Green tea-mediated inhibition of aberrant DNA hypermethylation in prostate cancer

绿茶介导抑制前列腺癌异常 DNA 高甲基化

• 批准号: 7295730
• 负责人: ADAM R. KARPF
• 金额: $ 14.55万
• 依托单位: ROSWELL PARK CANCER INSTITUTE CORP
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-15 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7295730
• 关键词: Accounting; Animals; Biological Markers; Cancer Death Rates; Cancer Patient; Chemoprevention; Chemopreventive Agent; Clinical; Clinical Research; CpG Islands; DNA; DNA Methylation; DNA Methyltransferase; DNA Modification Methylases; Data; Diagnostic Neoplasm Staging; Dietary Intervention; Distant; Dose; Elderly; End Point; Epidemiologic Studies; Epigallocatechin Gallate; Epigenetic Process; Etiology; Gene Expression; Genes; Genomics; Glutathione S-Transferase; Green tea; Guanosine Triphosphate; Hypermethylation; Incidence; Infusion procedures; Investigation; Laboratories; Malignant neoplasm of prostate; Measurement; Mediating; Methionine; Methods; Methylation; Methyltransferase; Modeling; Molecular; Mus; Neoplasm Metastasis; Numbers; Oncogenic; Oral; Oral Administration; Pattern; Polymerase Chain Reaction; Prevention; Primary Neoplasm; Property; Prostate; Prostatic Intraepithelial Neoplasias; Research Personnel; Role; Scanning; Site; Staging; Testing; Time; Transferase Gene; Transgenic Organisms; Tumor Burden; Tumor stage; Water; Week; Western Blotting; adenoma; base; cohort; design; inhibitor/antagonist; mRNA Expression; men; mouse model; novel; prevent; programs; protein expression; research study; response; sodium bisulfite; tumor; tumor progression; tumorigenesis

DESCRIPTION (provided by applicant): A role for green tea in the prevention of human prostate cancer is supported by both epidemiological studies and laboratory investigations. Green tea extract (GTP) contains a number of bioactive polyphenolic compounds that account for its anti-carcinogenic properties. Previous studies have shown that oral infusion of GTP dramatically reduces tumor burden and metastasis in a spontaneous autochthonous transgenic mouse model of prostate cancer known as TRAMP. These data support the use of the TRAMP model to examine the molecular mechanisms involved in GTP-mediated prostate cancer chemoprevention. Recently, green tea polyphenols were identified as potent inhibitors of DNA methylation, a critical oncogenic mechanism. This suggests a novel and direct mechanism to account for the chemopreventive properties of GTP. Based on these data, it is hypothesized that DNA methylation changes are involved in the etiology of TRAMP prostate cancer, and that the chemopreventive effect of GTP in TRAMP is due to its ability to prevent or reverse aberrant DNA hypermethylation. To test this hypothesis, this proposal will: 1) Define the epigenetic changes coincident with prostate cancer progression in the TRAMP model; and 2) Determine the effect of GTP treatment on epigenetic parameters in TRAMP mice. Because prostate cancer has a long latency period and is most prevalent in men over the age of 65, dietary interventions that modestly delay progression time would have a profound impact on prostate cancer death rates. In this regard, GTP has the potential for significant utility as a chemopreventive agent in prostate cancer patients. Understanding the molecular mechanism(s) responsible for the activity of GTP is essential for the optimal design of prostate cancer chemoprevention trials and for the identification of novel molecular biomarkers to follow in clinical studies of GTP.

描述（由申请人提供）：

项目成果

Expression level and DNA methylation status of glutathione-S-transferase genes in normal murine prostate and TRAMP tumors.

• DOI: 10.1002/pros.20976
• 发表时间: 2009-09-01
• 期刊: PROSTATE
• 影响因子: 2.8
• 作者: Mavis, Cory K.;Kinney, Shannon R. Morey;Foster, Barbara A.;Karpf, Adam R.
• 通讯作者: Karpf, Adam R.

Lack of evidence for green tea polyphenols as DNA methylation inhibitors in murine prostate.

• DOI: 10.1158/1940-6207.capr-09-0010
• 发表时间: 2009-12
• 期刊: Cancer prevention research (Philadelphia, Pa.)
• 作者: Morey Kinney SR;Zhang W;Pascual M;Greally JM;Gillard BM;Karasik E;Foster BA;Karpf AR
• 通讯作者: Karpf AR