Harnessing the Multipotency of Cancer Stem Cells for Differentiation Therapy
利用癌症干细胞的多能性进行分化治疗
基本信息
- 批准号:8692120
- 负责人:
- 金额:$ 22.12万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-09-18 至 2016-08-31
- 项目状态:已结题
- 来源:
- 关键词:2,4-thiazolidinedioneAdipocytesAdolescentAffectAgonistAutomobile DrivingBenignBiological AssayCell LineageCell ProliferationCellsChildChildhoodClinicDevelopmentDiabetes MellitusDifferentiation TherapyDiseaseDrug usageFDA approvedFatty acid glycerol estersGenesGrowthHumanIncidenceInsulinLeadMalignant Bone NeoplasmMalignant NeoplasmsMesenchymalMesenchymal Cell NeoplasmMesenchymal Stem CellsMetastatic OsteosarcomaMusOperative Surgical ProceduresOsteoblastsOutcomePPAR gammaPathway interactionsPatientsPeroxisome Proliferator-Activated ReceptorsPharmaceutical PreparationsPhenotypePioglitazonePopulationProliferatingPropertyRecurrenceRecurrent diseaseRegimenRelapseResearchSafetyStagingStem cellsSurvival RateTeenagersTestingTherapeuticThiazolidinedionesTissuesTumor SuppressionTumorigenicityUndifferentiatedWorkalternative treatmentbasebonebone cellcancer cellcancer stem cellclinically significantimprovedlimb amputationlipid biosynthesisneoplastic cellnovelnovel strategiesnovel therapeuticsosteoprogenitor cellosteosarcomaoutcome forecastprogenitorpublic health relevancerosiglitazonestemstem cell differentiationtumortumor growthtumorigenic
项目摘要
DESCRIPTION (provided by applicant): Osteosarcoma is an aggressive bone cancer that affects children and adolescents. Osteosarcoma is considered a disease of disrupted differentiation wherein tumor cells are unable to differentiate into proper bone-forming mature osteoblasts. Osteosarcoma is often advanced at presentation and current treatments consist primarily of chemotherapeutic regimens and surgery. Osteosarcoma has a high rate of recurrence and often leads to limb amputations in young patients. The survival rate for metastatic osteosarcoma remains around 30% and alternative treatments are badly needed for this devastating disease. In this collaborative study, we propose to test a novel approach for treating osteosarcoma by harnessing intrinsic multipotency features of the osteosarcoma cancer stem cells. Osteosarcomas arise from mesenchymal stem cells that normally have the ability to form bone and fat cells. Our differentiation therapy approach is to use agents that preferentially inhibit the growth of osteosarcoma cancer stem cells while steering them to become adipocytes. We will use a class of drugs, the TZDs, that are agonists for PPAR?, the master regulator of adipogenesis. Several TZDs are approved for their unrelated effect in insulin clearance and treatment of diabetes. We have found that TZDs can inhibit the growth of osteosarcoma cells and promote adipogenic differentiation. We will test the effects of TZD on primary mouse and human osteosarcoma cells in mice, and examine their effects on cells and tumors. In particular, we will determine whether the TZDs can activate genes needed for adipogenesis. If successful, this proposal will provide the basis for new strategies to treat osteosarcoma in the clinic.
描述(由申请人提供):骨肉瘤是一种影响儿童和青少年的侵略性骨癌。骨肉瘤被认为是一种破坏分化的疾病,其中肿瘤细胞无法分化为适当的骨形成成熟成骨细胞。骨肉瘤通常在表现上进行进展,目前的治疗主要由化学治疗方案和手术组成。骨肉瘤的复发率很高,并且经常导致年轻患者的肢体截肢。转移性骨肉瘤的存活率仍然约为30%,这种毁灭性疾病的替代治疗迫切需要替代治疗。 在这项合作研究中,我们建议通过利用骨肉瘤癌症干细胞的内在多能特征来测试一种治疗骨肉瘤的新方法。骨肉瘤来自通常具有形成骨骼和脂肪细胞的能力的间充质干细胞。我们的分化治疗方法是使用优先抑制骨肉瘤干细胞生长的药物,同时引导它们成为脂肪细胞。 我们将使用一类药物,即TZD,是脂肪生成的主要调节剂PPAR的激动剂。几个TZD在胰岛素清除和糖尿病治疗中的无关效应批准。我们发现TZD可以抑制骨肉瘤细胞的生长并促进脂肪分化。我们将测试TZD对小鼠原代小鼠和人骨肉瘤细胞的影响,并检查它们对细胞和肿瘤的影响。特别是,我们将确定TZD是否可以激活脂肪形成所需的基因。如果成功,该提案将为治疗诊所中骨肉瘤的新策略提供基础。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Alka Mansukhani其他文献
Alka Mansukhani的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Alka Mansukhani', 18)}}的其他基金
Harnessing the Multipotency of Cancer Stem Cells for Differentiation Therapy
利用癌症干细胞的多能性进行分化治疗
- 批准号:
8929179 - 财政年份:2014
- 资助金额:
$ 22.12万 - 项目类别:
相似国自然基金
脂肪干细胞外泌体miRNA-299a-3p调控巨噬细胞Thbs1缓解脂肪组织衰老的机制研究
- 批准号:82301753
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
肝细胞因子ORM2通过抑制Kupffer细胞激活改善非酒精性脂肪性肝炎的作用及机制研究
- 批准号:82300966
- 批准年份:2023
- 资助金额:20 万元
- 项目类别:青年科学基金项目
CD36/FABP4/CPT1轴介导脂肪酸转运促进白血病干细胞的维持在白血病化疗耐药中的作用及机制研究
- 批准号:82300206
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
放射后早期神经元-星形胶质细胞脂肪酸代谢耦联对正常脑组织免疫微环境的重塑及其机制研究
- 批准号:82373516
- 批准年份:2023
- 资助金额:49 万元
- 项目类别:面上项目
高原低氧上调肝脏ANGPTL4基因的表达导致巨噬细胞M1/M2比例失衡从而促进肝脂肪化的机制研究
- 批准号:82360333
- 批准年份:2023
- 资助金额:32 万元
- 项目类别:地区科学基金项目
相似海外基金
Pathophysiology of Metabolic Defects of Juvenile Obesity
青少年肥胖代谢缺陷的病理生理学
- 批准号:
7262561 - 财政年份:2001
- 资助金额:
$ 22.12万 - 项目类别:
Pathophysiology of Metabolic Defects of Juvenile Obesity
青少年肥胖代谢缺陷的病理生理学
- 批准号:
7673289 - 财政年份:2001
- 资助金额:
$ 22.12万 - 项目类别:
Pathophysiology of Metabolic Defects of Juvenile Obesity
青少年肥胖代谢缺陷的病理生理学
- 批准号:
7477277 - 财政年份:2001
- 资助金额:
$ 22.12万 - 项目类别: