Consumption of the putative chemopreventive agent curcumin by cancer patients: assessment of curcumin levels in the colorectum and their pharmacodynamic consequences - PubMed (original) (raw)
Affiliations
- PMID: 15668484
Clinical Trial
Consumption of the putative chemopreventive agent curcumin by cancer patients: assessment of curcumin levels in the colorectum and their pharmacodynamic consequences
Giuseppe Garcea et al. Cancer Epidemiol Biomarkers Prev. 2005 Jan.
Abstract
Curcumin, a constituent of the spice turmeric, has been shown to reduce the adenoma burden in rodent models of colorectal cancer accompanied by a reduction of levels of the oxidative DNA adduct 3-(2-deoxy-beta-di-erythro-pentafuranosyl)-pyr[1,2-alpha]-purin-10(3H)one (M(1)G) and of expression of the enzyme cyclooxygenase-2 (COX-2). We tested the hypothesis that pharmacologically active levels of curcumin can be achieved in the colorectum of humans as measured by effects on levels of M(1)G and COX-2 protein. Patients with colorectal cancer ingested curcumin capsules (3,600, 1,800, or 450 mg daily) for 7 days. Biopsy samples of normal and malignant colorectal tissue, respectively, were obtained at diagnosis and at 6 to 7 hours after the last dose of curcumin. Blood was taken 1 hour after the last dose of curcumin. Curcumin and its metabolites were detected and quantitated by high-performance liquid chromatography with detection by UV spectrophotometry or mass spectrometry. M(1)G levels and COX-2 protein expression were measured by immunoslot blot and Western blotting, respectively. The concentrations of curcumin in normal and malignant colorectal tissue of patients receiving 3,600 mg of curcumin were 12.7 +/- 5.7 and 7.7 +/- 1.8 nmol/g, respectively. Curcumin sulfate and curcumin glucuronide were identified in the tissue of these patients. Trace levels of curcumin were found in the peripheral circulation. M(1)G levels were 2.5-fold higher in malignant tissue as compared with normal tissue (P < 0.05 by ANOVA). Administration of curcumin (3,600 mg) decreased M(1)G levels from 4.8 +/- 2.9 adducts per 107 nucleotides in malignant colorectal tissue to 2.0 +/- 1.8 adducts per 107 nucleotides (P < 0.05 by ANOVA). COX-2 protein levels in malignant colorectal tissue were not affected by curcumin. The results suggest that a daily dose of 3.6 g curcumin achieves pharmacologically efficacious levels in the colorectum with negligible distribution of curcumin outside the gut.
Similar articles
- Phase I clinical trial of oral curcumin: biomarkers of systemic activity and compliance.
Sharma RA, Euden SA, Platton SL, Cooke DN, Shafayat A, Hewitt HR, Marczylo TH, Morgan B, Hemingway D, Plummer SM, Pirmohamed M, Gescher AJ, Steward WP. Sharma RA, et al. Clin Cancer Res. 2004 Oct 15;10(20):6847-54. doi: 10.1158/1078-0432.CCR-04-0744. Clin Cancer Res. 2004. PMID: 15501961 Clinical Trial. - Pilot study of oral silibinin, a putative chemopreventive agent, in colorectal cancer patients: silibinin levels in plasma, colorectum, and liver and their pharmacodynamic consequences.
Hoh C, Boocock D, Marczylo T, Singh R, Berry DP, Dennison AR, Hemingway D, Miller A, West K, Euden S, Garcea G, Farmer PB, Steward WP, Gescher AJ. Hoh C, et al. Clin Cancer Res. 2006 May 1;12(9):2944-50. doi: 10.1158/1078-0432.CCR-05-2724. Clin Cancer Res. 2006. PMID: 16675592 - Effects of dietary curcumin on glutathione S-transferase and malondialdehyde-DNA adducts in rat liver and colon mucosa: relationship with drug levels.
Sharma RA, Ireson CR, Verschoyle RD, Hill KA, Williams ML, Leuratti C, Manson MM, Marnett LJ, Steward WP, Gescher A. Sharma RA, et al. Clin Cancer Res. 2001 May;7(5):1452-8. Clin Cancer Res. 2001. PMID: 11350917 - Cyclooxygenase-2 inhibition in colorectal cancer: boom or bust?
Sanborn R, Blanke CD. Sanborn R, et al. Semin Oncol. 2005 Feb;32(1):69-75. doi: 10.1053/j.seminoncol.2004.09.035. Semin Oncol. 2005. PMID: 15726508 Review. - Curcumin as "Curecumin": from kitchen to clinic.
Goel A, Kunnumakkara AB, Aggarwal BB. Goel A, et al. Biochem Pharmacol. 2008 Feb 15;75(4):787-809. doi: 10.1016/j.bcp.2007.08.016. Epub 2007 Aug 19. Biochem Pharmacol. 2008. PMID: 17900536 Review.
Cited by
- EGFR(s) in aging and carcinogenesis of the gastrointestinal tract.
Nautiyal J, Kanwar SS, Majumdar AP. Nautiyal J, et al. Curr Protein Pept Sci. 2010 Sep;11(6):436-50. doi: 10.2174/138920310791824110. Curr Protein Pept Sci. 2010. PMID: 20491625 Free PMC article. Review. - Advances in plant-derived natural products for antitumor immunotherapy.
Yang Y, Liu Q, Shi X, Zheng Q, Chen L, Sun Y. Yang Y, et al. Arch Pharm Res. 2021 Nov;44(11):987-1011. doi: 10.1007/s12272-021-01355-1. Epub 2021 Nov 9. Arch Pharm Res. 2021. PMID: 34751930 Review. - Biochemistry, Safety, Pharmacological Activities, and Clinical Applications of Turmeric: A Mechanistic Review.
Ahmad RS, Hussain MB, Sultan MT, Arshad MS, Waheed M, Shariati MA, Plygun S, Hashempur MH. Ahmad RS, et al. Evid Based Complement Alternat Med. 2020 May 10;2020:7656919. doi: 10.1155/2020/7656919. eCollection 2020. Evid Based Complement Alternat Med. 2020. PMID: 32454872 Free PMC article. Review. - Enhancing the Bioavailability and Bioactivity of Curcumin for Disease Prevention and Treatment.
Bertoncini-Silva C, Vlad A, Ricciarelli R, Giacomo Fassini P, Suen VMM, Zingg JM. Bertoncini-Silva C, et al. Antioxidants (Basel). 2024 Mar 8;13(3):331. doi: 10.3390/antiox13030331. Antioxidants (Basel). 2024. PMID: 38539864 Free PMC article. Review. - Exploring the Contribution of Curcumin to Cancer Therapy: A Systematic Review of Randomized Controlled Trials.
de Waure C, Bertola C, Baccarini G, Chiavarini M, Mancuso C. de Waure C, et al. Pharmaceutics. 2023 Apr 19;15(4):1275. doi: 10.3390/pharmaceutics15041275. Pharmaceutics. 2023. PMID: 37111761 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical
Research Materials