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Chemoprevention of Head & Neck Cancer Using Controlled Release Polymers

头部化学预防

基本信息

批准号：
8004085
负责人：
Susan R Mallery
金额：
$ 30.41万
依托单位：
OHIO STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-01-01 至 2013-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8004085
关键词：
1-Phosphatidylinositol 3-Kinase Acetylcysteine Address Adjuvant Affect American Angiogenesis Inhibitors Anti-Inflammatory Agents Anti-inflammatory Antioxidants Apoptosis Appearance Basement membrane Binding Cells Chemoprevention Chemopreventive Agent Cicatrix Clinical Clinical Trials Collagen Type XVIII Combined Modality Therapy Connective Tissue Critical Pathways Cytoprotection Data Development Diagnosis Dose Drug Delivery Systems Drug Kinetics Encapsulated Endostatins Epithelial Epithelial Cells Epithelium Ethanol Excision Freeze Drying Gel Gelatinase B Gelatinases Gene Expression Genes Glutathione Goals Growth Head and Neck Cancer Head and Neck Squamous Cell Carcinoma Health Human Immunotherapy Implant Individual Induction of Apoptosis Injectable Integrins Intervention Laboratories Left Location Malignant Epithelial Cell Malignant Neoplasms Malignant neoplasm of brain Malignant neoplasm of prostate Matrix Metalloproteinases Mediating Methods Microfilaments Molecular Morbidity - disease rate Nitric Oxide Synthase Nude Mice Operative Surgical Procedures Outcome Oxidation-Reduction Oxidative Stress PTGS2 gene Parents Pathway interactions Patient Noncompliance Patients Persons Pharmaceutical Preparations Phenotype Phosphotransferases Polymers Premalignant Prodrugs Property Prostate Protein S Radiation Radiation therapy Raspberries Reactive Nitrogen Species Recurrence Regimen Research Signal Transduction Site Source Staging Stromal Neoplasm Sulfhydryl Compounds Surface Surgical complication System Therapeutic Therapeutic Agents Tissues Transglutaminases Treatment Efficacy Treatment Failure Trocars Tumor Tissue Tumorigenicity Vascular Endothelial Growth Factors Vascular blood supply Water Wound Healing Xenograft procedure aggressive therapy angiogenesis base biodegradable polymer cancer recurrence caspase-3 cell motility chemotherapy cohort compliance behavior controlled release cytokine design effective therapy gene therapy human NOS2A protein implantation improved in vivo local drug delivery migration mortality nitrosative stress oral lesion poly(lactide)prevent proMMP-2 public health relevance synergism therapy development treatment site tumor tumor xenograft tumorigenesis tumorigenic

项目摘要

DESCRIPTION (provided by applicant): Over 50% of head and neck squamous cell carcinomas (HNSCC) recur despite multimodal therapy. As local treatment failures drive HNSCC morbidity and mortality, identification of effective treatments to prevent local recurrence has the potential to dramatically improve patient survival. One intervention strategy, which has proven effective in the management of both prostate and brain cancers, is the use of biodegradable polymer implants. While polymer implants provide a pharmacologic advantage, therapeutic benefits are highly dependent upon efficacy and possible synergism of the encapsulated agents. We propose to evaluate three derivatives of natural compounds: N-acetylcysteine (NAC), endostatin and a water-ethanol extract of freeze dried black raspberries, RO-ET. Studies in our laboratories have characterized some of the mechanisms by which NAC, endostatin and RO-ET suppress the HNSCC tumorigenic phenotype. NAC serves as a surrogate propeptide and inhibits activation and function of the basement membrane degrading gelatinase, MMP-9. Our data also show that the established angiostatic agent endostatin binds to HNSCC tropomysin microfilaments and inhibits HNSCC migration and invasion. RO-ET elicited a variety of chemopreventive effects in HNSCC cells that included reduction in VEGF release, inhibition of nitric oxide synthase, initiation of apoptosis and induction of differentiation. We hypothesize that the selected agents will reduce intracellular levels of reactive species, inhibit redox mediated gene expression and suppress pathways critical for HNSCC tumorigenesis. The research aims of this application are to: 1) determine effective agent dosing levels and evaluate agent combinations for synergistic or possible antagonistic effects (Aim 1.a.), 2) evaluate the effects of the chemopreventive agents on tumor-stromal interactions in HNSCC tumor explants (Aim 1.b.), 3) conduct pharmacokinetic analyses and determine therapeutic abilities to suppress HNSCC xenograft tumorigenesis (Aim 2) PUBLIC HEALTH RELEVANCE: head and neck cancer is a significant worldwide health problem, and a major reason for treatment failure is cancer recurrence. The goal of these studies is to identify effective cancer-preventing compounds for placement in controlled release delivery vehicles for implantation at the surgery site to prevent local treatment failures and inhibit development of new cancers.

描述（由申请人提供）：超过50%的头颈部鳞状细胞癌（HNSCC）复发，尽管多模式治疗。由于局部治疗失败导致HNSCC发病率和死亡率，因此确定有效的治疗方法以预防局部复发有可能显着提高患者的生存率。一种已被证明对前列腺癌和脑癌有效的干预策略是使用可生物降解的聚合物植入物。虽然聚合物植入物提供了药理学优势，但治疗益处高度依赖于包封剂的功效和可能的协同作用。我们建议评估三种天然化合物的衍生物：N-乙酰半胱氨酸（NAC），内皮抑素和冻干黑树莓的水-乙醇提取物，RO-ET。我们实验室的研究已经表征了NAC、内皮抑素和RO-ET抑制HNSCC致瘤表型的一些机制。NAC作为替代前肽，抑制基底膜降解明胶酶MMP-9的活化和功能。我们的数据还表明，建立血管抑制剂内皮抑素结合HNSCC原溶素微丝，抑制HNSCC迁移和侵袭。RO-ET在HNSCC细胞中引起多种化学预防作用，包括减少VEGF释放、抑制一氧化氮合酶、启动凋亡和诱导分化。我们假设所选择的药物将降低细胞内活性物质的水平，抑制氧化还原介导的基因表达，并抑制HNSCC肿瘤发生的关键途径。本申请的研究目的是：1）确定有效的药剂剂量水平并评价药剂组合的协同或可能的拮抗作用（目的1.a.），2)评价化学预防剂对HNSCC肿瘤外植体中肿瘤-基质相互作用的影响（目的1.b.），3)进行药代动力学分析并确定抑制HNSCC异种移植肿瘤发生的治疗能力（目标2）公共卫生相关性：头颈癌是一个重要的全球性健康问题，治疗失败的主要原因是癌症复发。这些研究的目的是确定有效的癌症预防化合物，用于放置在控释递送载体中，用于植入手术部位，以防止局部治疗失败并抑制新癌症的发展。