About
"CAM-Cancer" is the name of a project entitled "Concerted Action for Complementary and Alternative Medicine Assessment in the Cancer Field" (CAM-Cancer). Originally funded by the European Commission (EC) within the Framework 5 Programme, it is now hosted by the National Information Center for Complementary and Alternative Medicine (NIFAB) at the University of Tromsø, Norway.
Written by Helen Cooke, Helen Seers and the CAM-Cancer Consortium.
Updated September 21, 2011

Co-enzyme Q10

  • Abstract and key points
  • What is it?
  • Does it work?
  • Is it safe?
  • Download as PDF
  • Printable version
  • View article in one page

What is it?

Scientific/common names

Coenzyme Q10 is also known as: CoQ10, Q10, vitamin Q10, Ubiquinone, Ubidecarenone, Mitoquinone, Adelir, Heartcin, Neuquinone, Taidecanone and 2, 3 dimethoxy-5 methyl-6-decaorenyl benzoquinone.

Ingredients

Coenzyme Q10 is produced naturally by the body. In terms of dietary intake, CoQ10 is found in meat, fatty fish (for instance, sardines and mackerel), whole-grain cereals, brown rice, pasta, wholemeal bread, soya products, nuts and also vegetables (especially broccoli and spinach). Commercially, CoQ10 is made by fermenting beets and sugar cane with yeast.

Application and dosage

CoQ10 is sold as a dietary supplement and is usually administered by mouth as a pill (capsule or tablet), however, CoQ10 can also be given intravenously. According to proponents, manufacturers and providers, doses range from 50mg a day for maintenance to 400mg a day for “therapeutic” effects. The observed safety level (OSL) is 1200mg/day/person 54.

Claims of efficacy / mechanisms of action / alleged indication

A “coenzyme” is a molecule that is necessary for the proper functioning of an enzyme. The “Q” refers to the quinone chemical group and “10” is a particular type of quinone. In the human body, CoQ10 is part of the chain reaction necessary for energy production in cells. As well as this, some researchers class CoQ10 as an antioxidant 2 as it is believed to protect against excess free radicals which are thought to be implicated in tumour development. CoQ10 is also claimed to be an immunostimulant, however, this is based on not more than one study showing increases of IgG levels 3. CoQ10 is found in most tissues; however the liver, heart, kidneys and pancreas hold the highest concentrations and the lungs the lowest 4. Levels of CoQ10 are found to decrease with age. This is due to a decrease in mitochondrial CoQ10 content 5. Investigations also suggest lower tissue levels in people with heart disease 6 and cancer 1,9. Due to this finding, researchers have started to investigate whether CoQ10 could be useful in treating diseases such as cancer.

A study concluded that CoQ10 concentrations were significantly lower in melanoma patients than in a control group. Patients in whom metastases developed in this study had lower levels of CoQ10 than those who did not develop metastases 1,47. Observational studies have reported reduced levels of CoQ10 in diseased breast tissue, but it is not clear if this is simply part of the bodies natural response to cancer 50.

A 2010 cohort study concluded that higher CoQ10 levels in post-menopausal women may be associated with an increased risk of breast cancer 55. A further prospective study reported an inverse relationship between circulating CoQ10 levels and breast cancer risk. The authors propose that a possible explanation of the opposing results is that women at either extreme of CoQ10 levels may be at an increased risk for breast cancer. Both studies are consistent in that women with circulating CoQ10 levels in the range of 500-800 ng/mL have the lowest risk if developing breast cancer 56. The results of a multi-ethnic cohort study suggest that moderate levels of circulating CoQ10 may be optimal for the reduction of prostate cancer risk, but the findings were not statistically significant 57.

At present it is unclear how and whether levels of CoQ10 alter when people are ill, therefore it is unknown if supplementation is necessary at all. Clinical and pre-clinical studies suggest that it helps protect the heart from toxic damage caused by the chemotherapy anthracycline. Although there has been concern that CoQ10 may interfere with the anticancer effects of anthracyclines, as it protects the heart from toxic damage, it is thought that higher doses of anthracycline may be able to be given which could enhance the anticancer effect of the chemotherapy 51.

According to proponents of CoQ10, there are three main potential benefits for taking it as a supplement: a) it may be an anti-cancer agent, b) it may support the body, lessening the toxic effects of chemotherapy and c) it may alleviate chronic fatigue.

