Sindbis Vectors For Advanced Pancreatic Cancer Therapy
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
批准号:
7413987
负责人:
DANIEL MERUELO
金额:
$28.67万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-07-01 至 2010-04-30
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
中文摘要
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英文摘要
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.
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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:
Virus research
影响因子:
5
作者:
[Pampeno,Christine, Hurtado,Alicia, Meruelo,Daniel]
通讯作者:
Meruelo,Daniel
DOI:
10.1038/mt.2009.199
发表时间:
2010
期刊:
Molecular therapy : the journal of the American Society of Gene Therapy
影响因子:
--
作者:
[J. Scheiman;Jen-Chieh Tseng;Yun Zheng;D. Meruelo]
通讯作者:
J. Scheiman;Jen-Chieh Tseng;Yun Zheng;D. Meruelo
DOI:
10.1371/journal.pone.0015895
发表时间:
2011-01-07
期刊:
PloS one
影响因子:
3.7
作者:
[Venticinque L, Jamieson KV, Meruelo D]
通讯作者:
Meruelo D
DOI:
10.1371/journal.pone.0086013
发表时间:
2014
期刊:
PloS one
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:
Molecular cancer
影响因子:
37.3
作者:
[Venticinque L, Meruelo D]
通讯作者:
Meruelo D
共 6 条
A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
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批准号:10004922
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项目类别:
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资助金额:$40.0万
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财政年份:2020
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负责人:DANIEL MERUELO
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依托单位:
A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
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批准号:10417269
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资助金额:$86.67万
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A novel and effective immunotherapeutic approach for tumors with a low mutational load and few tumor-infiltrating lymphocytes, such as ovarian cancer
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批准号:10377711
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项目类别:
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资助金额:$113.33万
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财政年份:2020
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负责人:DANIEL MERUELO
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依托单位:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
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批准号:7075406
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项目类别:
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资助金额:$29.52万
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财政年份:2004
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依托单位:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
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批准号:6827190
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资助金额:$31.96万
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批准号:6908073
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资助金额:$30.23万
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依托单位:
Sindbis Vectors For Advanced Pancreatic Cancer Therapy
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批准号:7229427
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资助金额:$28.67万
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财政年份:2004
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负责人:DANIEL MERUELO
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TARGETED IN VIVO GENE THERAPY FOR BRAIN TUMORS
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资助金额:$36.77万
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资助金额:$27.39万
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海外基金