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Growth Inhibition of Human Lung Carcinoma Cells by ¥â-lapachone through Induction of Apoptosis
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ÀÌÀçÈÆ ( Lee Jae-Hun )
µ¿ÀÇ´ëÇб³ ÇÑÀÇ°ú´ëÇÐ »ýÈÇб³½Ç
¹Úö ( Park Cheol )
µ¿ÀÇ´ëÇб³ ÇÑÀÇ°ú´ëÇÐ »ýÈÇб³½Ç
ÃÖº´ÅÂ ( Choi Byung-Tae )
µ¿ÀÇ´ëÇб³ ÇÑÀÇ°ú´ëÇÐ ÇغÎÇб³½Ç
ÀÌ¿øÈ£ ( Lee Won-Ho )
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ÃÖ¿µÇö ( Choi Yung-Hyun )
µ¿ÀÇ´ëÇб³ ÇÑÀÇ°ú´ëÇÐ »ýÈÇб³½Ç
KMID : 0603520040090010026
Abstract
The DNA topoismerase I inhibitor ¥â-lapachone, the product of a lapacho tree (Tabebuia avellanedae) from South America, activates a novel apoptotic response in a number of cell lines. In the present report, we investigated the effects of ¥â-lapachone on the growth of human lung in human non-small-cell-lung-cancer A549 cells. Upon treatment with ¥â-lapachone, a concentration-dependent inhibition of cell viability and cell proliferation was observed as measured by hemocytometer counts and MTT assay. The ¥â-lapachone- treated cells developed many of the hallmark features of apoptosis, including membrane shrinking, condensation of chromatin and DNA fragmentation. These apoptotic effects of ¥â-lapachone in A549 cells were associated with a marked induction of pro-apoptotic Bax expression, however the levels of anti-apoptotic Bcl-2 expression were decreased in a dose-dependent manner. Accordingly, elevated amount of cyclindependent kinase inhibitor p21 expression accompanied by up-regulation of tumor suppressor p53 was observed. By RT-PCR analyses, decrease in gene expression level of telomerase reverse transcriptase and telomeric repeat binding factor were also observed. Thus, these findings suggest that ¥â-lapachone may be a potential anti-cancer therapeutics for the control of human lung cancer cell model.
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¥â-lapachone ;Lung carcinoma; Apoptosis; Bax; Bcl-2
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