Prevalence

In terms of prevalence of the use of the use of CoQ10, it is widely used in Japan, with government approval in relation to cardiovascular disease treatment 7. CoQ10 is also used in Europe 8 and North America 7, with the majority of CoQ10 products being provided by Japanese manufacturers 7.

Legal issues

Coenzyme Q10 is classed as a nutraceutical and therefore suppliers can only advertise in terms of health improving properties instead of medical claims 7.

Cost(s) and expenditure

A good quality CoQ10 supplement can cost between 20 and 70 Euros for 60 capsules. Since there are no clear guidelines on dosage and length of treatment, it is not possible to give an overall cost.

« Abstract and key points
Does it work? »

Citation

Helen Cooke, Helen Seers, CAM-Cancer Consortium. Co-enzyme Q10 [online document]. http://www.cam-cancer.org/layout/set/print/CAM-Summaries/Dietary-approaches/Co-enzyme-Q10. September 21, 2011.

Document history

Most recent revision and update in September 2011 by Helen Cooke.
Fully revised and updated in August 2009 by Helen Cooke.
First published in 2005, authored by by Helen Seers and Helen Cooke.

References

  1. Folkers, K, Osterborg, A, Nylander, M, Morita, M, & Mellstedt, H. Activities of vitamin Q10 in animal models and a serious deficiency in patients with cancer. Biochemical and Biophysical Research Communications. 1997; 234 (2): 296-9.
  2. Frei B, Kim MC, Ames BN. Ubiquinol-10 is an effective lipid-soluble antioxidant at physiological concentrations. Proceedings of the Natural Academy of Science.1990; 87(12):4879-83.
  3. Folkers, K, Shizukuishi, S, Takemura, K, Drzewoski, J, Richardson, P, Ellis, J, & Kuzell, WC. Increase in levels of IgG in serum of patients treated with coenzyme Q10. Research Communication in Chemical Patholology and Pharmacology. 1982; 38 (2): 335-8.
  4. Ernster, L, & Forsmark-Andrée, P. Ubiquinol: an endogenous antioxidant in aerobic organisms. Clinical Investigator. 1993; 71 (8 Suppl): S60-5.
  5. Lass A, Kwong L, Sohal RS. Mitochondrial coenzyme Q content and aging. Biofactors.1999; 9(2-4):199-205.
  6. Coenzyme Q10 PDQ. National Cancer Institute. [online]. 20011 [cited 20011 Aug 14]. Available from: URL http://www.cancer.gov/cancertopics/pdq/cam/coenzymeQ10/healthprofessional/allpages
  7. Jellin, JM., (Ed). Natural Medicines Comprehensive Database. 2003; Stockton, California: Therapeutic Research Faculty.
  8. Damkier A, Jensen AB, Rose C. Use of Q10 in cancer patients. Ugeskr Laeger. 1994, 7;156(6):813-8.
  9. Folkers, K. The potential of coenzyme Q 10 (NSC-140865) in cancer treatment. Cancer Chemotherapy Reports. 1974; 24 (4): 19-22.
  10. Folkers, K, Porter, TH, Bertino, JR, & Moroson, B. Inhibition of two human tumor cell lines by antimetabolites of coenzyme Q10. Research Communication in Chemical Pathology and Pharmacology. 1978; 19 (3): 485-90.
  11. Folkers, K, Brown, R, Judy, WV, & Morita, M. Survival of cancer patients on therapy with coenzyme Q10. Biochemical and Biophysical Research Communications. 1993; 192 (1): 241-5.
  12. Lockwood, K, Moesgaard, S, Hanioka, T, & Folkers, K. Apparent partial remission of breast cancer in 'high risk' patients supplemented with nutritional antioxidants, essential fatty acids and coenzyme Q10. Molecular Aspects of Medicine. 1994; 15 (Suppl): s231-40.
  13. Lockwood, K, Moesgaard, S, & Folkers, K. Partial and complete regression of breast cancer in patients in relation to dosage of coenzyme Q10. Biochemical and Biophysical Research Communications. 1994; 199 (3): 1504-8.
