Chemoprevention of Head & Neck Cancer Using Controlled Release Polymers

项目概要/摘要R 01 CA 129609 A2 超过50%的头颈部鳞状细胞癌（HNSCC）复发， 疗法由于局部治疗失败导致HNSCC发病率和死亡率， 预防局部复发的有效治疗有可能显著改善患者的 生存一项干预战略，已证明对管理这两种疾病都有效 前列腺癌和脑癌，是使用可生物降解的聚合物植入物。而聚合物 植入物提供药理学优势，治疗益处高度依赖于 有效性和可能的协同作用。我们建议评估三个 天然化合物的衍生物：N-乙酰半胱氨酸（NAC），内皮抑素和水-乙醇 冷冻干燥黑树莓提取物，RO-ET。我们实验室的研究表明 NAC、内皮抑素和RO-ET抑制HNSCC的一些机制 致瘤表型NAC用作替代前肽并抑制活化和 基底膜降解明胶酶MMP-9的功能。我们的数据还显示， 已建立的血管抑制剂内皮抑制素结合HNSCC原溶素微丝， 抑制HNSCC迁移和侵袭。RO-ET在小鼠体内具有多种化学预防作用， HNSCC细胞，包括VEGF释放的减少，一氧化氮合酶的抑制， 启动凋亡和诱导分化。我们假设被选中的代理人 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， 抑制HNSCC肿瘤发生关键途径。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协同作用， 可能的拮抗作用（目标1.a.），2)评价化学预防剂的效果 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（Aim 2）。公共卫生相关性：头颈癌是一个重大的全球性健康问题， 治疗失败的主要原因是癌症复发。这些研究的目的是 鉴定用于控释递送有效的癌症预防化合物 用于在手术部位植入的载体，以防止局部治疗失败并抑制 发展新的癌症。

Project Summary/Abstract R01 CA129609A2 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.