CancerNetwork Members: Login | Register
CancerNetwork SearchMedica Medline Drugs

Powered by SearchMedica

 
PUBLICATIONS
NEWS
PODCASTS
TOPICS
BLOGS
NURSES
PATIENTS
JOBS
CONFERENCES
CME
SUPPLEMENTS
 

Home » Integrative Oncology

ONCOLOGY. Vol. 25 No. 14
INTEGRATIVE ONCOLOGY 

Green Tea (Camellia sinensis)

Complementary Therapies, Herbs, and Other OTC Agents

By Guest Editor Barrie Cassileth, PhD1 | December 31, 2011
1Laurance S. Rockefeller Chair and Chief, Integrative Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York

ALSO KNOWN AS: Chinese tea, green tea extract, green tea polyphenols, epigallocatechin gallate (EGCG).

BACKGROUND: Green tea, derived from the leaves of Camellia sinensis, is consumed widely in Asia. Originally cultivated in East Asia, the plant is now grown in the Middle East and in some parts of Africa. Green tea has gained global popularity over the last few decades.

The leaves used to produce green tea are unfermented. They are steamed or heated immediately following harvest. This minimizes oxidation of the polyphenols, which are compounds that act as antioxidants and are thought to confer the health benefits attributed to green tea.

Green tea has been used in traditional medicine as a stimulant, as a diuretic, for wound healing, to promote digestion, and to improve heart health. More recently, green tea and its extracts have been used to prevent and treat hyperlipidemia, hypertension, atherosclerosis, and cancer.

Green tea is available as a dietary supplement in capsule form, as an extract, and in ointments for external application.

TAKE HOME POINTS
• Green tea, popular in China for over 4,000 years, enjoys a worldwide reputation for conferring a variety of health benefits.
• Evidence of the chemopreventive potential of green tea is limited to preclinical and epidemiologic studies.
• Green tea extract can interact with many prescription drugs. Because of its antioxidant effects, green tea extract may also affect chemotherapy and radiotherapy.

For additional information, visit the Memorial Sloan-Kettering Cancer Center Integrative Medicine Service website, “About Herbs,” at http://www.mskcc.org/AboutHerbs.

RESEARCH: The active constituent of green tea extract is EGCG, which accounts for 40% of its total polyphenol content. Regular consumption of green tea may reduce the risk of hypertension[1] and positively affect mood.[2] It also enhances glucose tolerance in healthy individuals[3] but did not improve insulin sensitivity or glycemic control in those with type 2 diabetes.[4] Green tea also may reduce mortality due to cardiovascular disease in both men and women.[5] Topical application of green tea extracts was shown to be effective against external genital and perianal warts.[6] A green tea extract, sinecatechin, used for genital warts, is an FDAapproved drug.

Several pre-clinical, case-control and prospective cohort studies show that green tea has chemopreventive properties.[7-9] However, a metaanalysis of epidemiologic studies failed to find that green tea prevents stomach cancer.[10] The FDA recently concluded that green tea is unlikely to reduce the risk of breast or prostate cancer.[11] Randomized clinical trials, currently underway, may help resolve the uncertainty surrounding the anticancer potential of green tea.

ADVERSE REACTIONS: Several cases of hepatitis have been associated with consumption of green tea.[12-14] A 40-year-old woman developed pruritic swelling and darkening of the lower lip following use of green tea for several years. Symptoms resolved after she discontinued consumption of green tea. [15] A 38-year-old woman developed thrombotic thrombocytopenic purpura following green tea supplementation for weight loss.[16]

Animal studies indicate that oral consumption of green tea extract while fasting can increase the risk of toxicity.[17]

HERB-DRUG INTERACTIONS: Anticoagulants/ antiplatelets: Theoretically, consumption of large amounts of green tea (0.5–1.0 gallon/day) may provide enough vitamin K to antagonize the effects of anticoagulants and antiplatelet agents, although this effect has not been reported in humans.[18]

Bortezomib (Velcade): EGCG and other polyphenols in green tea can inhibit the therapeutic effect of bortezomib(Drug information on bortezomib) and other boronic acid–based proteasome inhibitors.[19]

Tamoxifen: EGCG was shown to increase the oral bioavailability of tamoxifen(Drug information on tamoxifen).[20]

Verapamil: The bioavailability of verapamil(Drug information on verapamil) increased significantly in the presence of EGCG, an effect thought to be due to P-glycoprotein inhibition by EGCG.[21]

Irinotecan: A study found EGCG to inhibit the transport of irinotecan(Drug information on irinotecan) and its metabolite SN-38 into biliary elimination, resulting in prolongation of their half-life, which can increase toxicity.[22]

Cytochrome P450 3A4 substrates: Green tea extract inhibits CYP3A4 and can affect the intracellular concentration of drugs metabolized by this enzyme.[12]

UGT (uridine 5'-diphospho-glucuronosyltransferase) substrates: Green tea modulates UGT enzymes in vitro and can increase the side effects of drugs metabolized by them.

 

Join the Conversation

Want to join the conversation? If you're a healthcare professional, we'd like to hear your comments. Just sign in or register today to become part of our growing, online community.





