Estrogen and Progesterone-related Gene Variants and Colorectal Cancer Risk

雌激素和孕激素相关基因变异与结直肠癌风险

基本信息

批准号：
7275969
负责人：
SHUMIN ZHANG
金额：
$ 30.48万
依托单位：
BRIGHAM AND WOMEN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2006
资助国家：
美国
起止时间：
2006-09-01 至 2010-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7275969
关键词：
10q24.3 11q22-q23 14q22 15q21.1 15q22 17q11-q21 22q11.21 2p21 5q21 6q25.1 Affect African American Alleles American Androgens Arts Asians Blood specimen Breast COMT gene CYP17A1 gene CYP19A1 gene CYP1A1 gene CYP1B1 gene Candidate Disease Gene Catabolism Catechol O-Methyltransferase Colorectal Colorectal Cancer Complex DNA Resequencing Data Development ESR1 gene ESR2 gene Environmental Exposure Enzymes Estrogen Receptors Estrogens Ethnic group European Exons Frequencies Future Genes Genetic Markers Genetic Polymorphism Genetic Variation Genotype HSD17B2 gene Haplotypes Hispanics Hysterectomy Intervention Introns Investigation Latino Length Malignant Neoplasms Malignant neoplasm of prostate Metabolism Methods Minor National Cancer Institute Numbers Observational Study Pacific Island Americans Personal Satisfaction Population Population Heterogeneity Postmenopause Progesterone Progesterone Receptors Progestin Therapy Progestins Randomized Controlled Clinical Trials Rate Research Personnel Resources Risk Role Sample Size Single Nucleotide Polymorphism Statistical Methods Structure Testing Untranslated Regions Variant Woman Women&apos s Health cancer risk carcinogenesis cohort design follow-up genotyping technology hormone therapy inhibitor/antagonist innovation novel prevent programs promoter prospective social

项目摘要

DESCRIPTION (provided by applicant): The Women's Health Initiative (WHI) trial has demonstrated that use of postmenopausal estrogen plus progestin therapy reduces risk of colorectal cancer in women, but use of estrogen alone among women with prior hysterectomy has no effect. These data suggest a complex effect of estrogen and progesterone on colorectal carcinogenesis. However, the underlying mechanisms by which estrogen and progesterone affect the development of colorectal cancer are poorly understood. Applying state-of-the-art genotyping technology and statistical methods, we will evaluate functional variants and determine the structure of haplotypes in 11 candidate genes important to estrogen and progesterone metabolism, and investigate their relationships with risk of colorectal cancer in the WHI observational study (OS) cohort, an ethnically diverse population. Specific studies will focus on genes encoding estrogen and progesterone receptors (ESR1, ESR2, and PGR) and enzymes responsible for local estrogen concentrations and the conversion of progesterone to estrogens via androgens (HSD17B1, HSD17B2, HSD17B4, CYP19A1, and CYP17A1) and for estrogen catabolism (CYP1A1, CYP1B1, and COMT). A total of 800 incident colorectal cancer cases and their two matched controls will be identified in the WHI-OS cohort of postmenopausal women with achieved blood samples and free of cancer at baseline. The WHI-OS cohort has a large number of confirmed cases of colorectal cancer and is well characterized with respect to use of postmenopausal hormone therapy and environmental exposures, thus providing an extraordinary opportunity to examine the main effects of gene variants and their interactions with use of combination hormone therapy vs. estrogen alone in relation to colorectal cancer risk. We also will explore interactions among these candidate genes. Hypotheses proposed in this application are novel, as the relations between estrogen and progesterone-related gene variants and risk of colorectal cancer are largely unexplored. Findings from this proposed study will help elucidate the roles of estrogen and progesterone in colorectal carcinogenesis, the differences between the effects of postmenopausal estrogen plus progestin therapy vs. estrogen alone on colorectal cancer risk observed in the WHI trial, and may suggest future targets for interventions to prevent colorectal cancer. Several unique features of the WHI-OS cohort, including its prospective design, diverse ethnic and social composition, large sample size, long duration, high follow-up rates, availability of stored blood specimens, and comprehensive covariate information, make this cohort a valuable and exceptional resource for the etiologic investigation of colorectal cancer.

描述（由申请人提供）：妇女健康倡议 (WHI) 试验表明，使用绝经后雌激素加孕激素治疗可降低女性患结直肠癌的风险，但对既往子宫切除术的女性单独使用雌激素则没有效果。这些数据表明雌激素和孕激素对结直肠癌的发生具有复杂的影响。然而，人们对雌激素和孕激素影响结直肠癌发展的潜在机制知之甚少。应用最先进的基因分型技术和统计方法，我们将在WHI观察性研究中评估功能变异并确定对雌激素和孕激素代谢重要的11个候选基因的单倍型结构，并研究它们与结直肠癌风险的关系（OS）队列，一个种族多样化的人群。具体研究将集中于编码雌激素和孕激素受体（ESR1、ESR2和PGR）的基因以及负责局部雌激素浓度和孕激素通过雄激素（HSD17B1、HSD17B2、HSD17B4、CYP19A1和CYP17A1）转化为雌激素的酶以及雌激素分解代谢（CYP1A1， CYP1B1 和 COMT）。 WHI-OS 绝经后妇女队列中将确定总共 800 例结直肠癌病例及其两个匹配的对照，这些妇女已获得血液样本且基线时没有癌症。 WHI-OS 队列有大量结直肠癌确诊病例，并且在绝经后激素治疗的使用和环境暴露方面具有良好的特征，因此提供了一个绝佳的机会来检查基因变异的主要影响及其与使用联合激素疗法与单独雌激素疗法与结直肠癌风险的关系。我们还将探索这些候选基因之间的相互作用。本申请中提出的假设是新颖的，因为雌激素和孕激素相关基因变异与结直肠癌风险之间的关系在很大程度上尚未被探索。这项拟议研究的结果将有助于阐明雌激素和孕激素在结直肠癌发生中的作用，以及 WHI 试验中观察到的绝经后雌激素加孕激素治疗与单独雌激素治疗对结直肠癌风险的影响之间的差异，并可能提出未来的干预目标以预防结直肠癌。 WHI-OS 队列的几个独特特征，包括其前瞻性设计、多样化的种族和社会构成、大样本量、持续时间长、高随访率、存储的血液样本的可用性以及全面的协变量信息，使该队列成为有价值的以及结直肠癌病因学研究的特殊资源。