromosome loss associated with X-chromosome disomy in four of seven male patients. A 46, XX karyotype without recognizable alterations was observed in three of five female patients, and rare structural changes in diffuse carcinomas involved chromosomes 1 and 18. In contrast, intestinal type tumors were exclusively aneuploid, with chromosome modes ranging from 48 to 84. The most consistent change was trisomy 20 in seven of 11 patients, each of which displayed a number of both single and clonal structural aberrations. Frequent structural changes were translocations involving chromosome 13 (including a putative isochromosome 13q in three of 11 patients), and alterations in chromosomes 1, 6 and 12. This study therefore suggests that diffuse and intestinal types of gastric carcinomas do not share a common sequence of genetic changes. The tumor with the worse prognosis (diffuse type) is surprisingly diploid, with uniform X-disomy in both males and females. The clinically less aggressive tumors (intestinal type) show multiple changes, both numerical and structural, of which some are reminiscent of changes seen in tumors of the lower gastrointestinal tract. Cytogenetics may thus be a valuable adjunct in establishing the diagnosis, classification, and prognosis of gastric carcinomas.

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肠型和弥漫型人胃癌的细胞遗传学差异。
本研究涉及23例胃癌的细胞遗传学,组织学上分为肠型或弥漫型。在弥漫性癌中,7例男性患者中有4例观察到的唯一数值变化是与x染色体二体相关的Y染色体丢失。在5名女性患者中,有3名患者的核型为46,xx,没有可识别的改变,弥漫性癌中罕见的结构改变涉及1号和18号染色体。相反,肠型肿瘤完全是非整倍体,染色体模式从48到84不等。最一致的变化是在11名患者中有7名患者的20三体,每个患者都显示出一些单克隆和克隆结构畸变。常见的结构改变是13号染色体易位(包括11例患者中3例推定的同工染色体13q),以及1、6和12号染色体的改变。因此,这项研究表明,弥漫型和肠型胃癌不具有共同的遗传改变序列。预后较差的肿瘤(弥漫性)令人惊讶地是二倍体,在男性和女性中都具有均匀的x二体。临床上侵袭性较低的肿瘤(肠型)表现出多种变化,包括数量和结构上的变化,其中一些与下胃肠道肿瘤的变化相似。因此,细胞遗传学可能是建立胃癌的诊断、分类和预后的有价值的辅助手段。
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