REFERENCES

1.Yang YC, et al. The protective effect of habitual tea consumption on hypertension. Arch Intern Med. 2004;164:1534-40.

2. Brown AL, Lane J, Coverly J, et al. Effects of dietary supplementation with the green tea polyphenol epigallocatechin-3-gallate on insulin resistance and associated metabolic risk factors: randomized controlled trial. Br J Nutr. 101:886-94.

3. Venables MC, Hulston CJ, Cox HR, Jeukendrup AE. Green tea extract ingestion, fat oxidation, and glucose tolerance in healthy humans. Am J Clin Nutr. 2008;87:778-84.

4. Mackenzie T, Leary L, Brooks WB. The effect of an extract of green and black tea on glucose control in adults with type 2 diabetes mellitus: double-blind randomized study. Metabolism. 2007;56:1340-4.

5. Kuriyama S, Shimazu T, Ohmori K, et al. Green tea consumption and mortality due to cardiovascular disease, cancer, and all causes in Japan: the Ohsaki study. JAMA. 2006;296:1255-65.

6. Stockfleth E, Beti H, Orasan R, et al. Topical polyphenon E in the treatment of external genital and perianal warts: a randomized controlled trial.Br J Dermatol. 2008;158:1329-38.

7. Pisters KM, Newman RA, Coldman B, et al. Phase I trial of oral green tea extract in adult patients with solid tumors. J Clin Oncol. 2001;19:1830-8.

8. Sun CL, Yuan JM, Lee MJ, et al. Urinary tea polyphenols in relation to gastric and esophageal cancers: a prospective study of men in Shanghai, China. Carcinogenesis 2002;23:1497-503.

9. Tsao AS, Liu D, Martin J, et al. Phase II randomized, placebo-controlled trial of green tea extract in patients with high-risk oral premalignant lesions. Cancer Prev Res (Phila Pa). 2009;2:931-41.

10. Myung SK, Bae WK, Oh SM, et al. Green tea consumption and risk of stomach cancer: a meta-analysis of epidemiologic studies. Int J Cancer. 2009;124:670-7.

11. Letter from FDA. Green tea and cancer. Available from: http://www.fda.gov/Food/LabelingNutrition/LabelClaims/QualifiedHealthClaims/ucm073992.htm#gtea. Issued February 24, 2011. Accessed October 18, 2011.

12. Mazzanti G, Menniti-Ippolito F, Moro PA, et al. Hepatotoxicity from green tea: a review of the literature and two unpublished cases. Eur J Clin Pharmacol. 2009;65:331-41.

13. Vanstraelen S, Rahier J, Geubel AP. Jaundice as a misadventure of a green tea (Camellia sinensis) lover : a case report. Acta Gastroenterol Belg. 2008;71:409-12.

14. Verhelst X, Burvenich P, Van Sassenbroeck D, et al. Acute hepatitis after treatment for hair loss with oral green tea extracts (Camellia sinensis). Acta Gastroenterol Belg. 2009;72:262-4.

15. Lee JI, Cho BK, Ock SM, Park HJ. Pigmented contact cheilitis: from green tea? Contact Dermatitis. 2010;62:60-1.

16. Liatsos GD, Moulakakis A, Ketikoglou I, Klonari S. Possible green tea-induced thrombotic thrombocytopenic purpura. Am J Health Syst Pharm. 2010;67:531-4.

17. Wu KM. Green tea extract induced lethal toxicity in fasted but not in nonfasted dogs. Int J Toxicol. 2010;(1):19-20

18. Taylor JR, Wilt VM. Probable antagonism of warfarin by green tea. Ann Pharmacother 1999;33:426-8.

19. Goldin EB, Lam P, Kardosh A, et al. Green tea polyphenols block the anticancer effects of bortezomib and other boronic acid based proteasome inhibitors. Blood. 2009;113:5927-37.

20. Shin SC, Choi JS. Effects of epigallocatechin gallate on the oral bioavailability and pharmacokinetics of tamoxifen and its main metabolite, 4-hydroxytamoxifen, in rats. Anticancer Drugs. 2009;20:584-8.

21. Chung JH, Choi DH, Choi JS. Effects of oral epigallocatechin gallate on the oral pharmacokinetics of verapamil in rats. Biopharm Drug Dispos. 2009;30:90-3.

22. Lin LC, Wang MN, Tsai TH. Food-drug interaction of (-)-epigallocatechin-3-gallate on the pharmacokinetics of irinotecan and the metabolite SN-38. Chem Biol Interact. 2008;174:177-82.

23. Mohamed ME, Frye RF. Effects of herbal supplements on drug glucuronidation. Review of clinical, animal, and in vitro studies. Planta Med. 2011;77:311-21.


