Mesenchymal stem cells infected with modified adenoviruses as carrier cells that target human gastrointestinal tumors
感染修饰腺病毒的间充质干细胞作为靶向人类胃肠道肿瘤的载体细胞
基本信息
- 批准号:20591585
- 负责人:
- 金额:$ 3万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:2008
- 资助国家:日本
- 起止时间:2008 至 2010
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Majority of human solid tumors, when clinically in an advanced stage, is resistant to most of conventional therapies and consequently improved prognosis with a novel strategy is a crucial target in clinical settings. We developed type 5 adenoviruses which replicated preferentially within tumors and then examined the anti-tumor effects. We also modified the adenoviruses of which the receptor-binding site was replaced with that of type 35 adenoviruses, which subsequently increased the infectivity to human tumors due to a high receptor expression in the tumors. We examined a possible advantage to use carrier cells which were infected with such adenoviruses.
大多数人类实体瘤在临床上处于晚期时,对大多数常规疗法都有抵抗力,因此通过新策略改善预后是临床环境中的一个关键目标。我们开发了5型腺病毒,它优先在肿瘤内复制,然后检查其抗肿瘤作用。我们还对腺病毒进行了修饰,将其受体结合位点替换为35型腺病毒,由于肿瘤中受体的高表达,从而增加了对人类肿瘤的感染性。我们研究了使用感染此类腺病毒的载体细胞的可能优势。
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)
Cancer Gene Therapy
- DOI:10.1177/153303460500400402
- 发表时间:2005-02
- 期刊:
- 影响因子:2.8
- 作者:Masato Yamamoto;D. Curiel
- 通讯作者:Masato Yamamoto;D. Curiel
Cytotoxicity of adenoviruses expressing the wild-type p53 gene to esophageal carcinoma cells is linked with the CAR expression level and indirectly with the endogenous p53 status
- DOI:10.1038/cgt.2009.21
- 发表时间:2009-11-01
- 期刊:
- 影响因子:6.4
- 作者:Ma, G.;Kawamura, K.;Tagawa, M.
- 通讯作者:Tagawa, M.
Anti-tumor effects produced by the combinatory use of E1B-55 kDa-deleted adenoviruses and chemotherapeutic agents for human esophageal carcinoma cells.
E1B-55 kDa 缺失腺病毒与化疗药物联合使用对人食管癌细胞产生抗肿瘤作用。
- DOI:
- 发表时间:2008
- 期刊:
- 影响因子:0
- 作者:Guangyu Ma;et al
- 通讯作者:et al
Combinatory cytotoxic effects produced by E1B-55kDa-deleted adenoviruses and chemotherapeutic agents are dependent on the agents in esophageal carcinoma.
- DOI:10.1038/cgt.2010.37
- 发表时间:2010-11
- 期刊:
- 影响因子:6.4
- 作者:
- 通讯作者:
Interferon-λ induces G1 phase arrest or apoptosis in esophageal carcinoma cells and produces anti-tumor effects in combination with anti-cancer agents.
干扰素-λ可诱导食管癌细胞G1期阻滞或凋亡,并与抗癌药物联合产生抗肿瘤作用。
- DOI:
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:Li Q.;Kawamura K.;Ma G.;Iwata F.;Numasaki M.;Suzuki N.;Shimada H.;Tagawa M.
- 通讯作者:Tagawa M.
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TAGAWA Masatoshi其他文献
TAGAWA Masatoshi的其他文献
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{{ truncateString('TAGAWA Masatoshi', 18)}}的其他基金
Molecular therapy for esophageal cancer targeting the p53 and the Hippo pathways
针对 p53 和 Hippo 通路的食管癌分子治疗
- 批准号:
17K10617 - 财政年份:2017
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Combinatory use of replication-competent adenoviruses and chemotherapeutic agents produces anti-tumor effects on human esophageal carcinoma cells
具有复制能力的腺病毒与化疗药物联合使用对人食管癌细胞产生抗肿瘤作用
- 批准号:
23591951 - 财政年份:2011
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Oncolytic adenovirus modified to increase its infectivity for gastrointestinal cancer
溶瘤腺病毒经过修饰以增加其对胃肠道癌症的感染性
- 批准号:
16591381 - 财政年份:2004
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Gene therapy for gastrointestinal tumors using antigen presenting cells activated with gene transfer
使用通过基因转移激活的抗原呈递细胞进行胃肠道肿瘤的基因治疗
- 批准号:
13671367 - 财政年份:2001
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Suicide gene therapy for gastrointestinal tumors using tumor-specific promoters
使用肿瘤特异性启动子进行胃肠道肿瘤的自杀基因治疗
- 批准号:
11671298 - 财政年份:1999
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Immune gene therapy for gastrointestinal cancer by activation Th1-type helper T cells.
通过激活 Th1 型辅助 T 细胞对胃肠癌进行免疫基因治疗。
- 批准号:
09671281 - 财政年份:1997
- 资助金额:
$ 3万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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- 批准号:
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- 资助金额:
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- 批准号:
18K15323 - 财政年份:2018
- 资助金额:
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