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TSPO Ligands for Cancer Imaging

用于癌症成像的 TSPO 配体

基本信息

批准号：
8881115
负责人：
Henry Charles Manning
金额：
$ 27.39万
依托单位：
VANDERBILT UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-09-01 至 2016-04-29
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8881115
关键词：
Affinity Apoptosis Aryl Hydrocarbon Receptor Binding Binding Proteins Biochemical Boxing Brain Brain Neoplasms Breast Cancer Biology Cholesterol Cholesterol Homeostasis Clinic Clinical Colorectal Complement Data Detection Development Diagnosis Drug Kinetics Exhibits Fluorine Future Glioma Goals Human Image Isoquinolines Isotopes Label Laboratories Lead Libraries Ligands Link Magnetic Resonance Imaging Malignant Neoplasms Malignant neoplasm of brain Manuscripts Methods Microfluidics Mitogen-Activated Protein Kinases Modeling Molecular Neoplasm Metastasis Outcome Pathway interactions Patients Pharmaceutical Chemistry Pharmaceutical Preparations Positron Positron-Emission Tomography Property Protein Binding Proteins Reporting Research Signal Transduction Specificity Specimen Steroid biosynthesis Techniques Testing Therapeutic Intervention Tissues Tracer Underserved Population base cancer imaging imaging agent imaging biomarker imaging probe improved in vitro Assay in vivo innovation molecular imaging monomer multidisciplinary neoplastic cell novel oncology outcome forecast pre-clinical preclinical study protein expression quantitative imaging radiochemical response screening small molecule targeted imaging tumor tumor growth tumor specificity uptake

项目摘要

DESCRIPTION (provided by applicant): This multidisciplinary proposal seeks to develop and validate a novel class of cancer imaging biomarkers for rapid clinical deployment. Leveraging advances in basic and clinical cancer biology, innovative medicinal chemistry, and high-throughput, small molecule screening, our laboratory has identified tumor-selective translocator protein (TSPO) ligands that are promising candidates for further development as positron emission tomography (PET) imaging agents. TSPO is an 18 kDa high-affinity cholesterol- and drug-binding protein that participates in cholesterol metabolism, steroid biosynthesis, proliferation, and apoptosis. Elevated levels of TSPO are well-documented in oncology, where levels correlate with tumor proliferation, invasion, and metastasis. Furthermore, our laboratory has mechanistically linked TSPO ligand binding to mitogen-activated protein kinase (MAPK) signaling in glioma. Capitalizing upon this observation, we have shown that TSPO ligand PET can be used to evaluate MAPK pathway inhibition in this setting. Collectively, these data demonstrate the potential significance of TSPO ligand PET as a predictive imaging biomarker in oncology. The overall goal of this study is to develop clinically translatable, tumor-selective TSPO imaging ligands that facilitate improved detection, molecular characterization, and prognosis of human gliomas. Our Specific Aims are [1] to optimize novel, tumor-selective TSPO ligand leads for in vivo PET imaging, [2] to develop methods for labeling promising TSPO ligands with the positron-emitting isotope fluorine-18, and [3] to evaluate promising TSPO imaging ligands in vivo.

描述（由申请人提供）：该多学科提案旨在开发和验证一类新型癌症成像生物标志物，用于快速临床部署。利用基础和临床癌症生物学，创新药物化学和高通量小分子筛选的进展，我们的实验室已经确定了肿瘤选择性转运蛋白（TSPO）配体，这些配体是进一步发展为正电子发射断层扫描（PET）成像剂的有前途的候选者。TSPO是一种18 kDa的高亲和力胆固醇和药物结合蛋白，参与胆固醇代谢、类固醇生物合成、增殖和凋亡。TSPO水平升高在肿瘤学中有充分的记录，其中水平与肿瘤增殖、侵袭和转移相关。此外，我们的实验室已经在神经胶质瘤中将TSPO配体结合与丝裂原活化蛋白激酶（MAPK）信号传导机制联系起来。利用这一观察结果，我们已经表明，TSPO配体PET可用于评估MAPK途径抑制在这种情况下。总的来说，这些数据证明了TSPO配体PET作为肿瘤学中的预测性成像生物标志物的潜在意义。本研究的总体目标是开发临床上可翻译的、肿瘤选择性的TSPO成像配体，以促进改善人类胶质瘤的检测、分子表征和预后。我们的具体目标是[1]优化用于体内PET成像的新型肿瘤选择性TSPO配体引线，[2]开发用正电子发射同位素氟-18标记有前景的TSPO配体的方法，以及[3]评估有前景的TSPO体内成像配体。