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Ann Thorac Surg 2001;71:949-954
© 2001 The Society of Thoracic Surgeons
a Second Department of Surgery, Kagawa Medical University, Kagawa, Japan
b Department of Pathology, Kagawa Medical University, Kagawa, Japan
Accepted for publication October 18, 2000.
Address reprint request to Dr Yokomise, Second Department of Surgery, Kagawa Medical University, 1750-1, Miki-cho, Kita-gun, Kagawa 761-0793, Japan
e-mail: yokomise{at}kms.ac.jp
Background. E-Cadherin plays a major role in maintaining the intercellular junctions in epithelial tissues. The reduction of E-cadherin expression in cancer cells may be associated with tumor differentiation, metastasis, and a poor prognosis.
Methods. Immunohistochemistry for E-cadherin expression was performed on 109 tumors from patients with nonsmall cell lung cancer who underwent operations.
Results. With respect to membranous immunostaining, 57 carcinomas were E-cadherin-positive, 39 carcinomas E-cadherin-reduced, and 13 carcinomas E-cadherin-negative. The percentage of poorly differentiated tumors in the impaired E-cadherin expression group was significantly higher than that in the E-cadherin-positive group (p = 0.005). Furthermore, the frequency of lymph node metastases in tumors with impaired E-cadherin expression was significantly higher than that in the E-cadherin-positive tumors (p = 0.011). A Cox regression analysis revealed that E-cadherin expression was a significant factor in the prediction of survival for patients with nonsmall cell lung cancer (p = 0.002).
Conclusions. E-Cadherin expression was associated with tumor differentiation, lymph node metastasis, and prognosis in patients with nonsmall cell lung cancer.
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