Microsatellite instability in solitary and sporadic gastric cancer.

Revista do Hospital das Clinicas Pub Date : 2004-10-01 Epub Date: 2004-10-29 DOI:10.1590/s0041-87812004000500010
Rodrigo Oliva Perez, Carlos Eduardo Jacob, Fabricio L'ofreddo D'Ottaviano, Conrado Alvarenga, Adriana Safatle Ribeiro, Ulysses Ribeiro, Cláudio José Caldas Bresciani, Bruno Zilberstein, José Eduardo Krieger, Angelita Habr-Gama, Joaquim José Gama-Rodrigues
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引用次数: 21

Abstract

Unlabelled: Recently, the presence of microsatellite instability (MSI) has been reported in gastric cancer and associated with older age of presentation, distal tumor location, early disease staging, and better overall prognosis. Different characteristics in presentation and in tumor behavior may be explained by different genetic alterations during carcinogenesis of gastric cancer. Identification of specific genetic pathways in gastric cancer may have direct impact on prognosis and selection of treatment strategies.

Patients and methods: All 24 patients were treated by radical surgery. Fragments of normal and tumor tissues were extracted from the specimen and stored at -80 degrees C before DNA purification and extraction. PCR amplification utilizing microsatellite markers was performed. Tumors presenting PCR products of abnormal sizes were considered positive for microsatellite instability (MSI+).

Results: Five patients (21%) had tumors that were MSI+ in at least 1 marker. In the group of patients with Lauren's intestinal-type gastric carcinoma, 3 had tumors that were MSI+ (23%), while in the group of diffuse-type gastric cancer, 2 patients had tumors that were MSI+ (19%). The mean age of presentation and the male:female ratio was similar in both groups. Tumors that were MSI+ were more frequently located in proximal portion of the stomach compared to microsatellite-stable (MSS) tumors (40% vs. 16%). Although there was a trend of patients with MSI+ tumors towards a proximal gastric tumor location, early staging, and negative lymph node metastasis, there was no statistical significance compared to those with MSS tumors (P >.1). Comparison of overall and disease-free survival between gastric tumors that were MSI+ and those that were MSS found no statistically significant differences (P >.1).

Conclusions: Microsatellite instability is a frequent event in gastric carcinogenesis and shows a trend towards distinct clinical and pathological characteristics of gastric cancer.

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孤立和散发性胃癌的微卫星不稳定性。
未标记:最近,微卫星不稳定性(MSI)在胃癌中的存在被报道,并与年龄较大、肿瘤远端位置、早期疾病分期和更好的整体预后相关。胃癌发生过程中不同的基因改变可能解释其表现和肿瘤行为的不同特征。胃癌特异性遗传通路的确定可能直接影响预后和治疗策略的选择。患者及方法:24例患者均行根治性手术治疗。从标本中提取正常组织和肿瘤组织片段,在-80℃保存,然后进行DNA纯化和提取。利用微卫星标记进行PCR扩增。出现异常大小PCR产物的肿瘤被认为是微卫星不稳定性(MSI+)阳性。结果:5例患者(21%)的肿瘤在至少1项标志物上为MSI+。Lauren氏肠型胃癌组3例肿瘤为MSI+(23%),弥漫性胃癌组2例肿瘤为MSI+(19%)。两组患者的平均发病年龄和男女比例相似。与微卫星稳定(MSS)肿瘤相比,MSI+肿瘤更常位于胃近端(40%对16%)。虽然MSI+肿瘤患者有向胃近端肿瘤位置、早期分期、淋巴结转移阴性的趋势,但与MSS肿瘤患者相比,差异无统计学意义(P > 1)。MSI+组与MSS组的总生存期和无病生存期比较,差异无统计学意义(P > 1)。结论:微卫星不稳定性是胃癌发生过程中常见的事件,具有胃癌独特的临床和病理特征。
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