Sindbis Vectors For Advanced Pancreatic Cancer Therapy
用于先进胰腺癌治疗的 Sindbis 载体
基本信息
- 批准号:7413987
- 负责人:
- 金额:$ 28.67万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2004
- 资助国家:美国
- 起止时间:2004-07-01 至 2010-04-30
- 项目状态:已结题
- 来源:
- 关键词:AccountingAnimal ModelAnimalsApoptosisCancer EtiologyCellsCessation of lifeClassDataDeath RateDevelopmentDiagnosisDiseaseDisseminated Malignant NeoplasmDoseDrug KineticsEuropeGenerationsGoalsHumanImageImageryImaging TechniquesImmune responseImmune systemImmunocompetentIn VitroIn complete remissionIncidenceLeadLearningMagnetic Resonance ImagingMalignant neoplasm of pancreasMediatingModalityModelingMonitorMusNeoplasm MetastasisPatientsPlayReagentRoleSCID MiceSpecificityTestingTherapeuticTreatment ProtocolsUSSRUnited StatesViral VectorWorkbasecancer therapydesigngene therapyimprovedin vivomouse modelneoplastic cellnovelresponsetranslational approachtumorvector
项目摘要
DESCRIPTION (provided by applicant): In this application we seek to develop better vectors and reagents that will improve the therapy of pancreatic cancer. Pancreatic cancer is the fifth leading cause of cancer death in the US and accounts for approximately 29,000 deaths per year in the United States and 50,000 deaths per year in Europe (excluding the former USSR). Median survival is six months or less, and only four percent of patients are alive five years after diagnosis. Thus, incidence and death rates are virtually identical.
One approach to the treatment of this devastating disease is gene therapy. However, it is widely believed that gene therapy will not succeed until vectors are endowed with the ability to target tumor cells. As will be described in the application, Sindbis viral vectors can systemically target and specifically infect tumor cells in vivo. However, they require further study to enhance these capabilities.
To do so we seek to accomplish the following: (Aim 1) To use multiple imaging modalities, including IVlS, MRI, microCT, microSPECT, and microPET to monitor in vivo, in two different mouse models of pancreatic cancer, the extent and specificity of targeting and antitumor efficacy of various Sindbis vectors (generated in Aim 2). (Aim 2) To generate rationally designed Sindbis vectors that can be tested in the two animals models of Aim 1, with the goal of maximizing vector targeting and efficacy. The goal of Aim 2 is to design and develop Sindbis vectors that can induce complete remission in pancreatic cancers and their metastases through a combination of (a) the vector's known apoptosis-inducing potential, (b) the therapeutic payload they encode, and (c) their customizable targeting capabilities. In vivo monitoring of the targeting and efficacy of the new vectors, as discussed in Aim 1, will be critical to achieving this goal. (Aim 3) To examine the effects of the immune system on Sindbis-vector mediated therapy in an immunocompetent mouse model. Such studies will play a role in the design, generation and selection of Sindbis vectors created in Aim 2. (Aim 4) To perform pharmacokinetic studies with the Sindbis vectors to be used for vector-mediated therapy in immunocompetent mice. Such studies will help guide the design, generation and selection of Sindbis vectors created in Aim 2.
描述(由申请人提供):在本申请中,我们寻求开发将改善胰腺癌治疗的更好的载体和试剂。胰腺癌是美国癌症死亡的第五大原因,在美国每年约有29,000人死亡,在欧洲(不包括前苏联)每年约有50,000人死亡。中位生存期为6个月或更短,只有4%的患者在诊断后存活5年。因此,发病率和死亡率几乎相同。
治疗这种毁灭性疾病的一种方法是基因治疗。然而,人们普遍认为,只有赋予载体靶向肿瘤细胞的能力,基因治疗才能成功。如将在本申请中描述的,辛德毕斯病毒载体可以在体内全身靶向并特异性感染肿瘤细胞。但是,需要进一步研究,以提高这些能力。
(目的1)使用多种成像模式,包括IVIS、MRI、microCT、microSPECT和microPET,在胰腺癌的两种不同小鼠模型中体内监测各种辛德毕斯载体(在目的2中产生)的靶向程度和特异性以及抗肿瘤功效。(Aim 2)产生合理设计的辛德毕斯载体,其可以在目标1的两种动物模型中测试,目标是使载体靶向和功效最大化。目的2的目标是设计和开发辛德毕斯载体,其可以通过(a)载体的已知的诱导胰腺癌及其转移的潜力,(B)它们编码的治疗有效载荷,和(c)它们的可定制的靶向能力的组合来诱导胰腺癌及其转移的完全缓解。如目标1中所讨论的,体内监测新载体的靶向和功效对于实现这一目标至关重要。(Aim 3)在免疫活性小鼠模型中检查免疫系统对辛德毕斯载体介导的治疗的影响。这些研究将在目标2中创建的辛德毕斯载体的设计、生成和选择中发挥作用。(Aim 4)用辛德毕斯载体在免疫活性小鼠中进行药代动力学研究,以用于载体介导的治疗。这些研究将有助于指导目标2中创建的辛德毕斯载体的设计、生成和选择。
项目成果
期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
ATM kinase is activated by sindbis viral vector infection.
ATM 激酶被辛德毕斯病毒载体感染激活。
- DOI:10.1016/j.virusres.2012.03.008
- 发表时间:2012
- 期刊:
- 影响因子:5
- 作者:Pampeno,Christine;Hurtado,Alicia;Meruelo,Daniel
- 通讯作者:Meruelo,Daniel
Multiple functions of the 37/67-kd laminin receptor make it a suitable target for novel cancer gene therapy.
