Fang D C, Jass J R, Wang D X
Department of Gastroenterology, 3rd Military Medical University, Southwest Hospital, Chongqing, People's Republic of China.
J Clin Pathol. 1998 Aug;51(8):593-6. doi: 10.1136/jcp.51.8.593.
To investigate the role of DCC gene inactivation in the development and progression of gastric cancer.
Loss of heterozygosity and loss of expression of the DCC gene was studied in 51 surgical specimens of gastric cancer using detection based on polymerase chain reaction.
Loss of heterozygosity was found in 35.3% (18 of 51) of specimens and was detected more often in stage III and IV (50%) than in stage I and II cancers (14.3%) (p < 0.05). Occurrence of loss of heterozygosity was not correlated with histological type, tumour size, depth of invasion, or lymph node metastasis. Loss of expression was found in 49% of cases (25 of 51). Loss of expression was not significantly correlated with any clinicopathological variable.
Loss of heterozygosity and loss of expression of the DCC gene are often encountered in gastric cancer. Loss of heterozygosity of the DCC gene is a late event and associated with malignant progression.
研究DCC基因失活在胃癌发生发展中的作用。
采用基于聚合酶链反应的检测方法,对51例胃癌手术标本进行DCC基因杂合性缺失及表达缺失研究。
35.3%(51例中的18例)标本存在杂合性缺失,Ⅲ期和Ⅳ期(50%)比Ⅰ期和Ⅱ期癌症(14.3%)更常检测到杂合性缺失(p<0.05)。杂合性缺失的发生与组织学类型、肿瘤大小、浸润深度或淋巴结转移无关。49%的病例(51例中的25例)存在表达缺失。表达缺失与任何临床病理变量均无显著相关性。
胃癌中常出现DCC基因杂合性缺失及表达缺失。DCC基因杂合性缺失是一个晚期事件,与恶性进展相关。