  14. Lockwood, K, Moesgaard, S, Yamamoto, T, & Folkers, K. Progress on therapy of breast cancer with vitamin Q10 and the regression of metastases. Biochemical and Biophysical Research Communications. 1995; 212 (1): 172-7.
  15. Shinozawa, S, Gomita, Y, & Araki, Y. Protective effects of various drugs on adriamycin (doxorubicin)-induced toxicity and microsomal lipid peroxidation in mice and rats. Biological and Pharmaceutical Bulletin. 1993; 16 (11): 1114-7.
  16. Shaeffer, J, El-Mahdi. AM, & Nichols, RK. Coenzyme Q10 and adriamycin toxicity in mice. Research Communication in Chemical Patholology and Pharmacology. 1980; 29 (2): 309-15.
  17. Lund, EL, Quistorff, B, Spang-Thomsen, M, & Kristjansen, PE. Effect of radiation therapy on small-cell lung cancer is reduced by ubiquinone intake. Folia Microbiologica (Praha). 1998; 43 (5): 505-6.
  18. Roffe, L, Schmidt, K, & Ernst, E. Efficacy of coenzyme Q10 for improved tolerability of cancer treatments: a systematic review. Journal of Clinical Oncology. 2004; 1;22 (21): 4418-24.
  19. Takimoto, M, Sakurai, T, Kodama, K, Yokoi, H, Suzuki, Y, Enomoto, K, & Okada, N. Protective effect of CoQ10 administration on cardiac toxicity in FAC therapy. Gan To Kagaku Ryoho. 1982; 9(1): 116-21.
  20. Akihama, T, Nakamoto, Y, Shindo, T, Nakayama, Y, & Miura, A. Protective effects of coenzyme Q10 on the adverse reactions of anthracycline antibiotics: using double blind method--with special reference to hair loss] Gan To Kagaku Ryoho. 1983; 10(10): 2125-9.
  21. Okuma, K, Furuta, I, & Ota, K. Protective effect of coenzyme Q10 in cardiotoxicity induced by adriamycin. Gan To Kagaku Ryoho. 1984; 11(3): 502-8.
  22. Lucarelli, G, Angelucci, C, Giardini, G. et al. Ubidecarenone and toxic cardiopathy from antiblastic therapy with daunoblastine. Boll Chim Farm. 1986; 125: S34-S39.
  23. Iarussi, D, Auricchio, U, Agretto, A, Murano, A, Giuliano, M, Casale, F, Indolfi, P, & Iacono, A. Protective effect of coenzyme Q10 on anthracyclines cardiotoxicity: control study in children with acute lymphoblastic leukemia and non-Hodgkin lymphoma. Molecular Aspects of Medicine. 1994; 15 (Suppl): s207-12.
  24. Thibault, A, Samid, D, Tompkins, AC, Figg, WD, Cooper, MR, Hohl, RJ, Trepel, J, Liang, B, Patronas, N, Venzon, DJ, Reed, E, & Myers, CE. Phase 1 study of lovastatin, an inhibitor of the mevalonate pathway, in patients with cancer. Clinical Cancer Research. 1996; 2: 483-91.
  25. Villalba JM, Parrado C, Santos-Gonzalez M, Alcain FJ, Villalba JM, Parrado C et al. Therapeutic use of coenzyme Q10 and coenzyme Q10-related compounds and formulations. [Review] [211 refs]. Expert Opinion on Investigational Drugs 2010; 19(4):535-554.
  26. Baggio, E, Gandini, R, Plancher, AC, Passeri, M, & Carmosino, G. Italian multicenter study on the safety and efficacy of coenzyme Q10 as adjunctive therapy in heart failure. CoQ10 Drug Surveillance Investigators. Molecular Aspects of Medicine. 1994; 15 (Suppl): s287-94.
  27. Feigin, A, Kieburtz, K, Como, P, Hickey, C, Claude, K, Abwender, D, Zimmerman, C, Steinberg, K, & Shoulson, I. Assessment of coenzyme Q10 tolerability in Huntington's disease. Movement Disorders. 1996; 11 (3): 321-3.
  28. Pepping, J. Coenzyme Q10. American Journal of Health System-Pharmacy. 1999; 56 (6): 519-21.
  29. Ernst E, Pittler MH, Wider B, Boddy K. (Eds). The Desktop Guide to Complementary and Alternative Medicine. An Evidence-Based Approach. Edinburgh: Mosby, 2006.
