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1,1-Bis(3′-indolyl)-1-(p-methoxyphenyl)methane activates Nur77-independent proapoptotic responses in colon cancer cells : 1,1-Bis(3'-indolyl)-1-(<i>p</i>-methoxyphenyl)methane activates Nur77-independent proapoptotic responses in colon cancer cells

Cited 23 time in Web of Science Cited 22 time in Scopus
Authors

Cho, Sung Dae; Lei, Ping; Abdelrahim, Maen; Yoon, Kyungsil; Liu, Shengxi; Guo, Jingjing; Papineni, Sabitha; Chintharlapalli, Sudhakar; Safe, Stephen

Issue Date
2008-04
Publisher
John Wiley & Sons Inc.
Citation
Molecular Carcinogenesis, Vol.47 No.4, pp.252-263
Abstract
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.
ISSN
0899-1987
URI
https://hdl.handle.net/10371/208984
DOI
https://doi.org/10.1002/mc.20378
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Research Area Discovery of molecular targets related to oral cancer metastasis and identification of signal transduction system, Identifying the role of immunological tolerance in oral cancer, Presenting a new concept oral cancer prevention and treatment strategy through identification of major molecular targets and mechanisms related to oral cancer development, 구강암 발병관련 주요 분자표적 및 기전 규명을 통한 신개념 구강암 예방 및 치료전략 제시, 구강암 전이관련 분자표적 발굴 및 신호전달체계 규명, 구강암에서 면연관용의 역할 규명

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