Ottini L, Palli D, Falchetti M, D'Amico C, Amorosi A, Saieva C, Calzolari A, Cimoli F, Tatarelli C, De Marchis L, Masala G, Mariani-Costantini R, Cama A
Department of Oncology and Neurosciences, University Gabriele D'Annunzio, Chieti, Italy.
Cancer Res. 1997 Oct 15;57(20):4523-9.
We studied the presence of microsatellite instability (MSI) in a series of 108 gastric cancers (GCs) previously identified in an epidemiological study carried out in a high-risk area around Florence. To investigate associations between MSI and GC family history, 34 cases (31.5%) who had a GC-affected first-degree relative were included in the series. A family history positive for colorectal cancer was reported quite rarely (5.6%). The analysis of 6 microsatellite loci in DNA from paired normal tissue and tumor samples microdissected from paraffin-embedded specimens revealed varying degrees of instability: 56 cases (51.8%) did not show instability at any of the 6 loci; 19 (17.6%) showed instability at 1 locus; 16 (14.8%) showed instability at 2 loci; 11 (10.2%) showed instability at 3 loci; 4 (3.7%) showed instability at 4 loci; and 2 (1.9%) showed instability at 5 loci. The replication error-positive (RER+) phenotype, defined as the presence of MSI at 2 or more loci, had a frequency of 30.6% (33 of 108) and tended to be positively associated with female sex, intestinal histological type, advanced tumor stage, vascular invasion, positive GC family history, and blood group of A type. No correlation emerged between age at diagnosis and RER+ phenotype, whereas a significant association with the RER+ phenotype was shown by the antral location. A multivariate analysis adjusting for a selected group of potential confounding factors confirmed the strong association of the RER+ phenotype with the antral location (P = 0.001) and with a positive GC family history (P < 0.05). Survival analyses at 5 and 8 years showed no difference between RER+ and RER- patients, even when corrected for stage distribution. By the microdissection technique, we also used microsatellite allele patterns to investigate intratumoral heterogeneity and genetic relationships between tumors and adjacent dysplasia and/or intestinal metaplasia. Areas of metaplasia and dysplasia demonstrated MSI only in cases with MSI-positive tumors. In MSI-positive tumors, there was consistent evidence of intratumoral microsatellite allele heterogeneity, indicating the presence of genetically divergent tumor cell clones within the same neoplasm.
我们研究了在佛罗伦萨周边高风险地区进行的一项流行病学研究中先前鉴定出的108例胃癌(GC)中微卫星不稳定性(MSI)的存在情况。为了调查MSI与GC家族史之间的关联,该系列纳入了34例(31.5%)有受GC影响的一级亲属的病例。报告有结直肠癌家族史阳性的情况非常罕见(5.6%)。对从石蜡包埋标本中显微切割的配对正常组织和肿瘤样本的DNA中的6个微卫星位点进行分析,发现了不同程度的不稳定性:56例(51.8%)在6个位点中的任何一个位点均未显示不稳定性;19例(17.6%)在1个位点显示不稳定性;16例(14.8%)在2个位点显示不稳定性;11例(10.2%)在3个位点显示不稳定性;4例(3.7%)在4个位点显示不稳定性;2例(1.9%)在5个位点显示不稳定性。复制错误阳性(RER+)表型定义为在2个或更多位点存在MSI,其频率为30.6%(108例中的33例),并且倾向于与女性性别、肠型组织学类型、肿瘤晚期、血管侵犯、GC家族史阳性和A型血型呈正相关。诊断年龄与RER+表型之间未发现相关性,而胃窦部位置与RER+表型显示出显著关联。对一组选定的潜在混杂因素进行校正的多变量分析证实了RER+表型与胃窦部位置(P = 0.001)和GC家族史阳性(P < 0.05)之间的强关联。5年和8年的生存分析显示RER+和RER-患者之间没有差异,即使校正了分期分布也是如此。通过显微切割技术,我们还使用微卫星等位基因模式来研究肿瘤内异质性以及肿瘤与相邻发育异常和/或肠化生之间的遗传关系。化生和发育异常区域仅在MSI阳性肿瘤的病例中显示MSI。在MSI阳性肿瘤中,有一致的证据表明肿瘤内微卫星等位基因异质性,表明在同一肿瘤内存在基因不同的肿瘤细胞克隆。