摘要
为了明确胃癌的血液或淋巴转移和微卫星DNA不稳定性(Microsateliteinstability,MSI)及杂合性缺失(Lossofheterozygosity,LOH)的关系,选择29个多态微卫星DNA标记(MS),采用PCR-聚丙烯酰胺凝胶电泳及银染技术,分析了38例胃癌的MSI和LOH频率。其中胃癌伴有血液或淋巴转移的24例;不伴有血液或淋巴转移的14例,结果表明:总的MSI和LOH频率分别为20.84%和27.59%,伴有血液或淋巴转移的胃癌,MSI在D7S520、D8S279位点频率最高为54.17%;LOH在D6S430位点频率最高为62.50%。无血液或淋巴转移的胃癌,MSI和LOH频率均为57.1%。经χ2检验,LOH和MSI的发生频率在伴有或不伴有血液或淋巴转移胃癌中,两者无统计学差异。表明胃癌的血液或淋巴转移和MSI及LOH的发生频率无关,目前还难以以这两个指标作为辅助性的判断预后。
In order to identify the effects of MSI(Microsatellite instability, MSI) and LOH(Loss of heterozygosity, LOH) in gastric cancer metastasis, we selected 29 Microsatellite markers to analyse 38 cases with (24 patients) or without (14 patients) lymphatic permeation for their MSI and LOH. The highest rate of MSI at D7S520 and D8S279 was 54.17%, and the highest rate of LOH at D6S430 was 62.50% in gastric cancer with metastasis. The highest rate of LOH and MSI at D3S1067 in gastric cancer without metastasis was 57.14%. There was no significant difference between them. We think that MSI and LOH can not be used as the indicators of malignant degree and prognosis of gastric cancer.
出处
《肿瘤研究与临床》
CAS
1997年第4期218-221,共4页
Cancer Research and Clinic
关键词
微卫生
DNA
胃肿瘤
血液
肿瘤转移
Gastric cancer Microsatellite instability Loss of heterozygosity Metastasis DNA