  30. Overvad, K, Diamant, B, Holm, L, Holmer, G, Mortensen, SA, & Stender, S. Coenzyme Q10 in health and disease. European Journal of Clinical Nutrition. 1999; 53 (10): 764-70.
  31. ConsumerLab: Product review: Coenzyme Q10.. [online]. 20011 [cited 20011 Aug 14]. Available from: URL http://www.consumerlab.com/results/coq10.asp
  32. Borek, C. Dietary antioxidants and human cancer. Integrative Cancer Therapies. 2004; 3 (4), 333-341.
  33. Engelsen J, Nielsen JD, Hansen KF. Effect of Coenzyme Q10 and Ginkgo biloba on warfarin dosage in patients on long-term warfarin treatment. A randomized, double-blind, placebo-controlled cross-over trial. Ugeskr Laeger. 2003, 28 ;165(18):1868-71.
  34. Kaikkonen, J, Nyyssonen, K, Tuomainen, TP, Ristonmaa, U, & Salonen, JT. Determinants of plasma coenzyme Q10 in humans. FEBS Letters. 1999; 443 (2): 163-6.
  35. Hoenjet KMJLF, Dagnelie PC, Delaere KPJ, Wijckmans NEG, Zambon JV, Oosterhof GON. Effect of a nutritional supplement containing vitamin E, selenium, vitamin c and coenzyme Q10 on serum PSA in patients with hormonally untreated carcinoma of the prostate: a randomised placebo-controlled study. Eur Urol. 2005 Apr;47(4):433-9; discussion 9-40.
  36. Premkumar VG, Yuvaraj S, Sathish S, Shanthi P, Sachdanandam P. Anti-angiogenic potential of CoenzymeQ10, riboflavin and niacin in breast cancer patients undergoing tamoxifen therapy. Vascul Pharmacol. 2008 Apr-Jun;48(4-6):191-201.
  37. Premkumar VG, Yuvaraj S, Shanthi P, Sachdanandam P. Co-enzyme Q10, riboflavin and niacin supplementation on alteration of DNA repair enzyme and DNA methylation in breast cancer patients undergoing tamoxifen therapy. Br J Nutr. 2008 Dec;100(6):1179-82.
  38. Premkumar VG, Yuvaraj S, Vijayasarathy K, Gangadaran SGD, Sachdanandam P. Effect of coenzyme Q10, riboflavin and niacin on serum CEA and CA 15-3 levels in breast cancer patients undergoing tamoxifen therapy. Biol Pharm Bull. 2007 Feb;30(2):367-70.
  39. Sachdanandam P. Antiangiogenic and hypolipidemic activity of coenzyme Q10 supplementation to breast cancer patients undergoing Tamoxifen therapy. Biofactors. 2008;32(1-4):151-9.
  40. Yuvaraj S, Premkumar VG, Vijayasarathy K, Gangadaran SGD, Sachdanandam P. Ameliorating effect of coenzyme Q10, riboflavin and niacin in tamoxifen-treated postmenopausal breast cancer patients with special reference to lipids and lipoproteins. Clin Biochem. 2007 Jun;40(9-10):623-8.
  41. Yuvaraj S, Premkumar VG, Vijayasarathy K, Gangadaran SGD, Sachdanandam P. Augmented antioxidant status in Tamoxifen treated postmenopausal women with breast cancer on co-administration with Coenzyme Q10, Niacin and Riboflavin. Cancer Chemother Pharmacol. 2008 May;61(6):933-41.
  42. Yuvaraj S, Premkumar VG, Shanthi P, Vijayasarathy K, Gangadaran SGD, Sachdanandam P. Effect of Coenzyme Q(10), Riboflavin and Niacin on Tamoxifen treated postmenopausal breast cancer women with special reference to blood chemistry profiles. Breast Cancer Res Treat. 2009 Mar;114(2):377-84.
  43. Perumal SS, Shanthi P, Sachdanandam P. Augmented efficacy of tamoxifen in rat breast tumorigenesis when gavaged along with riboflavin, niacin, and CoQ10: effects on lipid peroxidation and antioxidants in mitochondria. Chem Biol Interact. 2005 Feb 28;152(1):49-58.
  44. Perumal SS, Shanthi P, Sachdanandam P. Combined efficacy of tamoxifen and coenzyme Q10 on the status of lipid peroxidation and antioxidants in DMBA induced breast cancer. Mol Cell Biochem. 2005 May;273(1-2):151-60.
  45. Sakano K, Takahashi M, Kitano M, Sugimura T, Wakabayashi K. Suppression of azoxymethane-induced colonic premalignant lesion formation by coenzyme Q10 in rats. Asian Pac J Cancer Prev. 2006 Oct-Dec;7(4):599-603.
