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Àü¸³»ù¾Ï ¼¼Æ÷ÁÖ¿¡¼­ ?-Catenin ¹× Matrix Metalloproteinase-7ÀÇ ¹ßÇö¿¡ ´ëÇÑ DecursinÀÇ È¿°ú Effect of Decursin on the Expression of ?-Catenin and Matrix Metalloproteinase-7 in Prostate Cancer Cell Lines

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ÃÖÀÍÁØ, ¹Î±Ç½Ä, °­µ¿ÀÏ, ¼Û±Ô¿ë, ¿À»óÅÃ,
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ÃÖÀÍÁØ ( Choi Ik-Joon ) 
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç

¹Î±Ç½Ä ( Min Kweon-Sik ) 
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
°­µ¿ÀÏ ( Kang Dong-Il ) 
ÀÎÁ¦´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
¼Û±Ô¿ë ( Song Gyu-Yong ) 
Ãæ³²´ëÇб³ ¾àÇдëÇÐ
¿À»óÅà( Oh Sang-Taek ) 
ÀÎÁ¦´ëÇб³ ¾à¹°À¯Àüü¿¬±¸¼¾ÅÍ

Abstract


Purpose: Alterations in the Wnt/?-catenin pathway are associated with the development and progression of human prostate cancer. Decursin can attenuate the Wnt/?-catenin pathway. We investigated the relationship between the Wnt/?-catenin pathway and decursin in prostate cancer cells.

Materials and Methods: PC-3 and LNCaP cell lines were used. Cell viability was measured with methyl-thiazole tetrazolium bromide(MTT) assays, and cell apoptosis analysis was performed by FACScan. The amount of ?-catenin protein after treatment with decursin was measured by Western blot analysis. Expression of MMP-7 mRNA was detected by real-time polymerase chain reaction(RT-PCR).

Results: Death and apoptosis were increased after treatment with decursin 0.5-100?M in PC-3 and LNCaP cells. This was revealed dose and time-dependent increase of cancer cell death on 24, 48 and 72 hours. FACScan showed an increment of apoptosis on 24, 48 hours. Expression of intracellular ?-catenin protein was decreased dose-dependently in both of prostate cancer cell lines. Decursin reduced MMP-7 mRNA expression on 6, 12, 24, 48 hours dose-dependently.

Conclusions: Decursin affects the viability of prostate cancer cells. Increased cancer cell death was associated with increased apoptosis. This study suggests that decursin may play a role in the treatment of prostate cancer. (Korean J Urol 2009;50:81-88)

Å°¿öµå

Decursin;Beta-catenin;Matrix metalloproteinase;Prostate

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