The contribution of activating transcription factor 3 to apoptosis of human colorectal cancer cells by Protocatechualdehyde, a naturally occurring phenolic compound

被引:13
作者
Lee, Jeong Rak [1 ]
Lee, Man Hyo [1 ]
Eo, Hyun Ji [2 ]
Park, Gwang Hun [2 ]
Song, Hun Min [2 ]
Kim, Mi Kyoung [2 ]
Lee, Jin Wook [2 ]
Jeong, Jin Boo [2 ,3 ]
机构
[1] Gyeongbuk Inst Bioind, Andong 760380, South Korea
[2] Andong Natl Univ, Dept Bioresource Sci, Andong 760749, South Korea
[3] Andong Natl Univ, Inst Agr Sci & Technol, Andong 760749, South Korea
关键词
Protocatechualdehyde; Chemoprevention; Colorectal cancer; Activating transcription factor 3; Apoptosis; ADAPTIVE-RESPONSE GENE; CYCLIN D1; PROSTATE-CANCER; FACTOR ATF3; EXPRESSION; 3,4-DIHYDROXYBENZALDEHYDE; ANTIOXIDANT; TEA;
D O I
10.1016/j.abb.2014.10.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protocatechualdehyde (PCA) is one of the important compounds found in barley, green cavendish bananas and grapevine leaves. PCA shows anti-cancer activities in breast, leukemia and colorectal cancer cells. Previous study reported that PCA exerts anti-cancer activity through down-regulating cyclin D1 and HDAC2 in human colorectal cancer cells. However, the underlying mechanisms for the expression of activating transcription factor 3 (ATF3) by PCA has not been studied. Thus, we performed in vitro study to investigate if treatment of PCA affects ATF3 expression and ATF3-mediated apoptosis in human colorectal cancer cells. PCA decreased cell viability in a dose-dependent manner in HCT116 and SW480 cells. In addition, PCA reduced cell viability in MCF-7, MDA-MB-231 and HepG-2 cells. Exposure of PCA activated the levels of ATF3 protein and mRNA in HCT116 and SW480 cells. Inhibition of ERK1/2/ by PD98059 and p38 by SB203580 inhibited PCA-induced ATF3 expression and transcriptional activation. ATF3-knockdown inhibited PCA-induced apoptosis and cell viability. In addition, ATF3 overexpression enhanced PCA-mediated cleavage of PARP. These findings suggest that inhibition of cell viability and apoptosis by PCA may be result of ATF3 expression through ERK1/2 and p38-mediated transcriptional activation. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
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