Sensitivity enhanced MRI imaging of receptor binding in breast cancer

乳腺癌受体结合的灵敏度增强 MRI 成像

基本信息

批准号：
9750746
负责人：
Nirbhay Narayan Yadav
金额：
$ 20.2万
依托单位：
HUGO W. MOSER RES INST KENNEDY KRIEGER
依托单位国家：
美国
项目类别：
财政年份：
2018
资助国家：
美国
起止时间：
2018-08-01 至 2021-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9750746
关键词：
Acids Affinity Anatomy Animals Asses Bathing Binding Breast Breast Cancer Cell Caffeine Cancer Patient Cause of Death Cell Line Cell surface Cells Chemicals Clinic Clinical Contrast Media Coupling Detection Development Diagnosis Discipline of Nuclear Medicine Drug Targeting Early Diagnosis Ensure Equipment Exhibits FDA approved Frequencies Funding Glucose Glutamates Glycogen Glycolysis Goals Human Image Imaging Techniques Immobilization In Vitro Industrialization Infusion procedures Isotopes Label Ligand Binding Ligands Magnetic Resonance Imaging Magnetism Malignant Neoplasms Mediating Metabolism Methods Modality Modification Molecular Molecular Probes Molecular Target Monitor Nature Neoplasm Metastasis Outcome Peptides Pharmaceutical Preparations Physiologic pulse Positron-Emission Tomography Proteins Protocols documentation Protons Relapse Resolution Scheme Serum Proteins Signal Transduction Solid Specificity Techniques Technology Translating Water base cancer subtypes cancer type cell type crosslink design experimental study glucosaminoglycans imaging approach imaging modality in vivo individual patient interest link protein malignant breast neoplasm molecular imaging molecular pump myoinositol non-invasive monitor novel outcome forecast personalized medicine pre-clinical radio frequency receptor receptor binding soft tissue solute targeted imaging targeted treatment theranostics therapeutic target tool treatment planning treatment response tumor tumor heterogeneity tumorigenesis

项目摘要

Cancer remains one of the leading causes of death in the industrialized world. In recent years, there has been a resurgence of interest in tumor lactate metabolism since lactate has been associated with metastases and poor prognosis in cancer patients. Recent discoveries have identified that the cell surface lactate receptor HCA1 is associated with tumorigenesis and metastasis and thus an attractive imaging target and possible therapeutic target. However, because lactate exhibits low affinity and a fast turnover rate, current in vivo molecular imaging techniques are not well suited to image these types of targets. We have developed a novel MRI based approach for detecting the low affinity binding of natural (no chemical modification) substrates to molecular targets and a unique molecular pump scheme that enhances the sensitivity two to three orders of magnitude thus making this technology applicable for in vivo studies. Importantly, this method can be implemented on standard MRI hardware and thus rapidly translated to the clinic. We propose developing, optimizing, and validating this approach for imaging the binding of lactate to HCA1 receptors in breast cancer. In AIM 1, we will validate the specificity of detecting lactate-HCA1 binding in vitro using (i) perfused breast cancer cells that express different levels of the HCA1 receptor, and (ii) MRI pulse sequence optimization. In AIM 2, we will validate the specific binding of lactate to breast cancer cells in vivo. We will further probe lactate binding using the infusion of L-lactate or D-glucose (metabolized to lactate), both FDA approved for iv use in humans. These aims are expected to result in a MRI method for imaging the binding of low-affinity ligands to a cell target. Due to the nature of the labelling approaches, these MRI methods will be highly tunable to a broad range of other substrates-target pairs.

癌症仍然是工业化世界中死亡的主要原因之一。近年来，由于乳酸与转移和转移有关癌症患者的预后不良。最近发现的发现细胞表面乳酸受体 HCA1与肿瘤发生和转移有关，因此是一个有吸引力的成像靶标的治疗靶标。但是，由于乳酸表现出低亲和力和快速的周转率，因此当前体内分子成像技术不太适合成像这些类型的目标。我们已经开发了一本小说基于MRI的方法，用于检测天然（无化学修饰）底物的低亲和力结合与分子靶标和独特的分子泵方案，可增强灵敏度2至三个顺序大小，因此该技术适用于体内研究。重要的是，此方法可以是根据标准MRI硬件实施，因此迅速转化为诊所。我们建议发展，优化并验证这种方法以对乳腺癌中乳酸与HCA1受体的结合进行成像。在AIM 1中，我们将验证使用（i）灌注在体外检测乳酸-HCA1结合的特异性表达不同水平HCA1受体的乳腺癌细胞和（ii）MRI脉冲序列优化。在AIM 2中，我们将验证乳酸在体内与乳腺癌细胞的特异性结合。我们将进一步探针乳酸结合使用L-乳酸或D-葡萄糖（代谢为乳酸），均为FDA 被批准用于人类使用。这些目标有望导致MRI方法成像低亲和力配体与单元目标。由于标签方法的性质，这些MRI方法将高度调节广泛的其他底物目标对。