New Approaches to the Selective Targeting of Cancer-associated Fibroblasts

选择性靶向癌症相关成纤维细胞的新方法

• 批准号: 8461821
• 负责人: James Allen Van Deventer
• 金额: $ 4.92万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8461821
• 关键词: Antibodies; Behavior; Binding; Binding Proteins; Biological; Biological Assay; Biological Process; Biology; Breast; Cancer Biology; Cancer Model; Cancerous; Cell surface; Cells; Coculture Techniques; Collaborations; Colon; Communities; Development; Down-Regulation; Endothelial Cells; Epithelial Cells; Epitopes; Fibroblasts; Growth; Immune Tolerance; Immune system; In Vitro; Malignant Neoplasms; Mediating; Mus; Neoplasm Metastasis; Peptide Hydrolases; Phenotype; Play; Protease Inhibitor; Protein Engineering; Proteins; Reagent; Recruitment Activity; Research; Research Personnel; Role; Signal Transduction; Site; Solid Neoplasm; Stromal Cells; Surface; Techniques; Technology; Testing; Therapeutic; Therapeutic Effect; Therapeutic Studies; Tissues; Training; Tumor Cell Invasion; Work; Yeasts; angiogenesis; base; cancer cell; cancer therapy; cancer type; cell type; fibroblast activation protein alpha; fibroblast-activating factor; meetings; mouse model; neoplastic cell; novel strategies; novel therapeutics; prevent; research study; small molecule; success; therapeutic development; therapeutic target; tool; tumor; tumor growth; tumor initiation; tumor microenvironment; tumor progression

DESCRIPTION (provided by applicant): This research strives to develop protein-based therapeutics useful for the treatment of cancer built on the principle of eliminating key components of the solid tumor support network. In particular, this work will focus on the selective targeting of cancer-associated fibroblasts (CAFs). Cancer-associated fibroblasts have been implicated in a number of important roles in the initiation and progression of solid tumors, but selective targeting of these stromal cells with therapeutic effect has proven difficult. The most widely investigated approaches to selectively target CAFs take advantage of the nearly exclusive expression of the cell surface protease fibroblast activation protein-¿ (FAP) on the surfaces of CAFs located at the site of solid tumors. These efforts have focused on the development of antibodies and small molecules that target cells expressing FAP. However, these approaches have not yielded effective therapeutic cancer treatments. One potential reason for problems in the development of therapeutics that target CAFs via FAP is that the underlying biological role of FAP in tumor initiation and progression is still poorly understood. The work described here takes a combined approach to studying the biology of FAP and developing new cancer therapies. Three specific aims will be pursued in this project: 1) Develop binding proteins to multiple epitopes of the activated fibroblast cell surface protease fibroblast activation protein-¿ and use these binding proteins to construct multivalent antibody-based reagents. 2) Use multivalent antibody-based reagents developed in Aim 1, protease inhibitors targeting fibroblast activation protein-¿, or combinations of the two, in order to study the effect these reagents may have on fibroblast activation protein-¿-mediated functions in co-cultures of fibroblasts and cancer cells. 3) Use mouse models of cancer to examine the effects of reagents identified in Aim 2 on tumor growth and metastasis. The binding proteins to be generated as a part of Aim 1 will be developed using the protein engineering techniques afforded by yeast surface display. Multivalent binding proteins will combine identified binders within an antibody format. In vitro studies will primarily focus on the collective invasive behaviors of mixtures of tumor cells and CAFs and the behaviors of isolated pairs of tumor cells and CAFs using invasion assays and microwell array technology, respectively. Using binders developed in Aim 1, these studies will help elucidate which portions of FAP are responsible for invasive phenotypes and examine whether the selective downregulation of FAP expression on CAFs will inhibit these behaviors. Murine models of cancer will be used to study the therapeutic benefits of targeting FAP with multivalent binding proteins using experiments to test whether the proteins prevent tumor growth or prevent the development of immune system tolerance to a tumor. These studies will give the scientific community new tools for studying and interfering with the biological functions of FAP and new therapeutic leads for the treatment of cancer.

描述（由申请人提供）：本研究致力于开发基于消除实体肿瘤支持网络关键成分的原则的基于蛋白质的治疗方法，用于治疗癌症。特别是，这项工作将重点关注癌症相关成纤维细胞（CAFs）的选择性靶向。癌症相关成纤维细胞在实体瘤的发生和发展中起着重要作用，但选择性靶向这些具有治疗效果的基质细胞已被证明是困难的。选择性靶向CAFs的研究最广泛的方法是利用位于实体肿瘤部位的CAFs表面几乎完全表达的细胞表面蛋白酶成纤维细胞活化蛋白-¿（FAP）。这些努力集中在针对表达FAP的细胞的抗体和小分子的开发上。然而，这些方法还没有产生有效的治疗癌症的方法。通过FAP靶向cas的治疗方法发展中存在问题的一个潜在原因是FAP在肿瘤发生和发展中的潜在生物学作用仍然知之甚少。本文所描述的工作采用综合方法来研究FAP的生物学和开发新的癌症治疗方法。本项目将追求三个具体目标：1)开发活化成纤维细胞表面蛋白酶成纤维细胞活化蛋白-¿的多个表位结合蛋白，并利用这些结合蛋白构建基于多价抗体的试剂。2)使用Aim 1中开发的基于多价抗体的试剂，靶向成纤维细胞活化蛋白-¿的蛋白酶抑制剂，或两者的组合，以研究这些试剂对成纤维细胞活化蛋白-¿介导的成纤维细胞和癌细胞共培养功能的影响。3)利用小鼠肿瘤模型检测Aim 2中鉴定的试剂对肿瘤生长和转移的影响。作为Aim 1一部分的结合蛋白将利用酵母表面展示提供的蛋白质工程技术进行开发。多价结合蛋白将在抗体格式内结合已鉴定的结合物。体外研究将主要集中于肿瘤细胞和CAFs混合物的集体侵袭行为，以及分别使用侵袭试验和微孔阵列技术分离的肿瘤细胞和CAFs对的行为。使用Aim 1中开发的结合物，这些研究将有助于阐明FAP的哪些部分负责侵袭性表型，并检查cas上FAP表达的选择性下调是否会抑制这些行为。小鼠癌症模型将用于研究用多价结合蛋白靶向FAP的治疗效果，通过实验来测试这些蛋白是否能阻止肿瘤生长或阻止免疫系统对肿瘤产生耐受。这些研究将为科学界研究和干扰FAP的生物学功能提供新的工具，并为癌症治疗提供新的治疗线索。