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Cholecalciferol (vitamin D3) in the prevention and treatment of prostate cancer: Effects and mechanisms of action.

机译:胆钙化固醇(维生素D3)在预防和治疗前列腺癌中的作用和作用机理。

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摘要

The objectives of this study were to examine: (i) the potential of cholecalciferol (vitamin D3) as an agent for treatment by inhibiting or reversing malignant characteristics of prostate cancer cells; (ii) its ability as a chemoprevention agent by reversing cellular changes associated with malignant transformation, and (iii) its mechanisms of action. Because cholecalciferol can inhibit cellular changes associated with malignant transformation and invasion, I propose that cholecalciferol may be an effective agent for treatment, and for secondary and tertiary prevention of prostate cancer.; Chemoprevention is the ultimate answer to reducing the high incidence of prostate cancer. The ability of cholecalciferol, to block or reverse changes associated with malignant transformation, was examined. Since immortalization is an early step in carcinogenesis, the immortalized but non-tumorigenic RWPE-1 human prostate epithelial cell line was used. RWPE-1 cells do not grow in agar and are not invasive. Physiological levels of cholecalciferol: (i) inhibited anchorage-dependent growth; (ii) decreased MMP-9 and MMP-2 activity; (iii) induced differentiation by decreasing vimentin but increasing PSA expression, and (iv) up-regulated VDR, RXRs, and AR, suggesting that its effects, in part, are receptor-mediated. Based on these in vitro studies, cholecalciferol appears to be an effective chemopreventive agent. I further show that RWPE-1 cells also express CPYP27A1, and its expression is up-regulated by cholecalciferol. Since the presence of 1alpha-hydroxylase has previously been shown, my results demonstrate that human prostate epithelial cells, target cells for vitamin D, have the necessary enzymes and the rare ability to locally produce the biologically active calcitriol from cholecalciferol. The mechanisms of action of cholecalciferol appear to involve the up-regulation of nuclear receptors and CYP27A1. Taken together, my results show that cholecalciferol may be an effective agent for chemoprevention and treatment of prostate cancer. (Abstract shortened by UMI.)
机译:这项研究的目的是检查:(i)胆钙化固醇(维生素D3)作为通过抑制或逆转前列腺癌细胞的恶性特征治疗的潜力; (ii)通过逆转与恶性转化相关的细胞变化,作为化学预防剂的能力,以及(iii)其作用机理。因为胆钙化固醇可以抑制与恶性转化和侵袭有关的细胞变化,所以我建议胆钙化固醇可能是治疗前列腺癌的有效手段,并且可以作为第二级和第三级预防。化学预防是减少前列腺癌高发的最终答案。检查了胆钙化固醇阻滞或逆转与恶性转化有关的变化的能力。由于永生化是癌发生的早期步骤,因此使用了永生化但非致瘤性的RWPE-1人前列腺上皮细胞系。 RWPE-1细胞不会在琼脂中生长,也不具有侵入性。胆钙化固醇的生理水平:(i)抑制锚定依赖性生长; (ii)MMP-9和MMP-2活性降低; (iii)通过降低波形蛋白而增加PSA表达来诱导分化,以及(iv)VDR,RXR和AR上调,表明其作用部分是受受体介导的。基于这些体外研究,胆钙化固醇似乎是一种有效的化学预防剂。我进一步表明RWPE-1细胞也表达CPYP27A1,其表达被胆钙化固醇上调。由于先前已经显示了1α-羟化酶的存在,因此我的结果表明,人前列腺上皮细胞(维生素D的靶细胞)具有必需的酶,并且难于从胆钙化固醇局部产生生物活性钙三醇。胆钙化固醇的作用机制似乎涉及核受体和CYP27A1的上调。综上所述,我的结果表明,胆钙化固醇可能是化学预防和治疗前列腺癌的有效药物。 (摘要由UMI缩短。)

著录项

  • 作者

    Tokar, Erik J.;

  • 作者单位

    Michigan State University.;

  • 授予单位 Michigan State University.;
  • 学科 Biology Cell.; Health Sciences Nutrition.; Health Sciences Oncology.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 322 p.
  • 总页数 322
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;预防医学、卫生学;肿瘤学;
  • 关键词

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