  46. Rusciani L, Proietti I, Paradisi A, Rusciani A, Guerriero G, Mammone A, et al. Recombinant interferon alpha-2b and coenzyme Q10 as a postsurgical adjuvant therapy for melanoma: a 3-year trial with recombinant interferon-alpha and 5-year follow-up. Melanoma Res. 2007 Jun;17(3):177-8
  47. Rusciani L, Proietti I, Rusciani A, Paradisi A, Sbordoni G, Alfano C, et al. Low plasma coenzyme Q10 levels as an independent prognostic factor for melanoma progression. J Am Acad Dermatol. 2006 Feb;54(2):234-41
  48. van Dalen EC, Caron HN, Dickinson HO, Kremer LC, van Dalen EC, Caron HN et al. Cardioprotective interventions for cancer patients receiving anthracyclines.[Update of Cochrane Database Syst Rev. 2008;(2):CD003917; PMID: 18425895]. Cochrane Database of Systematic Reviews 2011; 6:CD003917.
  49. Nicolson GL, Conklin KA. Reversing mitochondrial dysfunction, fatigue and the adverse effects of chemotherapy of metastatic disease by molecular replacement therapy. Clin Exp Metastasis. 2008;25(2):161-9.
  50. Coenzyme Q10 PDQ. Natural Standard Database. [online].2009 [cited 2009 May 31]. Available from URL http://www.naturalstandard.com/naturalstandard/monographinfo.asp?title=Coenzyme%20Q10&file=coenzymeq10
  51. Conklin, K. A. (2005). "Coenzyme q10 for prevention of anthracycline-induced cardiotoxicity." Integrative Cancer Therapies 4(2): 110-30.
  52. Bryant, J., J. Picot, et al. (2007)"Cardioprotection against the toxic effects of anthracyclines given to children with cancer: a systematic review." Health Technology Assessment (Winchester, England) 11(27): ii
  53. Hidaka, J, Fujii, K, et al. (2008) Safety assessment of Coenzyme Q10 (CoQ10). Biofactors 32(1-4): 499-508.
  54. Hathcock, J, Shao, (2006) A Risk Assessment for CoenzymeQ10(Ubiquinone). Regul Toxicol Pharm 45(3): 282-288.
  55. Chai W, Cooney RV, Franke AA, Shvetsov YB, Caberto CP, Wilkens LR et al. Plasma coenzyme Q10 levels and postmenopausal breast cancer risk: the multiethnic cohort study. Cancer Epidemiology, Biomarkers & Prevention 2010; 19(9):2351-2356.
  56. Cooney RV, Dai Q, Gao YT, Chow WH, Franke AA, Shu XO et al. Low plasma coenzyme q10 levels and breast cancer risk in chinese women. Cancer Epidemiology, Biomarkers & Prevention 2011; 20(6):1124-1130.
  57. Chai W, Cooney RV, Franke AA, Caberto CP, Wilkens LR, Le ML et al. Plasma coenzyme Q10 levels and prostate cancer risk: the multiethnic cohort study. Cancer Epidemiology, Biomarkers & Prevention 2011; 20(4):708-710.
  58. Chandran K, Aggarwal D, Migrino RQ, Joseph J, McAllister D, Konorev EA et al. Doxorubicin inactivates myocardial cytochrome c oxidase in rats: cardioprotection by Mito-Q. Biophysical Journal 2009; 96(4):1388-1398
  59. Fouad AA, Al-Sultan AI, Refaie SM, Yacoubi MT, Fouad AA, Al-Sultan AI et al. Coenzyme Q10 treatment ameliorates acute cisplatin nephrotoxicity in mice. Toxicology 2010; 274(1-3):49-56.
Legal notice
The present documentation has been compiled by the CAM-CANCER Project with all due care and expert knowledge. However, the CAM-CANCER Project provides no assurance, guarantee or promise with regard to the correctness, accuracy, up-to-date status or completeness of the information it contains. This information is designed for health professionals. Readers are strongly advised to discuss the information with their physician. Accordingly, the CAM-CANCER Project shall not be liable for damage or loss caused because anyone relies on the information.