Saal K, Vollmers H P, Müller J, Köhler J, Höhn H, Müller-Hermelink H K
Pathologisches Institut, Universität Würzburg, Germany.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(3):145-50. doi: 10.1007/BF02915107.
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.
本研究涉及23例胃癌的细胞遗传学,这些胃癌在组织学上分为肠型或弥漫型。在弥漫型癌中,观察到的唯一数量变化是7例男性患者中有4例出现Y染色体丢失并伴有X染色体双体。5例女性患者中有3例观察到核型为46,XX且无明显改变,弥漫型癌中罕见的结构变化涉及1号和18号染色体。相比之下,肠型肿瘤均为非整倍体,染色体众数范围为48至84。最一致的变化是11例患者中有7例出现20号染色体三体,每例均显示出一些单条和克隆性结构畸变。常见的结构变化是涉及13号染色体的易位(包括11例患者中有3例出现假定的13q等臂染色体),以及1号、6号和12号染色体的改变。因此,本研究表明,弥漫型和肠型胃癌不存在共同的遗传变化序列。预后较差的肿瘤(弥漫型)令人惊讶地为二倍体,男性和女性均有一致的X双体。临床上侵袭性较小的肿瘤(肠型)显示出数量和结构上的多种变化,其中一些让人联想到下消化道肿瘤中所见的变化。因此,细胞遗传学在胃癌的诊断、分类和预后判定中可能是一项有价值的辅助手段。