- DOI:10.1038/mt.2009.199
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:J. Scheiman;Jen-Chieh Tseng;Yun Zheng;D. Meruelo
- 通讯作者:J. Scheiman;Jen-Chieh Tseng;Yun Zheng;D. Meruelo
Interactions between laminin receptor and the cytoskeleton during translation and cell motility.
- DOI:10.1371/journal.pone.0015895
- 发表时间:2011-01-07
- 期刊:
- 影响因子:3.7
- 作者:Venticinque L;Jamieson KV;Meruelo D
- 通讯作者:Meruelo D
Interaction of human laminin receptor with Sup35, the [PSI⁺] prion-forming protein from S. cerevisiae: a yeast model for studies of LamR interactions with amyloidogenic proteins.
- DOI:10.1371/journal.pone.0086013
- 发表时间:2014
- 期刊:
- 影响因子:3.7
- 作者:Pampeno C;Derkatch IL;Meruelo D
- 通讯作者:Meruelo D
Sindbis viral vector induced apoptosis requires translational inhibition and signaling through Mcl-1 and Bak.
Sindbis 病毒载体诱导的细胞凋亡需要通过 Mcl-1 和 Bak 进行翻译抑制和信号传导。
- DOI:10.1186/1476-4598-9-37
- 发表时间:2010-02-12
- 期刊:
- 影响因子:37.3
- 作者:Venticinque L;Meruelo D
- 通讯作者:Meruelo D
{{
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 }}
DANIEL MERUELO其他文献
DANIEL MERUELO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('DANIEL MERUELO', 18)}}的其他基金
A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
针对突变负荷低、肿瘤浸润淋巴细胞少的肿瘤(例如卵巢癌)的一种新颖有效的免疫治疗方法
- 批准号:
10004922 - 财政年份:2020
- 资助金额:
$ 28.67万 - 项目类别:
A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
针对突变负荷低、肿瘤浸润淋巴细胞少的肿瘤(例如卵巢癌)的一种新颖有效的免疫治疗方法
- 批准号:
10417269 - 财政年份:2020
- 资助金额:
$ 28.67万 - 项目类别:
A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
针对突变负荷低、肿瘤浸润淋巴细胞少的肿瘤(例如卵巢癌)的一种新颖有效的免疫治疗方法
- 批准号:
10377711 - 财政年份:2020
- 资助金额:
$ 28.67万 - 项目类别:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
用于先进胰腺癌治疗的 Sindbis 载体
- 批准号:
7075406 - 财政年份:2004
- 资助金额:
$ 28.67万 - 项目类别:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
用于先进胰腺癌治疗的 Sindbis 载体
- 批准号:
6827190 - 财政年份:2004
- 资助金额:
$ 28.67万 - 项目类别:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
用于先进胰腺癌治疗的 Sindbis 载体
- 批准号:
6908073 - 财政年份:2004
- 资助金额:
$ 28.67万 - 项目类别:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
用于先进胰腺癌治疗的 Sindbis 载体
- 批准号:
7229427 - 财政年份:2004
- 资助金额:
$ 28.67万 - 项目类别:
IN VITRO INACTIVATION OF VIRUSES IN BLOOD COMPONENTS
血液成分中病毒的体外灭活
- 批准号:
2771384 - 财政年份:1995
- 资助金额:
$ 28.67万 - 项目类别:
相似海外基金
Quantification of Neurovasculature Changes in a Post-Hemorrhagic Stroke Animal-Model
出血性中风后动物模型中神经血管变化的量化
- 批准号:
495434 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Small animal model for evaluating the impacts of cleft lip repairing scar on craniofacial growth and development
评价唇裂修复疤痕对颅面生长发育影响的小动物模型
- 批准号:
10642519 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Bioactive Injectable Cell Scaffold for Meniscus Injury Repair in a Large Animal Model
用于大型动物模型半月板损伤修复的生物活性可注射细胞支架
- 批准号:
10586596 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
A Comparison of Treatment Strategies for Recovery of Swallow and Swallow-Respiratory Coupling Following a Prolonged Liquid Diet in a Young Animal Model
幼年动物模型中长期流质饮食后吞咽恢复和吞咽呼吸耦合治疗策略的比较
- 批准号:
10590479 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Diurnal grass rats as a novel animal model of seasonal affective disorder
昼夜草鼠作为季节性情感障碍的新型动物模型
- 批准号:
23K06011 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Longitudinal Ocular Changes in Naturally Occurring Glaucoma Animal Model
自然发生的青光眼动物模型的纵向眼部变化
- 批准号:
10682117 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
A whole animal model for investigation of ingested nanoplastic mixtures and effects on genomic integrity and health
用于研究摄入的纳米塑料混合物及其对基因组完整性和健康影响的整体动物模型
- 批准号:
10708517 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
A Novel Large Animal Model for Studying the Developmental Potential and Function of LGR5 Stem Cells in Vivo and in Vitro
用于研究 LGR5 干细胞体内外发育潜力和功能的新型大型动物模型
- 批准号:
10575566 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Elucidating the pathogenesis of a novel animal model mimicking chronic entrapment neuropathy
阐明模拟慢性卡压性神经病的新型动物模型的发病机制
- 批准号:
23K15696 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
The effect of anti-oxidant on swallowing function in an animal model of dysphagia
抗氧化剂对吞咽困难动物模型吞咽功能的影响
- 批准号:
23K15867 - 财政年份:2023
- 资助金额:
$ 28.67万 - 项目类别:
Grant-in-Aid for Early-Career Scientists














{{item.name}}会员




