Functional, cellular, and molecular imaging and therapy monitoring using ultrasou

使用超声波进行功能、细胞和分子成像和治疗监测

• 批准号: 8550779
• 负责人: STANISLAV Y EMELIANOV
• 金额: $ 53.4万
• 依托单位: UNIVERSITY OF TEXAS AT AUSTIN
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-25 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8550779
• 关键词: 3-Dimensional; Algorithms; Animal Cancer Model; Animal Model; Animals; Antibodies; Biochemical Genetics; Biodistribution; Biological; Blood; Cancer Center; Cancerous; Cell Surface Receptors; Cell physiology; Clinical Oncology; Contrast Media; Development; Doctor of Medicine; Ensure; Epidermal Growth Factor Receptor; Figs - dietary; Functional Imaging; Genetically Engineered Mouse; Goals; Gold; Hemoglobin; Histology; Human; Image; Imagery; Imaging Device; Imaging Techniques; Integrins; Lesion; Longitudinal Studies; Malignant Neoplasms; Molecular; Molecular Target; Monitor; Morphology; Mus; Nanosphere; Optical Methods; Optics; Outcome; Pathology; Performance; Physiological; Process; Property; Research; Research Personnel; Resolution; Signal Transduction; Silicon Dioxide; Specificity; Structure; System; Testing; Texas; Therapeutic Effect; Tissues; Toxic effect; Translations; Tumor Angiogenesis; Tumor-Derived; Tyrosine Kinase Inhibitor; Ultrasonography; Universities; Work; Xenograft procedure; angiogenesis; anticancer research; austin; base; cellular imaging; computerized data processing; cytotoxicity; experience; human disease; image processing; improved; in vivo; lapatinib; longitudinal animal study; malignant breast neoplasm; molecular imaging; mouse model; nanoparticle; nanorod; nanosized; neovasculature; overexpression; photoacoustic imaging; pre-clinical; pre-clinical research; prevent; programs; response; small molecule; tool; tumor; tumor progression

DESCRIPTION (provided by applicant): Small animal models, particularly genetically engineered mice, are increasingly recognized as powerful discovery tools in cancer research. However, the potential of animal models has not yet fully been realized since they are often sacrificed to perform tissue analysis to determine the effects of therapy. Sacrificing prevents long-term, in vivo observation of natural or perturbed processes. Therefore, there is a need for a morphologic, functional, cellular/molecular, and quantitative imaging technique capable of visualizing biochemical, genetic, or pharmacological processes in vivo and longitudinally in small animals. The overall goal of our academic-industrial partnership is to enable the molecular and cellular sensitivity of ultrasound-guided photoacoustic (USPA) imaging, furthering its development and translation into the preclinical research arena for longitudinal animal studies. Our hypothesis is that a non-invasive USPA imaging system, capable of simultaneous anatomical, functional, cellular and molecular visualization of cancer in small animals, will significantly enhance the outcome of fundamental and preclinical cancer research. The central theme of our application is to develop contrast agents and signal/image processing algorithms for USPA imaging to enable quantitative imaging of tumor angiogenesis and functional, cellular/molecular properties of tissue in small animal models of breast cancer. In this project we will specifically demonstrate our approach by developing imaging contrast agents sensitive to human epidermal growth factor receptor 2 (HER2) and the 1v23 integrin. These agents will be used to detect the molecular composition of a tumor in vivo to monitor the effect of the therapeutic small molecule tyrosine kinase inhibitor lapatinib on breast cancer cellular function and angiogenesis in longitudinal studies.

描述（由申请人提供）：小动物模型，特别是基因工程小鼠，越来越多地被认为是癌症研究中强大的发现工具。然而，动物模型的潜力尚未完全实现，因为它们经常被牺牲以进行组织分析以确定治疗效果。牺牲阻止了对自然或扰动过程的长期体内观察。因此，需要一种能够在小动物体内和纵向可视化生物化学、遗传或药理学过程的形态学、功能、细胞/分子和定量成像技术。 我们的学术-工业合作伙伴关系的总体目标是实现超声引导光声（USPA）成像的分子和细胞灵敏度，进一步将其开发和转化为纵向动物研究的临床前研究竞技场。我们的假设是，一个非侵入性的USPA成像系统，能够同时解剖，功能，细胞和分子可视化的癌症在小动物，将显着提高基础和临床前癌症研究的结果。 我们申请的中心主题是开发用于USPA成像的造影剂和信号/图像处理算法，以实现乳腺癌小动物模型中肿瘤血管生成和组织的功能、细胞/分子特性的定量成像。在本项目中，我们将通过开发对人表皮生长因子受体2（HER 2）和1v 23整合素敏感的成像造影剂来具体展示我们的方法。这些药物将用于检测体内肿瘤的分子组成，以监测治疗性小分子酪氨酸激酶抑制剂拉帕替尼在纵向研究中对乳腺癌细胞功能和血管生成的影响。