Kim Hyung-Seok, Lee Ji-Shin, Freund Jean-Noel, Min Kyung-Whan, Lee Jeong-Soo, Kim Wan, Juhng Sang-Woo, Park Chang-Soo
Department of Pathology, Seonam University, College of Medicine, Korea.
J Gastroenterol Hepatol. 2006 Feb;21(2):438-42. doi: 10.1111/j.1440-1746.2005.03933.x.
Recent studies have demonstrated that CDX-2 is expressed in the intestinal metaplasia of the stomach and intestinal-type gastric cancer. To address the role of CDX-2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX-2 in gastric carcinoma and precursor lesions were examined using immunohistochemistry.
A total of 160 specimens diagnosed as gastric carcinomas or non-invasive neoplasia from 158 patients were analyzed for CDX-2 expression by immunochemical methods. Patients were classified into histopathologic subgroups according to the Padova international classification: 60 cases of low-grade non-invasive neoplasia, 55 cases of high grade, and 45 cases of invasive intestinal-type adenocarcinoma. The CDX-2 expression in non-neoplastic gastric mucosa including intestinal metaplasia was also evaluated in the areas included in the histologic sections.
The CDX-2 expression was localized in the epithelial cell nuclei in the area of intestinal metaplasia with or without dysplasia and carcinoma, consistent with its role as a transcriptional regulator. No CDX-2 reactivity was noted in the normal mucosa in all cases. The CDX-2 expression was detected in 73.3% of low-grade cases, 85.5% of high-grade cases and 91.1% of intestinal-type adenocarcinoma cases. In the gastric mucosa with intestinal metaplasia, 89.7% of the samples were positive. The CDX-2-expressing cells in intestinal metaplasia were more prevalent than in dysplasia and carcinoma. Expression of CDX-2 showed a statistically significant positive correlation with increasing grade of dysplasia and carcinoma.
These findings suggest that CDX-2 expression in stomach cancer may be a marker of the progression of gastric carcinogenesis, and that its activation may represent an early event.
近期研究表明,CDX-2在胃肠化生及肠型胃癌中表达。为探讨CDX-2在肠型胃癌发生中的作用,采用免疫组化法检测了CDX-2在胃癌及癌前病变中的表达。
采用免疫化学方法分析了158例患者的160份诊断为胃癌或非侵袭性肿瘤的标本中CDX-2的表达。根据帕多瓦国际分类将患者分为组织病理学亚组:60例低级别非侵袭性肿瘤、55例高级别肿瘤和45例侵袭性肠型腺癌。还对组织学切片所包含区域的非肿瘤性胃黏膜(包括肠化生)中的CDX-2表达进行了评估。
CDX-2表达定位于有或无异型增生及癌的肠化生区域的上皮细胞核中,与其作为转录调节因子的作用一致。所有病例的正常黏膜均未发现CDX-2反应性。低级别病例中73.3%检测到CDX-2表达,高级别病例中为85.5%,肠型腺癌病例中为91.1%。在有肠化生的胃黏膜中,89.7%的样本呈阳性。肠化生中CDX-2表达细胞比异型增生和癌中更普遍。CDX-2表达与异型增生和癌的分级增加呈统计学显著正相关。
这些发现表明,胃癌中CDX-2表达可能是胃癌发生进展的标志物,其激活可能代表早期事件。