Predictive model of pro- and anti-angiogenic factors involved in breast cancer

乳腺癌中促血管生成因子和抗血管生成因子的预测模型

• 批准号: 8305964
• 负责人: Stacey Deleria Finley
• 金额: $ 2.25万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-15 至 2013-02-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8305964
• 关键词: Accounting; Address; Angiogenesis Inducing Agents; Angiogenesis Inhibition; Angiogenesis Inhibitors; Angiogenic Factor; Angiogenic Peptides; Binding; Biological; Biological Process; Blood Platelets; Blood Vessels; Blood capillaries; CD36 gene; CD47 gene; Cancer Patient; Clinical; Clinical Data; Complex; Computer Simulation; Conflict (Psychology); Data; Development; Diagnosis; Disease; Elements; Endothelial Cells; Equilibrium; Event; Extracellular Matrix Proteins; Functional disorder; Growth; Growth Factor; Human; Hypoxia; Laboratories; Malignant Neoplasms; Measurement; Membrane; Modeling; Molecular; Neoplasm Metastasis; Pathway interactions; Peptides; Physiological; Physiology; Plasma; Process; Proteoglycan; Reporting; Research; Role; Simulate; Site; Source; Systems Biology; Testing; Therapeutic; Therapeutic Intervention; Thrombospondin 1; Time; Tissues; Tumor Angiogenesis; Tumor Pathology; Vascular Endothelial Growth Factors; Vascular blood supply; Vascularization; Woman; Work; angiogenesis; base; bevacizumab; cancer cell; cancer therapy; capillary; inhibitor/antagonist; insight; malignant breast neoplasm; new growth; predictive modeling; promoter; public health relevance; receptor; research study; response; simulation; tumor; tumor growth

DESCRIPTION (provided by applicant): Cancer development, invasion, and metastasis is largely dependent on angiogenesis, the formation of new capillaries from pre-existing blood vessels, and this process is exquisitely regulated by a balance of pro- and anti-angiogenic factors. Stimulators of angiogenesis include growth factors, such as vascular endothelial growth factor (VEGF), a key promoter of vascular growth. Additionally, membrane-bound or extracellular matrix proteins, including thrombospondin-1 (TSP1), function as endogenous inhibitors of angiogenesis. In the case of cancer, the balance is altered, leading to a state of hyper-vascularization and allowing the tumor to establish its own blood supply. A quantitative description of the dynamic equilibrium of promoters and inhibitors of vascular growth would aid in our understanding of tumor angiogenesis and provide a platform to test cancer therapies that control this process. The proposed research aims to develop an experiment-based computational model of breast cancer angiogenesis that incorporates endogenous pro- and anti-angiogenic pathways (Aim 1). The model will be used to probe the mechanism by which TSP1 inhibits vascular growth and quantify the role of platelets in angiogenesis (Aim 2). Additionally, the model will simulate and predict the angiogenic response to breast cancer therapies, including VEGF-neutralizing agents and TSP1-derived anti- angiogenic peptides (Aim 3). This research will further our understanding of angiogenesis-related pathophysiology and facilitate the development and optimization of cancer therapies that inhibit tumor angiogenesis. PUBLIC HEALTH RELEVANCE: More than 180,000 women are diagnosed with breast cancer each year. Cancer development, leading to invasion and metastasis, is largely governed by the cancer cells' ability to promote the growth of new blood vessels from pre-existing ones, a process called angiogenesis. This project aims to develop a quantitative model to study the balance of promoters and inhibitors of angiogenesis and apply the model to aid in the development of cancer therapeutics.

描述（由申请人提供）：癌症的发展，侵袭和转移在很大程度上取决于血管生成，从既有血管中的新毛细血管形成新毛细血管的形成，并且该过程受到促和抗血管生成因子的平衡的精致调节。血管生成的刺激剂包括生长因子，例如血管内皮生长因子（VEGF），这是血管生长的关键启动子。此外，膜结合或细胞外基质蛋白（包括血小板蛋白1（TSP1））起着血管生成的内源性抑制剂的作用。在癌症的情况下，平衡会改变，导致过度血管化状态，并允许肿瘤建立自己的血液供应。对启动子和血管生长抑制剂的动态平衡的定量描述将有助于我们理解肿瘤血管生成，并为控制该过程的癌症治疗提供了一个平台。拟议的研究旨在开发一种基于实验的乳腺癌血管生成的计算模型，该模型融合了内源性促促促血管生成和抗血管生成途径（AIM 1）。该模型将用于探测TSP1抑制血管生长并量化血小板在血管生成中的作用的机制（AIM 2）。此外，该模型将模拟和预测对乳腺癌疗法的血管生成反应，包括VEGF中和剂和TSP1衍生的抗血管生成肽（AIM 3）。这项研究将进一步了解与血管生成相关的病理生理学，并促进抑制肿瘤血管生成的癌症疗法的发展和优化。 公共卫生相关性：每年有18万名女性被诊断出患有乳腺癌。癌症的发展，导致侵袭和转移，在很大程度上受癌细胞促进新血管生长的能力，这是一种称为血管生成的过程。该项目旨在开发一个定量模型来研究启动子和血管生成抑制剂的平衡，并应用模型来帮助开发癌症治疗剂。