Prostate cancer and genes of the one-carbon cycle

前列腺癌和一碳循环基因

基本信息

批准号：
7650245
负责人：
CHARNITA M. ZEIGLER-JOHNSON
金额：
$ 13.87万
依托单位：
UNIVERSITY OF PENNSYLVANIA
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-07-01 至 2011-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7650245
关键词：
Affect African American American Award Biological Biological Markers Biological Process Cancer Burden Cancer Etiology Carbon Case-Control Studies Cessation of life Complex Cutaneous DNA DNA Methylation DNA Structure Data Diet Dietary Factors Disease Disease Outcome Disease Progression Elderly Environmental Exposure Environmental Risk Factor Epidemiologic Studies Ethnic Origin Etiology Family Folate Frequencies Funding Gene-Modified Genes Genetic Genetic Polymorphism Genotype Haplotypes Hospitals Incidence Individual Intake MTHFR gene Malignant Neoplasms Malignant neoplasm of prostate Measures Metabolism Methylation Nucleotides Nutritional Oncogenes Pathway interactions Pattern Population Heterogeneity Race Research Research Design Research Personnel Resources Risk Risk Factors Sample Size Severities Supplementation Variant Weight advanced disease analytical method base cancer risk case control design folic acid metabolism gene interaction high risk interest men methyl group molecular marker novel racial difference trait tumor

项目摘要

DESCRIPTION (provided by applicant): Prostate cancer is the most prevalent cancer and is the second major cause of cancer-related deaths among American men. However, little is known about the etiology of prostate cancer and the risk factors for advanced disease. Recently, dietary influences that may alter methylation patterns in DNA have been implicated in the etiology of various cancers. However, few investigators have examined the relationship between DNA methylation and genotypes that may be associated with prostate cancer. The objective of this proposal is to explore the potential relationship between prostate cancer and the major genes affecting DNA methylation through folate metabolism pathways. We hypothesize (1) that both biological and environmental factors influence prostate cancer onset in sporadic cases and (2) that ethnic/cultural differences in these factors may explain racial differences in patterns of disease. The overall aim of this study is to use novel analytical methods to determine whether common variants in select one- carbon metabolizing genes modify the risk of sporadic prostate cancer in a diverse population. The presence of an association may help to identify the course of disease progression and the individuals who are most likely to develop prostate cancer and progress the quickest. The effect of folate on prostate cancer occurrence is likely to involve interactions of genes at various loci and environmental exposures. Therefore, simultaneous consideration of multiple predictors in the context of a carefully designed epidemiologic study is important. The genes to be studied in this research include MTHFR, CBS, MS, MSRR, TS, and SHMT. Novel analytical methods, including CART, haplotype analysis, and trimming and weighting, will be explored. An ongoing currently funded hospital-based case-control study design will be used to accomplish the following three specific aims: (1) To determine the frequencies of genotypes associated with folate metabolism by race/ethnicity; (2) To determine the association between prostate cancer and genotypes associated with one-carbon metabolism; (3) To determine the effect of folate intake and genotype on prostate cancer occurrence and progression.

描述（由申请人提供）：前列腺癌是最常见的癌症，也是美国男性癌症相关死亡的第二大原因。然而，人们对前列腺癌的病因和晚期疾病的危险因素知之甚少。最近，可能改变 DNA 甲基化模式的饮食影响与各种癌症的病因学有关。然而，很少有研究人员研究过 DNA 甲基化和可能与前列腺癌相关的基因型之间的关系。该提案的目的是探索前列腺癌与通过叶酸代谢途径影响 DNA 甲基化的主要基因之间的潜在关系。我们假设（1）生物和环境因素都会影响散发病例中前列腺癌的发病；（2）这些因素中的种族/文化差异可能解释疾病模式的种族差异。本研究的总体目标是使用新颖的分析方法来确定选定的一碳代谢基因中的常见变异是否会改变不同人群中散发性前列腺癌的风险。关联的存在可能有助于确定疾病进展的过程以及最有可能患前列腺癌和进展最快的个体。叶酸对前列腺癌发生的影响可能涉及不同位点的基因相互作用和环境暴露。因此，在精心设计的流行病学研究中同时考虑多个预测因素非常重要。本研究要研究的基因包括MTHFR、CBS、MS、MSRR、TS和SHMT。将探索新的分析方法，包括 CART、单倍型分析以及修剪和加权。目前正在资助的基于医院的病例对照研究设计将用于实现以下三个具体目标：（1）按种族/民族确定与叶酸代谢相关的基因型频率； (2) 确定前列腺癌与一碳代谢相关基因型之间的关联； (3)确定叶酸摄入量和基因型对前列腺癌发生和进展的影响。