Bone metabolism and bone metastases in prostate cancer

前列腺癌的骨代谢和骨转移

• 批准号: 8692714
• 负责人: Kathryn M. Wilson
• 金额: $ 31.6万
• 依托单位: HARVARD SCHOOL OF PUBLIC HEALTH
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-01 至 2018-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8692714
• 关键词: Address; Adult; Affect; Apoptosis; Biological Markers; Biological Process; Blood; Blood specimen; Bone Marrow; Bone Metastases Prevention; Bone Pain; Bone Tissue; Bone neoplasms; Calcium; Cancer Patient; Cell Proliferation; Characteristics; Clinical; Data; Development; Diagnosis; Diagnostic; Diet; Dietary Factors; Disease Progression; Disseminated Malignant Neoplasm; Ecosystem; Environment; Foundations; Fracture; Future; Gene Expression; Genes; Genome; Gleason Grade for Prostate Cancer; Goals; Growth; Health; Health Professional; Home environment; Hormones; Hypercalcemia; Life Style; Light; Link; Localized Malignant Neoplasm; Malignant Neoplasms; Malignant neoplasm of prostate; Measures; Mediating; Metastatic Neoplasm to the Bone; Metastatic Prostate Cancer; Neoplasm Metastasis; Obesity; Osteogenesis; Parathyroid Hormones; Pathway interactions; Patients; Phenotype; Phosphorus; Physicians; Plasma; Prevention; Prevention approach; Primary Neoplasm; Primary Prevention; Prostate; Prostatic Neoplasms; Public Health; Questionnaires; Risk; Risk Factors; Secondary Prevention; Seeds; Site; Soil; Specimen; Staging; Testing; Time; Tumor Biology; Tumor Markers; Tumor Tissue; Vitamin D; Vitamin K; Western World; angiogenesis; biobank; bone; bone health; bone metabolism; bone turnover; cancer diagnosis; case control; cohort; design; experience; fibroblast growth factor 23; follow-up; high risk; improved; lifestyle factors; mRNA Expression; men; mortality; neoplastic cell; novel strategies; osteogenic; prevent; prostate cancer cell; public health relevance; skeletal; spinal cord compression; tumor; tumor progression

DESCRIPTION (provided by applicant): Bone is the most common site of prostate cancer metastases, and prostate cancer with bone metastases is incurable. We propose to study which aspects of the tumor cells and the bone environment affect the development of bone metastasis in prostate cancer, which will improve risk prediction for patients and create new opportunities for preventing disease progression. We will also relate dietary factors and obesity to these tumor and bone characteristics to identify opportunities for primary and secondary prevention. We will leverage a unique cohort of men in the Health Professionals Follow-up Study and Physicians' Health Study for whom a biorepository of prostate tumor specimens and long-term follow-up data already exist. In addition, we will link this tumor tissue data to stored blood samples and questionnaire data on diet and lifestyle in the Health Professionals Follow-up Study. We hypothesize that primary tumor expression of bone-related genes may promote bone metastasis by facilitating prostate cancer cells' ability to home to, survive, and grow in bone tissue. We plan to use already collected whole genome mRNA expression data to study how bone-related gene expression relates to survival, and whether it adds predictive information beyond stage and Gleason grade. In addition, we hypothesize that men who have higher levels of bone turnover, or the on-going rebuilding of bone that all adults experience, are at higher risk for bone metastases because their bone environment facilitates the growth of disseminated tumor cells. We will study this hypothesis by measuring levels of several bone-regulating hormones and markers of bone turnover in men from blood samples collected prior to their cancer diagnosis, and relating these blood markers to prostate cancer survival. We will also assess how these blood markers of bone metabolism might have affected primary tumor cell expression of bone-related genes. Finally, we hypothesize that some risk factors for advanced prostate cancer, including obesity and dietary factors like calcium, vitamin D, phosphorus, and vitamin K, may impact prostate cancer progression through their effects on tumor expression of bone-related genes and on bone turnover and the skeletal environment. Rich dietary and lifestyle data available in the Health Professionals Follow-up Study allow us to link information on diet and obesity prior to prostate cancer diagnosis with tumor characteristics and circulating bone metabolism markers. Traditionally, risk factors for prostate cancer have been viewed in light of their direct effects on the prostate. We believe that studying them in light of their effets on tumor-bone interaction might elucidate the underlying mechanisms and improve opportunities for prevention of bone metastases in prostate cancer. Overall, this study will provide a wealth of information on tumor and bone characteristics that promote prostate cancer progression, providing improved risk prediction for patients and providing new approaches to the prevention and treatment of bone metastatic prostate cancer.

描述（申请人提供）：骨是前列腺癌最常见的转移部位，骨转移的前列腺癌是无法治愈的。我们建议研究肿瘤细胞和骨环境的哪些方面影响前列腺癌骨转移的发展，这将提高患者的风险预测，并为预防疾病进展创造新的机会。我们还将把饮食因素和肥胖与这些肿瘤和骨骼特征联系起来，以确定一级和二级预防的机会。我们将在健康专业人员随访研究和医生健康研究中利用一组独特的男性，他们的前列腺肿瘤标本和长期随访数据的生物库已经存在。此外，我们将把这些肿瘤组织数据与储存的血液样本和健康专业人员随访研究中的饮食和生活方式问卷数据联系起来。我们假设骨相关基因的原发肿瘤表达可能通过促进前列腺癌细胞在骨组织中定居、存活和生长的能力来促进骨转移。我们计划使用已经收集的全基因组mRNA表达数据来研究骨相关基因表达与生存的关系，以及它是否增加了分期和Gleason分级以外的预测信息。此外，我们假设那些有较高水平的骨更替，或者所有成年人都经历过的持续的骨重建的男性，风险更高