A mouse model of TGFbeta1 and tumor immunosurveillance in Squamous cell cancer

TGFbeta1 和鳞状细胞癌肿瘤免疫监视的小鼠模型

• 批准号: 7260505
• 负责人: ADAM b GLICK
• 金额: $ 21.46万
• 依托单位: PENNSYLVANIA STATE UNIVERSITY, THE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-15 至 2010-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7260505
• 关键词: A Mouse; Antibodies; Area; Benign; Binding; Biochemical; Cells; Chronic; Data; Development; Diagnostic Neoplasm Staging; Disease regression; Epidermis; Epithelial; Epithelial Cells; Gene Expression; General Population; Genetic; Goals; Human; Hyperplasia; Immune; Immune response; Immune system; Immunocompromised Host; Immunologic Monitoring; Immunosuppression; In Vitro; Incidence; Inflammation; Inflammatory; Lead; Link; Malignant Neoplasms; Malignant Squamous Cell; Malignant Squamous Cell Neoplasm; Methods; Molecular Analysis; NF-kappa B; Oncogenic; Organ Transplantation; Papilloma; Pathway interactions; Protein Overexpression; Public Health; Rag1 Mouse; Research Personnel; Research Project Grants; Research Proposals; Role; Signal Transduction; Site; Skin; Skin Cancer; Skin Carcinogenesis; Skin Carcinoma; Squamous cell carcinoma; Staging; Stimulus; TNFRSF5 gene; Testing; Transgenes; Transgenic Organisms; Transplant Recipients; Tumor Promotion; Tumor Suppressor Proteins; Tumor stage; Tumor-Derived; base; cancer therapy; cytokine; dimethylbenzanthracene; in vivo; keratinocyte; mouse model; neoplastic cell; programs; ras Oncogene; response; therapeutic target; tumor; tumor progression

DESCRIPTION (provided by applicant): TGFbeta1 has both tumor suppressor and oncogenic roles in human cancer development, but the mechanisms underlying this change in function remain elusive. Identifying the mechanisms underlying these distinct functions of TGFbeta1 and how this change occurs will provide important new targets for cancer therapy. We have recently developed a TGFbeta1 conditional epidermal expression mouse model to identify tumor stage specific effects and targets of TGFbeta1 expression. Preliminary studies reveal that TGFbeta1 expression in the normal epidermis, benign and malignant skin tumors provokes profoundly distinct responses from the host immune system that are associated with tumor regression or progression. The central hypothesis of this research proposal is that the changing roles of TGFbeta1 during cancer progression are linked to distinct responses of the immune system to tumor cell derived TGFbeta1. Specific Aim 1 tests the hypothesis that the adaptive immune response to epidermally derived TGFbeta1 is stage specific using genetic and immunological means to deplete and restore specific immune cell subsets. The second specific aim is to test the hypothesis that overexpression of TGFbeta1 in the normal epidermis and the resulting inflammation is a tumor-promoting stimulus for epidermal keratinocytes harboring a chemically or genetically activated ras oncogene. Specific Aim 3 tests the hypothesis that NF-kappaB signaling is essential for the stage specific response of the immune system to TGFbeta1 in the normal epidermis and in squamous tumors using in vitro and in vivo biochemical and molecular analysis, and genetic methods to block NF-kappaB signaling. The increased incidence of non-melanoma skin cancer in the general population, and the increasing problem of aggressive SCC of the skin in immunocompromised organ transplant patients represent a significant public health problem. The goal of this research project are to use this conditional expression mouse model to understand how TGFbeta1 produced by developing tumor cells differentially regulates the anti-tumor immune response, so that ultimately therapeutic targets and strategies can be identified that will block the immunosuppressive effects and enhance the anti-tumor inflammatory effects of tumor derived TGFbeta1.

描述（由申请人提供）：TGF β 1在人类癌症发展中具有肿瘤抑制和致癌作用，但这种功能变化的潜在机制仍然难以捉摸。 确定TGF β 1这些不同功能的机制以及这种变化如何发生将为癌症治疗提供重要的新靶点。 我们最近开发了一种TGF β 1条件性表皮表达小鼠模型，以确定肿瘤阶段特异性作用和TGF β 1表达的靶点。 初步研究表明，TGF β 1在正常表皮、良性和恶性皮肤肿瘤中的表达引起宿主免疫系统的显著不同的反应，这些反应与肿瘤的消退或进展有关。 这项研究的核心假设是，TGF β 1在癌症进展过程中的作用变化与免疫系统对肿瘤细胞来源的TGF β 1的不同反应有关。 特异性目的1检验了对表皮来源的TGF β 1的适应性免疫应答具有阶段特异性的假设，其使用遗传和免疫学手段消耗和恢复特异性免疫细胞亚群。 第二个具体的目的是测试的假设，过度表达TGF β 1在正常表皮和由此产生的炎症是一个肿瘤促进刺激表皮角质形成细胞窝藏化学或遗传激活的ras癌基因。 具体目标3使用体外和体内生物化学和分子分析以及遗传学方法来阻断NF-κ B信号传导，测试NF-κ B信号传导对于正常表皮和鳞状肿瘤中免疫系统对TGF β 1的阶段特异性应答是必不可少的这一假设。 一般人群中非黑色素瘤皮肤癌发病率的增加，以及免疫功能低下的器官移植患者皮肤侵袭性SCC问题的增加代表了一个重要的公共卫生问题。 该研究项目的目标是使用这种条件表达小鼠模型来了解肿瘤细胞产生的TGF β 1如何差异调节抗肿瘤免疫反应，从而最终确定治疗靶点和策略，以阻断免疫抑制作用并增强肿瘤源性TGF β 1的抗肿瘤炎症作用。