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The Differential Expressions of the Epithelial-Mesenchymal Transition Regulator, Slug and the Cell Adhesion Molecule, E-cadherin in Colorectal Adenocarcinoma

´ëÇѺ´¸®ÇÐȸÁö 2008³â 42±Ç 6È£ p.351 ~ 357
È«¶õ, Choi Dong-Yul, ÀÓ¼ºÃ¶, ¼­ÀçÈ«, ±â±ÙÈ«, À̹ÌÀÚ,
¼Ò¼Ó »ó¼¼Á¤º¸
È«¶õ ( Hong Ran ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

 ( Choi Dong-Yul ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÀÓ¼ºÃ¶ ( Lim Sung-Chul ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
¼­ÀçÈ« ( Suh Chae-Hong ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±â±ÙÈ« ( Kee Keun-Hong ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
À̹ÌÀÚ ( Lee Mi-Ja ) 
Á¶¼±´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

Abstract


Background : Slug is a member of the Snail family of transcription factors, and it plays a crucial role in the regulation of the epithelial-mesenchymal transition by suppression of several epithelial proteins and adhesion molecules, including E-cadherin.

Methods : The aim of the present study was to examine the significance between the expression of Slug in colorectal adenocarcinoma (CRA) specimens and the clinicopathological parameters of CRA, as determined by immunohistochemical analysis, and to determine the correlation between the Slug and E-cadherin expressions in non-neoplastic colorectal mucosa (n=45), primary CRA (n= 109) and metastatic CRA (n=17). A semiquantitative scoring system was applied based on the intensity and extent of the positive immunohistochemical staining.

Results : The expressions of Slug and E-cadherin were associated with the depth of tumor invasion (pT) (p=0.019, p=0.001, respectively), and these expressions showed a significant inverse correlation (p< 0.001) each other.
Conclusions : Our results demonstrated a positive role for Slug in the development of CRA, and Slug is a mediator of tumor invasion in CRA. In addition, an up-regulated Slug expression is significantly correlated with the loss of an E-cadherin expression, which suggests that Slug may play some role in the epithelial-mesenchymal transition (EMT) by down-regulating the E-cadherin expression.

Å°¿öµå

Slug transcription factors; E-cadherin; Colon; Adenocarcinoma; Immunohistochemistry

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