유방암 환자에서 E-cadherin의 발현 및 임상적 의의
- Alternative Title
- Expression of E-cadherin and Clinical Correlation in Patients with Breast Carcinoma
- Abstract
- PURPOSE: E-cadherin is a Ca (2+)-dependent cell adhesion molecule that plays an important role in normal growth and development via the mediation of homotypic, homophilic cell-cell interactions. Recent studies suggest that E-cadherin may also be important in neoplastic progression, particularly as a suppressor of invasion. METHODS: To evaluate the expression of E-cadherin, according to the histopathological features and the relation between E-cadherin and prognosis in breast carcinoma, immunohistochemical staining, using mouse HECD-1 was performed for 66 cases of breast carcinoma. RESULTS: The breast carcinomas showed loss or marked reduction of E-cadherin expression in 42 (63.6%) of the 66 cases. In a multivariate analysis, E-cadherin expression had no independent prognostic value, while the axillary lymph node status, tumor diameter, and TNM stage were independent prognostic factors. The results indicate that E-cadherin expression was related to several histological features in breast cancer, but had no independent prognostic value over standard prognostic factors. No significant correlation was found between E-cadherin expression and tumor size, stage, nuclear grade, lymph node status, histologic type, or hormonal status. CONCLUSION: The loss or marked reduction of E-cadherin expression in breast carcinomas was not related to the prog nosis of the patients.
- All Author(s)
- J. M. Kim
; T. Y. Kim
; D. Song
; S. Y. Kim
; M. J. Baek
; M. S. Lee
; C. H. Kim
; S. H. Yang
; M. H. Lee
; M. S. Cho
- Intsitutional Author(s)
- 김성용; 백무준; 이문수
- Issued Date
- 2004
- Type
- Article
- Keyword
- Breast Cancer; E-Cadherin
- Publisher
- 한국유방암학회
Korean Breast Cancer Society
- ISSN
- 1598-3641
- Citation Title
- Journal of Korean Breast Cancer Society
- Citation Volume
- 7
- Citation Number
- 3
- Citation Start Page
- 148
- Citation End Page
- 153
- Language(ISO)
- kor
- DOI
- 10.4048/jkbcs.2004.7.3.148
- URI
- http://schca-ir.schmc.ac.kr/handle/2022.oak/4633
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