...
首页> 外文期刊>BMC Cancer >Potential role and chronology of abnormal expression of the Deleted in Colon Cancer (DCC) and the p53 proteins in the development of gastric cancer
【24h】

Potential role and chronology of abnormal expression of the Deleted in Colon Cancer (DCC) and the p53 proteins in the development of gastric cancer

机译:结肠癌中的缺失基因(DCC)和p53蛋白异常表达在胃癌发展中的潜在作用和时间顺序

获取原文
           

摘要

Background Loss of activity of tumor suppressor genes is considered a fundamental step in a genetic model of carcinogenesis. Altered expression of the p53 and the Deleted in Colon Cancer (DCC) proteins has been described in gastric cancer and this event may have a role in the development of the disease. According to this hypothesis, we investigated the p53 and the DCC proteins expression in different stages of gastric carcinomas. Methods An immunohistochemical analysis for detection of p53 and DCC proteins expression was performed in tumor tissue samples of patients with UICC stage I and II gastric cancer. For the purpose of the analysis, the staining results were related to the pathologic data and compared between stage categories. Results Ninety-four cases of gastric cancer were analyzed. Disease stage categories were pT1N0 in 23 cases, pT2N0 in 20 cases, pT3N0 in 20 cases and pT1-3 with nodal involvment in 31 cases. Stage pT1-2N0 tumors maintained a positive DCC expression while it was abolished in pT3N0 tumors (p Conclusions Altered expression of both DCC and p53 proteins is detectable in gastric carcinomas. It seems that loss of wild-type p53 gene function and consequent p53 overexpression may be involved in early stages of tumor progression while DCC abnormalities are a late event.
机译:背景技术肿瘤抑制基因的活性丧失被认为是致癌基因模型中的基本步骤。已经在胃癌中描述了p53表达的改变和结肠癌中缺失的(DCC)蛋白的表达,该事件可能在疾病的发展中起作用。根据该假设,我们研究了胃癌不同阶段中p53和DCC蛋白的表达。方法采用免疫组织化学方法检测UICC I期和II期胃癌患者肿瘤组织中p53和DCC蛋白的表达。为了分析的目的,将染色结果与病理数据相关并在阶段分类之间进行比较。结果分析94例胃癌患者。疾病分期为23例pT1N0、20例pT2N0、20例pT3N0和31例涉及淋巴结转移的pT1-3。 pT1-2N0期肿瘤维持DCC阳性表达,而在pT3N0肿瘤中被废除(p结论在胃癌中可检测到DCC和p53蛋白表达的改变。似乎野生型p53基因功能的丧失和随之而来的p53过表达可能参与肿瘤进展的早期阶段,而DCC异常是晚期事件。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号