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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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Bioavailability of curcumin: problems and promises.

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Gut Microbiota in Health and Disease

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Curcumin as “Curecumin”: From kitchen to clinic

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Curcumin: From ancient medicine to current clinical trials

TL;DR: Curcumin exhibits great promise as a therapeutic agent, and is currently in human clinical trials for a variety of conditions, including multiple myeloma, pancreatic cancer, myelodysplastic syndromes, colon cancer, psoriasis and Alzheimer’s disease.
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Curcumin: The story so far

TL;DR: Sufficient data currently exist to advocate phase II clinical evaluation of oral curcumin in patients with invasive malignancy or pre-invasive lesions of the gastrointestinal tract, particularly the colon and rectum.
References
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Curcumin inhibition of bleomycin-induced pulmonary fibrosis in rats

TL;DR: Findings suggest curcumin as a potent anti‐inflammatory and anti‐fibrotic agent against BLM‐induced pulmonary fibrosis in rats.
Journal Article

The inhibitory effect of curcumin, genistein, quercetin and cisplatin on the growth of oral cancer cells in vitro.

TL;DR: It is concluded that curcumin is considerably more potent than genistein and quercetin, but cisplatin is five fold more potent in inhibition of growth and DNA synthesis in SCC-25.
Journal Article

Curcumin Inhibits Tyrosine Kinase Activity of p185neu and Also Depletes p185neu

TL;DR: Because curcumin effectively inhibited p 185neu tyrosine kinase activity by depleting p185neu and potently suppressed the growth of multiple breast cancer cell lines, its therapeutic potential in advanced breast cancer is worthy of further investigation.
Journal Article

Hepatocellular carcinoma results from chronic cyclin D1 overexpression in transgenic mice.

TL;DR: It is demonstrated that overexpression of cyclin D1 is sufficient to initiate hepatocellular carcinogenesis and these animals represent a unique and significant new model for the study of human HCC.
Journal Article

Curcumin induced modulation of cell cycle and apoptosis in gastric and colon cancer cells.

TL;DR: In both cell lines, immunoblot analysis indicated that curcumin caused induction of apoptosis as evidenced by cleavage of PARP, caspase-3, and reduction in Bcl-XL levels.
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