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Induction of Selective Cell Death of Oral Squamous Carcinoma Cells by Integrin ¥á2 Antibody and EGFR Antibody

Maxillofacial Plastic and Reconstructive Surgery 2013³â 35±Ç 3È£ p.143 ~ 154
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ÃÖ¿¬½Ä ( Choi Yeon-Sik ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç
Ȳ´ë¼® ( Hwang Dae-Seok ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç
½Å»óÈÆ ( Shin Sang-Hun ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç
±è¿í±Ô ( Kim Uk-Kyu ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç
±è±Ôõ ( Kim Gyoo-Cheon ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø ±¸°­ÇغÎÇб³½Ç
À±½Ä ( Yoon Sik ) - ºÎ»ê´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ÇغÎÇб³½Ç
±èöÈÆ ( Kim Chul-Hoon ) - µ¿¾Æ´ëÇб³ ÀÇ°ú´ëÇÐ ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç
Àü¿µÂù ( Jeon Yeong-Chan ) - ºÎ»ê´ëÇб³ Ä¡ÀÇÇÐÀü¹®´ëÇпø º¸Ã¶Çб³½Ç
º¯ÁØÈ£ ( Byun June-Ho ) - °æ»ó´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ±¸°­¾Ç¾È¸é¿Ü°úÇб³½Ç

Abstract


Purpose: This study was to find efficacy of integrin alpha2 (${\alpha}_2$ ¼ö½Ä À̹ÌÁö) and epidermal growth factor receptor (EGFR) as tumor marker of oral squamous cell carcinoma (SCC) and clarify the selective cell death effect of anti-integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö and anti-EGFR on SCC cells, additionally testify conjugated gold nanoparticles (GNP) with air plasma for selective cell death of oral SCC.

Methods: Expression of integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, EGFR on human SCC cells (SCC25) were examined by western blot. SCC25 cells were treated with anti-integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, anti-EGFR and analysed by Hemacolor staining, immunoflorescence staining, FACS flow cytometry. Conjugated GNP with integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, EGFR antibody were treated by air plasma on SCC cells.

Results: Integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö and EGFR were over-expressed on SCC25 cells than normal lung WI-38 cells. The cell viability rate of SCC25 cells treated with anti-integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, anti-EGFR was lower than WI-38 cells. The concentration changes of nucleus, releasing cytochrome c and apoptosis inducing factor (AIF) from mitochondria to cytosol were observed. The changes of proteins related with apoptosis were observed. Increase of bax, bcl-xL, activation of caspase-3, -7, -9, and fragmentation of PARP, DFF45 and decrease of lamin A/C in SCC25 cells were observed. In FACS, increase of sub-$G_1$ ¼ö½Ä À̹ÌÁö and S phase was observed. Cell cycle related proteins, Such as cyclin D1, cyclin dependent kinase (CDK) 4, cyclin A, cyclin E, CDK 2, p27 were decreased. After SCC25 cells treated with conjugatged GNP-Integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, GNP-EGFR, additionally air plasma, the cell death rate was significantly increased.

Conclusion: Integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, EGFR were over-expressed in oral SCC cells. Anti-integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, anti-EGFR in SCC25 cells induced apoptosis selectively. When GNP-anti integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, GNP-anti EGFR were treated with air plasma on SCC25 cells, cancer cells were died more selectively. GNP-anti integrin ${\alpha}_2$ ¼ö½Ä À̹ÌÁö, GNP-anti EGFR with air plasma could be treatment choice of oral SCC.

Å°¿öµå

OSCC;Integrin alpha2;EGFR;Gold nanoparticles;Cell death

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