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Anticancer potential of curcumin: preclinical and clinical studies.

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TLDR
Evidence has also been presented to suggest that curcumin can suppress tumor initiation, promotion and metastasis, and Pharmacologically,Curcumin has been found to be safe.
Abstract
Curcumin (diferuloylmethane) is a polyphenol derived from the plant Curcuma longa, commonly called turmeric. Extensive research over the last 50 years has indicated this polyphenol can both prevent and treat cancer. The anticancer potential of curcumin stems from its ability to suppress proliferation of a wide variety of tumor cells, down-regulate transcription factors NF- κB, AP-1 and Egr-1; down-regulate the expression of COX2, LOX, NOS, MMP-9, uPA, TNF, chemokines, cell surface adhesion molecules and cyclin D1; down-regulate growth factor receptors (such as EGFR and HER2); and inhibit the activity of c-Jun N-terminal kinase, protein tyrosine kinases and protein serine/threonine kinases. In several systems, curcumin has been described as a potent antioxidant and anti-inflammatory agent. Evidence has also been presented to suggest that curcumin can suppress tumor initiation, promotion and metastasis. Pharmacologically, curcumin has been found to be safe. Human clinical trials indicated no dose-limiting toxicity when administered at doses up to 10 g/day. All of these studies suggest that curcumin has enormous potential in the prevention and therapy of cancer. The current review describes in detail the data supporting these studies. Curcumin, derived from turmeric (vernacular name: Haldi), is a rhizome of the plant Curcuma longa. The medicinal use of this plant has been documented in Ayurveda (the Indian

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Citations
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DNA interaction studies of a novel Cu(II) complex as an intercalator containing curcumin and bathophenanthroline ligands.

TL;DR: It is found that the copper(II) complex can cleave puC18 DNA and induces detectable changes in the CD spectrum of CT-DNA, a decrease in absorption spectrum, and an increase in its viscosity.
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Spectrometric Study on the Interaction of Dodecyltrimethylammonium Bromide with Curcumin

TL;DR: The interaction between dodecyltrimethylammonium bromide and curcumin has been studied in pH 5.0 sodium phosphate buffer using absorption and fluorescence measurements and the values of anisotropy and microviscosity ofCurcumin obtained from the fluorescence polarization technique showed pronounced changes at different surfactant concentrations.
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Application of Nanoparticles on Diagnosis and Therapy in Gliomas

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Targeting events in melanoma carcinogenesis for the prevention of melanoma

TL;DR: The data for several promising agents, including statins, curcumin, resveratrol, silymarin and green tea, are reviewed, and some importance issues and concepts that should be considered in any melanoma chemoprevention strategy are discussed.
Journal ArticleDOI

Effect of different oleogelators on lipolysis and curcuminoid bioaccessibility upon in vitro digestion of sunflower oil oleogels

TL;DR: Upon in vitro digestion, fatty acid release as a function of digestion time was greatly affected by oleogel structure: the extent of lipolysis decreased as oleogiel strength increased and CUs bioaccessibility was lower in Oleogels containing crystalline particles (MG and RW).
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Journal Article

Phase I clinical trial of curcumin, a chemopreventive agent, in patients with high-risk or pre-malignant lesions.

TL;DR: It is demonstrated that curcumin is not toxic to humans up to 8,000 mg/day when taken by mouth for 3 months and a biologic effect ofCurcumin in the chemoprevention of cancer is suggested.
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Transcriptional regulation of endothelial cell adhesion molecules: NF-kappa B and cytokine-inducible enhancers.

TL;DR: A model has been proposed for the cytokine‐induced E‐selectin enhancer that is similar to the stereospecific complex proposed forThe inter‐ feron‐β gene promoter, in which multiple DNA bending proteins facilitate the assembly of higher order complexes of transcriptional activators that interact as a unit with the basal transcriptional machinery.
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Influence of Piperine on the Pharmacokinetics of Curcumin in Animals and Human Volunteers

TL;DR: The study shows that in the dosages used, piperine enhances the serum concentration, extent of absorption and bioavailability of curcumin in both rats and humans with no adverse effects.
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