Title of article :
Anti-proliferative effects of Lethariella zahlbruckneri extracts in human HT-29 human colon cancer cells
Author/Authors :
Ren، نويسنده , , Mei Rong and Hur، نويسنده , , Jae-Seoun and Kim، نويسنده , , Jae Yong and Park، نويسنده , , Kyoung-Wuk and Park، نويسنده , , Seong-Chan and Seong، نويسنده , , Chi-Nam and Jeong، نويسنده , , Il-Yun and Byun، نويسنده , , Myung Woo and Lee، نويسنده , , Mi-Kyung and Seo، نويسنده , , Kwon-Il، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
6
From page :
2157
To page :
2162
Abstract :
This study was performed to elucidate the anti-proliferative effects and the apoptotic mechanisms of extracts from Lethariella zahlbruckneri in HT-29 human colon cancer cells. Both the acetone extract (AEL) and methanolic extract (MEL) of L. zahlbruckneri decreased viable cell numbers in a dose- and time-dependent manner in HT-29 cells. The AEL showed stronger cytotoxicity than MEL. Cell death induced by AEL increased cell populations in the sub-G1 phase, as well as the formation of apoptotic bodies and nuclear condensation, whereas MEL did not. Therefore, the potential of AEL to induce apoptosis was examined. Apoptosis induced by AEL was associated with the activation of initiator caspases-8 and -9, as well as the effector caspase-3. AEL stimulated Bid cleavage. This indicated that the apoptotic action of caspase-8-mediated Bid cleavage leads to the activation of caspase-9. AEL increased the expression of the pro-apoptotic protein, Bax, and decreased the expression of the anti-apoptotic protein, Bcl-2. AEL also increased the expression of the caspase-independent mitochondrial apoptosis factor, AIF, in HT-29 cells. These results indicate that AEL inhibited HT-29 cell proliferation by inducing apoptosis, which might be mediated via both caspase-dependent and -independent pathways.
Keywords :
apoptosis , HT-29 , L. zahlbruckneri , Caspase-dependent and -independent pathway
Journal title :
Food and Chemical Toxicology
Serial Year :
2009
Journal title :
Food and Chemical Toxicology
Record number :
2121222
Link To Document :
بازگشت