Gleeson C M, Sloan J M, McGuigan J A, Ritchie A J, Weber J L, Russell S E
Department of Medical Genetics, The Queen's University of Belfast, Belfast City Hospital, UK.
Br J Cancer. 1997;76(11):1455-65. doi: 10.1038/bjc.1997.578.
To identify chromosomal loci involved in the development of proximal gastric adenocarcinoma, this study delineated the pattern of allelic imbalance in a series of 38 adenocarcinomas arising in the gastric cardia. A total of 137 microsatellite markers covering all autosomal arms, excluding acrocentric arms, were analysed. A mean of 35 out of a total of 39 chromosomal arms studied were informative for each patient. The tumour group demonstrated a high level of allelic imbalance, with an observed median fractional allelic imbalance of 0.47 for the 29 intestinal-type adenocarcinomas and 0.54 for the nine diffuse-type adenocarcinomas. Allelic imbalance was detected in >50% of informative cases in both histological subtypes on a number of chromosomal arms. In the intestinal subtype, these included, 3p (61%), 4q (71%), 5q (59%), 8p (60%), 9p (65%), 9q (83%), 12q (52%), 13q (52%), 17p (78%) and 18q (70%). A higher incidence of allelic imbalance was detected on chromosome 16q in tumours of the diffuse type relative to those of the intestinal type. A more detailed mapping on chromosomes 4q and 6q identified a number of cases with subchromosomal breakpoints. In conclusion, this analysis has indicated regions of the genome potentially involved in the development of proximal gastric carcinomas.
为了确定与近端胃癌发生相关的染色体位点,本研究描绘了一系列38例贲门腺癌中基因不平衡的模式。分析了总共137个覆盖所有常染色体臂(不包括近端着丝粒染色体臂)的微卫星标记。每位患者所研究的总共39条染色体臂中平均有35条具有信息性。肿瘤组显示出高水平的基因不平衡,29例肠型腺癌观察到的中位等位基因不平衡分数为0.47,9例弥漫型腺癌为0.54。在两种组织学亚型的许多染色体臂上,超过50%的信息性病例检测到基因不平衡。在肠型亚型中,这些染色体臂包括3p(61%)、4q(71%)、5q(59%)、8p(60%)、9p(65%)、9q(83%)、12q(52%)、13q(52%)、17p(78%)和18q(70%)。相对于肠型肿瘤,弥漫型肿瘤在染色体16q上检测到更高的基因不平衡发生率。对染色体4q和6q进行更详细的图谱分析发现了一些具有亚染色体断点的病例。总之,该分析表明了基因组中可能与近端胃癌发生相关的区域。