Role of Fibroblasts in Cancer
成纤维细胞在癌症中的作用
基本信息
- 批准号:7655275
- 负责人:
- 金额:$ 25.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-07-10 至 2011-05-31
- 项目状态:已结题
- 来源:
- 关键词:AblationAddressAllelesAngiogenic SwitchApplications GrantsAttenuatedBiochemicalBiologicalBreast Cancer CellCancer ModelCarcinomaCellsCytoskeletal ProteinsDataEndothelial CellsEnvironmentExtracellular MatrixExtracellular Matrix ProteinsExtracellular ProteinFamilyFibroblastsGeneticGrowthGrowth FactorHealedKnowledgeLaboratoriesLiverLungMalignant NeoplasmsMammary NeoplasmsMediatingMediator of activation proteinMetastatic LesionMetastatic Neoplasm to the LiverMethodsModelingMusMutant Strains MiceNeoplasm MetastasisNodulePericytesPhenotypePlayPopulationPopulation HeterogeneityPrimary NeoplasmProductionProteinsResearchRestRoleSeedsSmooth Muscle Actin Staining MethodSoilStromal Cell-Derived Factor 1TechniquesTenascinTestingThymidine KinaseTimeTransgenic MiceVascular Endothelial Growth FactorsVascular Permeabilitiesangiogenesiscancer cellcell motilitychemokinedensitydesignhealinginsightmouse Fsp1 proteinmouse modelpromoterreconstitutionresearch studyresponse to injurytumortumor growthtumor progression
项目摘要
DESCRIPTION (provided by applicant): Tumors are known as wounds that do not heal - implying that cells involved in angiogenesis and injury response, such as endothelial cells and fibroblasts, have a prominent role in the progression, growth and spread of cancers. Our knowledge regarding the role of the resting and the activated fibroblasts (also known as carcinoma-associated fibroblasts, CAF) in cancer is still evolving. Fibroblast production of growth factors, chemokines and extracellular matrix likely facilitates the angiogenic recruitment of endothelial cells and pericytes. Moreover, the precise role of fibroblasts in the recruitment and the formation of metastasis is completely unknown. Therefore, this grant application is focused on the role of fibroblast in cancer progression, with specific emphasis on metastasis. Emerging data from other laboratories and our own preliminary data suggest that fibroblasts are a heterogeneous population. In the tumor microenvironment, we have now identified a population of CAF that are positive for fibroblast specific protein-1 (FSP1) but not for alpha-smooth muscle actin (aSMA). Our studies demonstrate for the first time that not all CAF are aSMA+. Additionally, specific ablation of FSP1+/alphaSMA- fibroblasts using transgenic mice, which harbor FSP1 promoter driven thymidine kinase protein (FSP1-tk), demonstrate that FSP1+ fibroblasts are critical for the formation of metastasis without a significant impact on the growth of angiogenic primary tumors. Furthermore, we demonstrate that VEGF, SDF-1 and Tenascin-C, might mediate the formation of metastatic nodules. To further evaluate the role of these fibroblasts in the formation of metastasis, we propose the following aims in this proposal: 1. To evaluate the contribution of FSP1+ fibroblasts in the growth of primary tumors and recruitment of metastasis, 2. To address the contribution of VEGF produced by FSP1+ fibroblasts in the growth of primary tumors and the formation of metastasis, 3. To investigate the contribution of SDF-1, produced by FSP1+ fibroblasts, a downstream effector of VEGF, in the formation of metastasis, and 4. To study the contribution of Tenascin-C, a FSP1+ fibroblast-produced extracellular matrix protein, in the organization of metastasis nodules. Successful completion of experiments proposed in this grant application will provide crucial insights into the role of FSP1+ fibroblasts as key determinants for the organization of metastasis. PUBLIC HEARLTH RELEVANCE: Cancer cells are not the only constituent cells within a primary tumor and secondary metastasis. Other cells including fibroblasts are found inside the primary tumor and secondary metastatic nodules. The role of such fibroblasts in cancer progression and metastasis is unknown. This proposal addresses the role of fibroblasts in facilitating metastasis.
描述(由申请人提供):肿瘤被称为无法愈合的伤口 - 表明参与血管生成和损伤反应的细胞,例如内皮细胞和成纤维细胞,在癌症的进展,生长和扩散中具有重要作用。 我们对静息和活化成纤维细胞的作用(也称为癌相关的成纤维细胞CAF)在癌症中的知识仍在发展。 成纤维细胞的生长因子,趋化因子和细胞外基质的产生可能促进内皮细胞和周细胞的血管生成募集。 此外,成纤维细胞在募集中的确切作用和转移的形成是完全未知的。 因此,该赠款的应用集中在成纤维细胞在癌症进展中的作用,并特别强调转移。 来自其他实验室和我们自己的初步数据的新兴数据表明,成纤维细胞是异质的人群。 在肿瘤微环境中,我们现在已经确定了成纤维细胞特异性蛋白-1(FSP1)阳性的CAF人群,但对α-平滑肌肌动蛋白(ASMA)均不为阳性。 我们的研究首次表明并非所有CAF都是ASMA+。 此外,使用转基因小鼠的FSP1+/alphase-成纤维细胞的特异性消融,携带FSP1启动子驱动的胸苷激酶蛋白(FSP1-TK)的特异性消融表明,FSP1+成纤维细胞对转移的形成至关重要,而没有对血管生成原始肿瘤生长产生重大影响。 此外,我们证明VEGF,SDF-1和Tenascin-C可能介导转移性结节的形成。 为了进一步评估这些成纤维细胞在转移形成中的作用,我们提出以下目的是在此提案中的目的:1。评估FSP1+成纤维细胞在原发性肿瘤生长中的贡献和转移的募集的贡献,2。旨在解决FSP1+ Fibroblasts在FIBROBLOBLOBLASTS中的贡献。 SDF-1由FSP1+成纤维细胞(VEGF的下游效应子)在转移的形成和4中产生的贡献。研究Tenascin-C(一种FSP1+成纤维细胞产生的细胞外基质蛋白)在Metastasis Nodules的组织中的贡献。 成功完成本赠款应用程序中提出的实验将为FSP1+成纤维细胞作为转移组织的关键决定因素的作用提供关键见解。 公共呼吸道相关性:癌细胞并不是原发性肿瘤和继发转移中唯一的组成细胞。 在原发性肿瘤和继发转移结节内发现了其他细胞,包括成纤维细胞。 这种成纤维细胞在癌症进展和转移中的作用尚不清楚。 该建议探讨了成纤维细胞在促进转移中的作用。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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RAGHU KALLURI其他文献
RAGHU KALLURI的其他文献
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$ 25.5万 - 项目类别:
Mechanisms associated with organotropic metastasis
与器官转移相关的机制
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Mechanisms associated with organotropic metastasis
与器官转移相关的机制
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10532826 - 财政年份:2021
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