PTH-RELATED PEPTIDE AND VIT D IN PROSTATE CANCER GROWTH

PTH 相关肽和维生素 D 在前列腺癌生长中的作用

• 批准号: 6626721
• 负责人: MIRIAM FALZON
• 金额: $ 22.77万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-01-07 至 2005-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6626721
• 关键词: 1,25 dihydroxycholecalciferol; antisense nucleic acid; cell growth regulation; cell line; chemoprevention; gel mobility shift assay; genetic promoter element; hypercalcemia; neoplasm /cancer chemotherapy; neoplastic cell; parathyroid hormone related protein; prostate neoplasms; retinoate; transcription factor; transfection; transforming growth factors; vitamin D; vitamin analog

Prostate cancer is the largest cause of cancer death among men in the United States. Prostate cancer cells produce a variety of autocrine growth factors, among them the parathyroid hormone- related peptide (PTHrP). The first aim of this project will use two approaches to examine the effects of PTHrP on prostate cell growth: establishing cell lines over- or under-expressing PTHrP, and treating cells with recombinant PTHrP (1-139). Thus we can distinguish between the autocrine/paracrine (cell surface) vs. intracrine (nuclear) effects of the peptide. Vitamin D decreases prostate cancer cell growth and epidemiological studies have shown that vitamin D deficiency is a risk factor for prostate cancer. The long-term objective of our research is to determine whether vitamin D or its analogues are useful as chemopreventative or chemotherapeutic agents in prostate cancer. The PTHrP gene is down-regulated by 1,25-dihydroxyvitamin D (1,25(OH)2D), the hormonally active form of vitamin D, in prostate cancer cells. Therefore, vitamin D not only has antiproliferative effects, but decreases PTHrP secretion in prostate cells. This project seeks to define the mechanism(s) by which 1,25(OH)2D, alone and in combination with 9-cis-retinoic acid, represses PTHrP gene expression in normal and cancerous prostate cell lines. The human PTHrP gene is a complex transcriptional unit with at least three different promoters. Different cell lines and tissues exhibit different promoter utilization patterns. The responsiveness of each promoter to 1,25(OH)2D will be assessed using transient transfection assays. The precise sequence elements conferring responsiveness to 1,25(OH)2D within a particular promoter will be located by deletion mapping. Trans-acting nuclear proteins interacting with these promoter elements will be characterized by gel retardation and nuclease protection assays. The hypercalcemic effects of 1,25(OH)2D itself have thus far prevented its prophylactic and therapeutic use, but various non-hypercalcemic vitamin D analogues have recently been synthesized. Some of these analogues will be tested for their ability to down-regulate PTHrP gene expression and decrease PTHrP secretion, thereby addressing whether these derivatives exert the same net desirable effects as the parent compound. These studies should thus provide a molecular basis for use of non-hypercalcemic vitamin D analogues as chemopreventive and chemotherapeutic agents targeted at both PTHrP-mediated prostate cancer cell proliferation and humoral hypercalcemia of malignancy.

前列腺癌是美国男性癌症死亡的最大原因。前列腺癌细胞产生多种自分泌生长因子，甲状旁腺激素相关肽(PTHrP)就是其中之一。该项目的第一个目标将使用两种方法来检测PTHrP对前列腺细胞生长的影响：建立高表达或低表达PTHrP的细胞系，以及用重组PTHrP(1-139)处理细胞。因此，我们可以区分多肽的自分泌/旁分泌(细胞表面)和内分泌(核)效应。维生素D会减少前列腺癌细胞的生长，流行病学研究表明，维生素D缺乏是前列腺癌的危险因素。我们研究的长期目标是确定维生素D或其类似物作为前列腺癌的化学预防或化疗药物是否有用。在前列腺癌细胞中，PTHrP基因被1，25-二羟基维生素D(1，25(OH)2D)下调，1，25(OH)2D是维生素D的激素活性形式。因此，维生素D不仅具有抗增殖作用，而且还能减少前列腺细胞中PTHrP的分泌。本项目旨在确定1，25(OH)2D单独以及与9-顺式维甲酸联合抑制正常和癌症前列腺细胞系PTHrP基因表达的机制(S)。人类PTHrP基因是一个复杂的转录单位，至少有三个不同的启动子。不同的细胞系和组织表现出不同的启动子利用模式。每个启动子对1，25(OH)2D的响应性将通过瞬时转染试验来评估。将通过缺失作图定位特定启动子内对1，25(OH)2D具有响应性的精确序列元件。与这些启动子元件相互作用的反式核蛋白将通过凝胶滞留和核酸酶保护实验来鉴定。到目前为止，1，25(OH)2D本身的高钙作用阻碍了其预防和治疗用途，但最近合成了各种非高钙维生素D类似物。其中一些类似物将被测试其下调PTHrP基因表达和减少PTHrP分泌的能力，从而解决这些衍生物是否起到与母体化合物相同的净预期效果。因此，这些研究应该为使用非高钙维生素D类似物作为针对PTHrP介导的前列腺癌细胞增殖和恶性体液高钙血症的化学预防和化疗药物提供分子基础。