Literature DB >> 21703360

Attenuation of multi-targeted proliferation-linked signaling by 3,3'-diindolylmethane (DIM): from bench to clinic.

Sanjeev Banerjee1, Dejuan Kong, Zhiwei Wang, Bin Bao, Gilda G Hillman, Fazlul H Sarkar.   

Abstract

Emerging evidence provide credible support in favor of the potential role of bioactive products derived from ingesting cruciferous vegetables such as broccoli, brussel sprouts, cauliflower and cabbage. Among many compounds, 3,3'-diindolylmethane (DIM) is generated in the acidic environment of the stomach following dimerization of indole-3-carbinol (I3C) monomers present in these classes of vegetables. Both I3C and DIM have been investigated for their use in preventing, inhibiting, and reversing the progression of cancer - as a chemopreventive agent. In this review, we summarize an updated, wide-ranging pleiotropic anti-tumor and biological effects elicited by DIM against tumor cells. It is unfeasible to point one single target as basis of cellular target of action of DIM. We emphasize key cellular and molecular events that are effectively modulated in the direction of inducing apoptosis and suppressing cell proliferation. Collectively, DIM orchestrates signaling through Ah receptor, NF-κB/Wnt/Akt/mTOR pathways impinging on cell cycle arrest, modulation of key cytochrome P450 enzymes, altering angiogenesis, invasion, metastasis and epigenetic behavior of cancer cells. The ability of DIM to selectively induce tumor cells to undergo apoptosis has been observed in preclinical models, and thus it has been speculated in improving the therapeutic efficacy of other anticancer agents that have diverse molecular targets. Consequently, DIM has moved through preclinical development into Phase I clinical trials, thereby suggesting that DIM could be a promising and novel agent either alone or as an adjunct to conventional therapeutics such as chemo-radio and targeted therapies. An important development has been the availability of DIM formulation with superior bioavailability for humans. Therefore, DIM appears to be a promising chemopreventive agent or chemo-radio-sensitizer for the prevention of tumor recurrence and/or for the treatment of human malignancies.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21703360      PMCID: PMC4120774          DOI: 10.1016/j.mrrev.2011.06.001

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  142 in total

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2.  3,3'-diindolylmethane (DIM) and its derivatives induce apoptosis in pancreatic cancer cells through endoplasmic reticulum stress-dependent upregulation of DR5.

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Journal:  Carcinogenesis       Date:  2005-12-06       Impact factor: 4.944

3.  Activation of caspase-8 contributes to 3,3'-Diindolylmethane-induced apoptosis in colon cancer cells.

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Journal:  Nat Rev Drug Discov       Date:  2006-08       Impact factor: 84.694

5.  3,3'-Diindolylmethane downregulates pro-survival pathway in hormone independent prostate cancer.

Authors:  Venkata P S Garikapaty; Badithe T Ashok; Kiranmayi Tadi; Abraham Mittelman; Raj K Tiwari
Journal:  Biochem Biophys Res Commun       Date:  2005-12-20       Impact factor: 3.575

6.  Quantitative combination effects between sulforaphane and 3,3'-diindolylmethane on proliferation of human colon cancer cells in vitro.

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10.  Induction of G1 and G2/M cell cycle arrests by the dietary compound 3,3'-diindolylmethane in HT-29 human colon cancer cells.

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  42 in total

1.  Diindolylmethane-mediated Gli1 protein suppression induces anoikis in ovarian cancer cells in vitro and blocks tumor formation ability in vivo.

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2.  Selective Aryl Hydrocarbon Receptor Modulator 3,3'-Diindolylmethane Impairs AhR and ARNT Signaling and Protects Mouse Neuronal Cells Against Hypoxia.

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Journal:  Mol Neurobiol       Date:  2015-10-17       Impact factor: 5.590

3.  Leucine signaling in the pathogenesis of type 2 diabetes and obesity.

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Journal:  World J Diabetes       Date:  2012-03-15

Review 4.  Targeted regulation of PI3K/Akt/mTOR/NF-κB signaling by indole compounds and their derivatives: mechanistic details and biological implications for cancer therapy.

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Journal:  Anticancer Agents Med Chem       Date:  2013-09       Impact factor: 2.505

5.  Epigenetic modifications of Nrf2 by 3,3'-diindolylmethane in vitro in TRAMP C1 cell line and in vivo TRAMP prostate tumors.

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6.  2,3,7,8-Tetrachlorodibenzo-p-dioxin has both pro-carcinogenic and anti-carcinogenic effects on neuroendocrine prostate carcinoma formation in TRAMP mice.

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7.  Dietary diindolylmethane suppresses inflammation-driven lung squamous cell carcinoma in mice.

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Review 8.  The Role of Nutraceuticals in Pancreatic Cancer Prevention and Therapy: Targeting Cellular Signaling, MicroRNAs, and Epigenome.

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9.  Regulators of gene expression as biomarkers for prostate cancer.

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Review 10.  Epigenetic modifications by dietary phytochemicals: implications for personalized nutrition.

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