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¥â-Catenin Expression in Gastric Carcinogenesis
°ÇýÀ±, ÃÖ¿¬¶ô, ±èÈ£±Ù,
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°ÇýÀ± ( Kang Hae-Youn )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÃÖ¿¬¶ô ( Choi Yon-Rak )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èÈ£±Ù ( Kim Ho-Guen )
¿¬¼¼´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
KMID : 0357920010350050376
Abstract
Background: The molecular pathogenesis of gastric carcinoma is not yet well characterized. The purpose of this study is to assess the role of ¥â-catenin in gastric carcinogenesis.
Methods: We analyzed ¥â-catenin expression using immunohistochemistry on 68 gastric adenomas and 34 gastric adenocarcinomas, and compared the result with pathological and molecular types of tumors and E-cadherin expression.
Results: Nuclear expression of ¥â-catenin was noted more frequently in gastric adenomas than in carcinomas (40% vs. 21%, 0.05¡Âp<1). There was no significant relationship between nuclear ¥â-catenin expression and histologic degree of adenoma, histologic type of carcinoma or microsatellite instability. E-cadherin expression showed significantly more frequent decrease in the membrane stainability of carcinomas compared to adenomas (p<0.01).
Conclusions: The frequent nuclear ¥â-catenin expression in gastric adenomas suggests that the ¥â-catenin alteration might play an early role in gastric carcinogenesis.
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Stomach neoplasms;Beta catenin;Cadherins;Microsatellite repeats
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