 
RELATED CONTENT

Physical Activity Across the Cancer Continuum
ONCOLOGY,  June 18, 2013
Exercise After Cancer Diagnosis: Time to Get Moving
ONCOLOGY,  June 18, 2013
The Role of Physical Activity in Cancer Prevention, Treatment, Recovery, and Survivorship
ONCOLOGY,  June 18, 2013
The Key to Reducing Quackery Lies in Healing Patients and Treating Their Experience
ONCOLOGY,  August 20, 2012
Quackery, Placebos, and Other Thoughts: An Integrative Oncologist’s Perspective
ONCOLOGY,  August 20, 2012
 
TOPIC INDEX

Cancer Types

 
  • Breast
  • Breast (HER2+)
  • Breast (Triple-Negative)
  • CML
  • Colorectal
  • Gastrointestinal
  • GIST
  • Genitourinary
  • Gynecologic
  • Head & Neck
  • Hematology
  • Kidney (Renal Cell)
  • Leukemia
  • Lung
  • Lymphoma
  • Melanoma
  • Multiple Myeloma
  • Ovarian
  • Prostate
  • Sarcoma

Supportive Care

More Topics

  • Bone Metastases
  • End-of-Life Care
  • Palliative Care
  • Ethics in Oncology
  • Practice Management
  • Practice & Policy


All Topics 


 
   SEARCH MEDICA RX
   Browse drugs by name:
A B C D E F G H I J
K L M N O P Q R S T
U V W X Y Z All      
   Search for drugs:
Search

 

 
FROM PHYSICIANS PRACTICE
Key Differences between FQHCs and RHCs
Chastity Werner, RHIT, June 13, 2013
FQHCs and RHCs take up a unique niche among physician practices. And that affects compensation and billing.
Improving Care Coordination in Your Practice
Susanne Madden,  June 12, 2013
Practices are feverishly working to control the rising costs of healthcare - effective care coordination can help.
Refunding Overpayments: Two Options for Medical Practices
Ericka L. Adler,  June 12, 2013
Medicare and Medicaid providers must return overpayments once identified. Here are two different refund approaches for practices to consider when necessary.
Four Easy Ways to Boost Patient Time of Service Collections
Aubrey Westgate,  June 12, 2013
Simple ways your medical practice staff can increase the likelihood patients will pay when presenting for appointments.
iPad Alternatives for Mobile Physicians
Marisa Torrieri, June 11, 2013
As more physicians are seeing the merits of media tablets, the market is expanding, too.
 

 

 
MOST POPULAR
  • Most Popular
  • Most Emailed
  • Most Recent
  • Papillary Thyroid Carcinoma
  • Robotic-Assisted Radical Prostatectomy: Who Is Benefiting?
  • ASCO: Long-Term Tamoxifen Benefit for Breast Cancer Confirmed
  • A 48-Year-Old Woman With Irregular Vaginal Bleeding
  • Dermatologic Adverse Events Associated With Targeted Therapies
  • Cannabis Linked to Decreased Bladder Cancer Risk
  • Breast Cancer Screening, Risk, and Options for High-Risk Women
  • Rising PSA Level in a 46-Year-Old Man
  • ASCO: Long-Term Tamoxifen Benefit for Breast Cancer Confirmed
  • Recurrent Epithelial Ovarian Cancer: An Update on Treatment
  • Soluble HER2 Levels Prognostic Factor in HER2+ Breast Cancer
  • ASCO: PD-L1 Antibody Elicits Durable Response in RCC
  • RECORD-3: Sunitinib Still Standard First-Line Treatment in Metastatic RCC
  • ASCO: Dabrafenib Shows Activity in BRAF-Mutated NSCLC Patients
  • Preventing Burnout in Oncology
Click here to subscribe to our newsletter
 
COMMENTS
  • Most Commented
  • Most Recent
  • 50 Shades of Pink—And Why It Helps to Know the Difference
  • Preventing Exposure to Hazardous Drugs
  • ASCO: Vinegar Screening Significantly Reduces Cervical Cancer Mortality
  • ASCO: Sulforaphane in Prostate Cancer Found Worthy of Further Investigation
  • Study: Recurrent Heartburn Ups Risk for Throat Cancer
  • Radiation-Induced Enteritis: Incidence, Mechanisms, and Management
  • HER2-Directed Therapy for Metastatic Breast Cancer
  • Accelerated Partial-Breast Irradiation: The Current State of Our Knowledge
  • It’s Time for Clinicians to Reconsider Their Proscription Against the Use of Soyfoods by Breast Cancer Patients
  • 50 Shades of Pink—And Why It Helps to Know the Difference
Click here to subscribe to our newsletter


 
SearchMedica Search Result

Find peer-reviewed literature and websites for practicing medical professionals

CME on Integrative Oncology
Evidence on Integrative Oncology
Guidelines on Integrative Oncology
Patient Education on Integrative Oncology
Clinical Trials on Integrative Oncology
Practical Articles on Integrative Oncology
Research and Reviews on Integrative Oncology
All "Integrative Oncology" results


CancerNetwork on Facebook

CancerNetwork | ConsultantLive | Diagnostic Imaging | Musculoskeletal Network | OBGYN.net | PediatricsConsultantLive |
Physicians Practice | Psychiatric Times | SearchMedica | Medical Resources

© 1996 - 2013 UBM Medica LLC, a UBM company
Privacy Statement - Terms of Service - Advertising Information - Editorial Policy Statement - UBM Medica Network Privacy Policy