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The role of innate immunity and angiogenesis in osteosarcoma growth and metastasis.

机译:先天免疫和血管生成在骨肉瘤生长和转移中的作用。

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摘要

Osteosarcoma is the most common primary bone tumor in dogs and humans. Novel therapeutics are required since a number of patients will succumb to metastatic disease. Currently, it is known that a neoplastic mass contains more than transformed cells, but requires the presence of immune cells to create a supportive environment, and endothelial cells to form blood vessels to deliver oxygen and nutrients. Not only do these cells play a role in primary tumor growth, but they create an atmosphere conducive to invasion and metastasis, the primary cause of death for osteosarcoma patients. Therefore, better understanding of how immune and endothelial cells support metastatic growth is crucial for better understanding osteosarcoama.Utilizing murine tumor models, we have been able to explore the observation that patients with post-surgical infections have increased time to metastasis and increased survival. We have determined that this effect is mediated by NK cells and monocytes, which inhibit tumor growth through restriction of angiogenesis. We have also investigated the role of an anti-inflammatory therapeutic, tepoxalin, which leads to tumor growth inhibition. These observations explain the paradox of inflammation, where the type and timing of inflammation may inhibit or promote an anti-tumor effect.Due to the importance of angiogenesis and metastasis in osteosarcoma, we sought to develop new models and techniques to assess these processes. Fine needle aspiration coupled with flow cytometry accurately measures angiogenesis in cutaneous tumors, thereby allowing for repeated assessment of angiogenesis in a minimally invasive manner. We have also developed a novel post-surgical model of luciferase transfected murine osteosarcoma that grows orthotopically and spontaneously metastasizes, allowing us to non-invasively investigate the development of metastases. These tools will allow for investigation into novel anti-angiogenic and anti-metastatic compounds.Novel prognostic markers are required to better determine the outcome of cancer patients. We have determined that monocyte and lymphocyte counts from a pretreatment complete blood count are prognostic for disease free interval in dogs with osteosarcoma. These data describe the interactions between immune infiltrate and metastasis. The combination of the studies presented herein provides evidence for the interactions between the immune system and angiogenesis in the process of metastasis.
机译:骨肉瘤是狗和人中最常见的原发性骨肿瘤。由于许多患者将屈服于转移性疾病,因此需要新颖的疗法。目前,已知肿瘤块包含的细胞数量多于转化细胞,但需要存在免疫细胞才能形成支持性环境,并需要内皮细胞才能形成血管以输送氧气和营养。这些细胞不仅在原发性肿瘤的生长中发挥作用,而且还创造了一种有利于骨肉瘤患者死亡的主要原因-侵袭和转移的氛围。因此,更好地了解免疫细胞和内皮细胞如何支持转移性生长对于更好地了解骨肉瘤至关重要。通过使用鼠类肿瘤模型,我们能够探索观察到,患有术后感染的患者增加了转移时间并提高了生存率。我们已经确定这种作用是由NK细胞和单核细胞介导的,它们通过限制血管生成来抑制肿瘤的生长。我们还研究了抗炎治疗药物替泊沙林的作用,这种作用可抑制肿瘤的生长。这些发现解释了炎症的悖论,即炎症的类型和时机可能抑制或促进抗肿瘤作用。由于血管生成和转移在骨肉瘤中的重要性,我们寻求开发新的模型和技术来评估这些过程。细针抽吸结合流式细胞术可准确测量皮肤肿瘤中的血管生成,从而以微创的方式重复评估血管生成。我们还开发了一种新型的荧光素酶转染的小鼠骨肉瘤术后模型,该模型可在原位和自发转移生长,从而使我们能够无创地研究转移的发生。这些工具可用于研究新型抗血管生成和抗转移化合物。需要新颖的预后标记物才能更好地确定癌症患者的预后。我们已经确定,来自预处理全血细胞计数的单核细胞和淋巴细胞计数对于骨肉瘤犬的无病间隔预后是预后的。这些数据描述了免疫浸润和转移之间的相互作用。本文介绍的研究相结合,为转移过程中免疫系统与血管生成之间的相互作用提供了证据。

著录项

  • 作者

    Sottnik, Joseph L.;

  • 作者单位

    Colorado State University.;

  • 授予单位 Colorado State University.;
  • 学科 Biology Cell.Health Sciences Oncology.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 288 p.
  • 总页数 288
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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