Role of p53 polymorphisms in disparities in breast carcinogenesis and outcome .

p53 多态性在乳腺癌发生和结果差异中的作用。

• 批准号: 8777010
• 负责人: ROBIN S FUCHS-YOUNG
• 金额: $ 36.5万
• 依托单位: TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-03-13 至 2016-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8777010
• 关键词: Address; African American; Alleles; Animal Model; Apoptosis; Apoptotic; Arginine; Biological; Body Weight; Breast; Breast Cancer Model; Breast Cancer Patient; Breast Carcinogenesis; Caucasians; Codon Nucleotides; Collaborations; Databases; Development; Disease; ERBB2 gene; Economic Factors; Environmental Risk Factor; Epidemiologic Studies; Epidemiology; Epithelium; Equilibrium; Exons; Frequencies; Genetic; Genetic Polymorphism; Genetic Predisposition to Disease; Genotype; Goals; Growth Factor; Health; Hormonal; Human; Human Genetics; In Vitro; Incidence; Indium; Individual; Insulin-Like Growth Factor I; Light; Malignant Neoplasms; Mammary Neoplasms; Mammary Tumorigenesis; Mammary gland; Mediator of activation protein; Melissa; Minority; Modeling; Molecular; Molecular Target; Multiparity; Mutation; Oncogenic; Outcome; Pathway interactions; Phenotype; Population; Positioning Attribute; Postmenopause; Predisposition; Pregnancy; Premenopause; Prevention strategy; Proline; Protein p53; Public Health; Risk; Risk Factors; Role; Sampling; TP53 gene; Testing; Tumor Bank; Variant; Woman; base; cancer health disparity; early onset; energy balance; genetic analysis; health disparity; homologous recombination; improved; in vitro Model; in vivo; inhibitor/antagonist; malignant breast neoplasm; mouse model; novel; outcome forecast; overexpression; parity; racial disparity; research study; response; social; treatment strategy; tumor; tumorigenesis

DESCRIPTION (provided by applicant): Minority women, specifically African Americans (AAs), are substantially more likely than Caucasians to develop early onset breast cancer (EOBC) that is frequently aggressive and has a poor prognosis. In addition, epidemiologic studies have shown that AA women do not enjoy the same protection conferred by early full- pregnancy and multiparity as do Caucasian women. Some of these studies show that the risks of pre- menopausal breast cancer and more aggressive forms of the disease are actually increased by parity and early pregnancy in AA women. The molecular basis for this racial disparity is not known, but it is likely that the highly proliferative state achieved during development of the lactational differentiation, without appropriate homeostatic balance produced by subsequent waves of apoptosis, could contribute to this increased risk. We hypothesize that racially disproportionate p53 variants with reduced or altered function contribute to breast cancer health disparities and lack of pregnancy protection in AA women. In particular we propose that a non-synonymous SNP that results in either a proline (P) or arginine (R) at position 72 of the p53 protein may be an important contributor to this health disparity. The frequency of the P allele, which has been shown to be a less potent inhibitor of oncogenic transformation in vitro and to have reduced capacity to induce apoptosis in vivo, is much higher (66.6%) in AA than in Caucasian women (23.3%). We will test this hypothesis using the one existing animal model that harbors a "humanized" p53 gene, obtained by targeted homologous recombination of exon 4, encoding either R or P at codon 72. In specific aim 1, we will use this animal model to investigate whether the P allele, which is more frequent in AA women, provides a reduced level of pregnancy- induced mammary cancer protection than the R allele, which is more prevalent in Caucasian women. In specific aim 2, using the same animal model, we will investigate if the P allele cooperates with HER-2 in development of aggressive, early onset disease. Overexpression of Her-2 is one of the most common genetic alterations found in tumors from young AA breast cancer patients. In specific aim 3, we will investigate if the p53 alleles interact with the IGF-1 pathway. IGF-1 is an important mediator of the effects of energy balance and is another putative target of molecular alteration during mammary tumorigenesis. Finally, in Aim 4 we will investigate whether our mechanistic findings in animal models can be substantiated in human samples obtained from AA breast cancer patients. It is anticipated that these novel studies will shed new light on the molecular basis for outcome disparities in breast cancer, particularly the interactions of biological risk factors that may contribute to development of aggressive, early onset disease. Since a better understanding of the mechanisms involved in breast carcinogenesis in minority populations carries the promise of improved prevention and treatment strategies, this project directly and innovatively addresses the goal of reducing and/or eliminating health disparities.

描述（由申请人提供）：少数民族妇女，特别是非洲裔美国人（AAs），比高加索人更有可能患上早发性乳腺癌（EOBC），这种癌症通常具有侵袭性，预后不良。此外，流行病学研究表明，AA妇女不享有同样的保护所赋予的早期充分怀孕和多胎作为高加索妇女。其中一些研究表明，绝经前乳腺癌和更积极的形式的疾病的风险实际上是增加了产次和早期怀孕的AA妇女。这种种族差异的分子基础尚不清楚，但很可能是在哺乳期分化发育过程中达到的高度增殖状态，没有随后的细胞凋亡波产生的适当的稳态平衡，可能导致这种风险增加。 我们假设，种族不成比例的p53变异减少或改变功能，有助于乳腺癌的健康差异和缺乏怀孕保护AA妇女。特别地，我们提出，在p53蛋白的位置72处导致脯氨酸（P）或精氨酸（R）的非同义SNP可能是这种健康差异的重要贡献者。P等位基因在AA中的频率（66.6%）远高于高加索女性（23.3%），P等位基因在体外被证明是一种较弱的致癌转化抑制剂，在体内诱导细胞凋亡的能力降低。我们将使用一种现有的动物模型来检验这一假设，该模型含有“人源化”p53基因，该基因是通过外显子4的靶向同源重组获得的，在密码子72处编码R或P。在具体目标1中，我们将使用该动物模型来研究在AA女性中更常见的P等位基因是否比在高加索女性中更普遍的R等位基因提供降低水平的妊娠诱导的乳腺癌保护。在具体目标2中，使用相同的动物模型，我们将研究P等位基因是否与HER-2合作发展侵袭性早发性疾病。Her-2的过表达是在年轻AA乳腺癌患者的肿瘤中发现的最常见的遗传改变之一。在具体目标3中，我们将研究p53等位基因是否与IGF-1通路相互作用。IGF-1是能量平衡效应的重要介质，并且是乳腺肿瘤发生过程中分子改变的另一个假定靶点。最后，在目标4中，我们将研究我们在动物模型中的机制发现是否可以在从AA乳腺癌患者获得的人类样本中得到证实。 预计这些新的研究将揭示乳腺癌结局差异的分子基础，特别是可能导致侵袭性早发性疾病发展的生物风险因素的相互作用。由于更好地了解少数群体中乳腺癌发生的机制，有希望改善预防和治疗战略，该项目直接和创新地解决了减少和/或消除健康差距的目标。