위 선종 및 선암에서 Trefoil Factor Family 1 단백의 발현 양상

Expression Pattern of the Trefoil Factor Family 1 in Gastric Adenoma and Carcinoma

  • 박원상 (가톨릭대학교 의과대학 병리학교실) ;
  • 김영실 (가톨릭대학교 의과대학 병리학교실) ;
  • 유남진 (가톨릭대학교 의과대학 병리학교실) ;
  • 박조현 (가톨릭대학교 의과대학 병리학교실 및 외과학교실) ;
  • 유진영 (가톨릭대학교 의과대학 병리학교실) ;
  • 이연수 (가톨릭대학교 의과대학 병리학교실) ;
  • 이정용 (가톨릭대학교 의과대학 병리학교실)
  • Park Won Sang (Departments of Pathology, College of Medicine, The Catholic University of Korea) ;
  • Kim Young Sil (Departments of Pathology, College of Medicine, The Catholic University of Korea) ;
  • Yoo Nam Jin (Departments of Pathology, College of Medicine, The Catholic University of Korea) ;
  • Park Cho Hyun (Departments of Pathology, College of Medicine and Surgery, The Catholic University of Korea) ;
  • Yoo Jin Young (Departments of Pathology, College of Medicine, The Catholic University of Korea) ;
  • Lee Youn Soo (Departments of Pathology, College of Medicine, The Catholic University of Korea) ;
  • Lee Jung Young (Departments of Pathology, College of Medicine, The Catholic University of Korea)
  • 발행 : 2001.03.01

초록

Purpose: The trefoil factor family 1 (TFF1) has a protective effect against gastric mucosal damage induced by nonsteroidal anti-inflammatory drugs or ethanol. In addition, a TFF1 knockout mouse model has exhibited circumferential adenomas with high-grade dysplasia, of which $30\%$ progressed into frankly invasive carcinomas. We tried to determine whether the expression pattern of the TFF1 could be involved in the development of sporadic gastric carcinomas. Materials and Methods: We examined TFF1 expression in a series of 43 sporadic gastric carcinomas and 18 gastric adenomas by immunohistochemistry. Results: Strong positive TFF1 staining was identified primarily in the normal gastric mucosa, mainly in the cytoplasm of the superficial and foveolar epithelium. We found TFF1 expression in $55.8\%$ (24 out of 43) of the gastric carcinomas and in $16.7\%$ (3 out of 18) of the gastric adenomas. Statistically, TFF1 immunoreactivity was significantly higher in diffuse-type ($82.4\%$) than in intestinal-type ($38.5\%$) carcinomas(p=0.0058, Fisher's exact test). Conclusion: Our findings provide sufficient evidence that the expression of TFF1 in gastric cancer may simply disclose gastric-type differentiation of neoplastic cells and provide further support for the existence of at least two pathways of malignant transformation of the gastric mucosa: one via intestinal metaplasia and adenomatous dysplasia, leading to glandular carcinomas with intestinal-type differentiation, and the other via hyperplastic changes or de novo changes, leading to diffuse carcinomas and to a subset of glandular carcinomas displaying gastric-type differentiation.

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