1,1-Bis(3'-indolyl)-1-(p-methoxyphenyl)methane activates Nur77-independent proapoptotic responses in colon cancer cells

被引:25
作者
Cho, Sung Dae [2 ,3 ,4 ]
Lei, Ping [2 ]
Abdelrahim, Maen [2 ]
Yoon, Kyungsil [2 ]
Liu, Shengxi [2 ]
Guo, Jingjing [2 ]
Papineni, Sabitha [2 ]
Chintharlapalli, Sudhakar [2 ]
Safe, Stephen [1 ,2 ]
机构
[1] Texas A&M Univ, Dept Vet Physiol & Pharmacol, College Stn, TX 77843 USA
[2] Texas A&M Univ, Hlth Sci Ctr, Inst Biosci & Technol, Houston, TX USA
[3] Chonbuk Natl Univ, Sch Dent, Dept Oral Pathol, Jeonju, South Korea
[4] Chonbuk Natl Univ, Inst Oral Biosci, Jeonju, South Korea
关键词
C-DIMS; NAG-1; apoptosis; JNK; colon cancer;
D O I
10.1002/mc.20378
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
1,1-Bis(3'-indolyl)-1-(p-methoxyphenyl)methane (DIM-C-pPhOCH(3)) is a methylene-substituted diindolylmethane (C-DIM) analog that activates the orphan receptor nerve growth factor-induced-B alpha (NGFI-B alpha, Nur77). RNA interference studies with small inhibitory RNA for Nur77 demonstrate that DIM-C-pPhOCH3 induces Nur77-dependent and -independent apoptosis, and this study has focused on delineating the Nur77-independent proapoptotic pathways induced by the C-DIM analog. DIM-C-pPhOCH3 induced caspase-dependent apoptosis in RKO colon cancer cells through decreased mitochondrial membrane potential which is accompanied by increased mitochondrial bax/bcl-2 ratios and release of cytochrome c into the cytosol. DIM-C-pPhOCH3 also induced phosphatidylinositol-3-kinase-dependent activation of early growth response gene-1 which, in turn, induced expression of the proapoptotic nonsteroidal anti-inflammatory drug-activated gene-1 (NAG1) in RKO and SW480 colon cancer cells. Moreover, DIM-C-pPhOCH3 also induced NAG-1 expression in colon tumors in athymic nude mice bearing RKO cells as xenografts. DIM-C-pPhOCH3 also activated the extrinsic apoptosis pathway through increased phosphorylation of c-jun N-terminal kinase which, in turn, activated C/EBP homologous transcription factor (CHOP) and death receptor 5 (DR5). Thus, the effectiveness of DIM-C-pPhOCH3 as a tumor growth inhibitor is through activation of Nur77-dependent and -independent pathways. (C) 2007 Wiley-Liss, Inc.
引用
收藏
页码:252 / 263
页数:12
相关论文
共 49 条
[1]
3,3′-Diindolylmethane (DIM) and its derivatives induce apoptosis in pancreatic cancer cells through endoplasmic reticulum stress-dependent upregulation of DR5 [J].
Abdelrahim, M ;
Newman, K ;
Vanderlaag, K ;
Samudio, I ;
Safe, S .
CARCINOGENESIS, 2006, 27 (04) :717-728
[2]
Molecular cloning and characterization of human nonsteroidal anti-inflammatory drug-activated gene promoter - Basal transcription is mediated by Sp1 and Sp3 [J].
Baek, SJ ;
Horowitz, JM ;
Eling, TE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) :33384-33392
[3]
Differential expression of NGFI-B and RNR-1 genes in various tissues and developing brain of the rat: Comparative study by quantitative reverse transcription-polymerase chain reaction [J].
Bandoh, S ;
Tsukada, T ;
Maruyama, K ;
Ohkura, N ;
Yamaguchi, K .
JOURNAL OF NEUROENDOCRINOLOGY, 1997, 9 (01) :3-8
[4]
Aryl hydrocarbon receptor-mediated antiestrogenic and antitumorigenic activity of diindolylmethane [J].
Chen, I ;
McDougal, A ;
Wang, F ;
Safe, S .
CARCINOGENESIS, 1998, 19 (09) :1631-1639
[5]
1,1-bis(3′-indolyl)-1-(p-substitutedphenyl) methanes are peroxisome proliferator-activated receptor γ agonists but decrease HCT-116 colon cancer cell survival through receptor-independent activation of early growth response-1 and nonsteroidal anti-inflammatory drug-activated gene-1 [J].
Chintharlapalli, S ;
Papineni, S ;
Baek, SJ ;
Liu, SX ;
Safe, S .
MOLECULAR PHARMACOLOGY, 2005, 68 (06) :1782-1792
[6]
Activation of Nur77 by selected 1,1-bis(3'-indolyl)-1-(p-substituted phenyl) methanes induces apoptosis through nuclear pathways [J].
Chintharlapalli, S ;
Burghardt, R ;
Papineni, S ;
Ramaiah, S ;
Yoon, K ;
Safe, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (26) :24903-24914
[7]
1,1-bis(3′-indolyl)-1-(p-substitutedphenyl)methanes induce peroxisome proliferator-activated receptor γ-mediated growth inhibition, transactivation, and differentiation markers in colon cancer cells [J].
Chintharlapalli, S ;
Smith, R ;
Samudio, I ;
Zhang, W ;
Safe, S .
CANCER RESEARCH, 2004, 64 (17) :5994-6001
[8]
1,1-bis(3′-indolyl)-1-(p-substitutedphenyl)methanes inhibit growth, induce apoptosis, and decrease the androgen receptor in LNCaP prostate cancer cells through peroxisome proliferator-activated receptor γ-independent pathways [J].
Chintharlapalli, Sudhakar ;
Papineni, Sabitha ;
Safe, Stephen .
MOLECULAR PHARMACOLOGY, 2007, 71 (02) :558-569
[9]
Nur77 agonists induce proapoptotic genes and responses in colon cancer cells through nuclear receptor-dependent and nuclear receptor-in dependent pathways [J].
Cho, Sung Dae ;
Yoon, Kyungsil ;
Chintharlapalli, Sudhakar ;
Abdelrahim, Maen ;
Lei, Ping ;
Hamilton, Stanley ;
Khan, Shaheen ;
Ramaiah, Shashi K. ;
Safe, Stephen .
CANCER RESEARCH, 2007, 67 (02) :674-683
[10]
A novel ring-substituted diindolylmethane, 1,1-bis[3′-(5-methoxyindolyl)]-1-(p-t-butylphenyl) methane, inhibits extracellular signal-regulated kinase activation and induces apoptosis in acute myelogenous leukemia [J].
Contractor, R ;
Samudio, IJ ;
Estrov, Z ;
Harris, D ;
McCubrey, JA ;
Safe, SH ;
Andreeff, M ;
Konopleva, M .
CANCER RESEARCH, 2005, 65 (07) :2890-2898