Development of new functional artificial virus contained cancer-selective anticancer drug with the cancer-specific molecules
开发含有癌症特异性分子的癌症选择性抗癌药物的新型功能性人工病毒
基本信息
- 批准号:22791255
- 负责人:
- 金额:$ 2.58万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Young Scientists (B)
- 财政年份:2010
- 资助国家:日本
- 起止时间:2010 至 2011
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
We can create a multi-functional artificial virus contained cancer-specific anti-cancer drug. We also evaluated the form and function of this new virus in vitro. We confirmed that artificial virus had been specifically-taken into the pancreatic cancer cell line and had a certain therapeutic effect in comparative experiments in pancreatic cancer cell lines and normal cells in vitro.
我们可以创造一种多功能的人工病毒包含癌症特异性抗癌药物。我们还在体外评估了这种新病毒的形式和功能。通过对胰腺癌细胞株和正常细胞的体外对比实验,证实了人工病毒已特异性地进入胰腺癌细胞株,并具有一定的治疗作用。
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)
Adenoviral Therapy Is More Effective in Gemcitabine-resistant Pancreatic Cancer than in Gemcitabine-sensitive Cells.
腺病毒治疗对吉西他滨耐药的胰腺癌比对吉西他滨敏感的细胞更有效。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:Takaharu Yasui;Kenoki Ohuchida;Ming Zhao;Lin Cui;Manabu Onimaru;Takuya Egami;Hayato Fujita;Takao Ohtsuka;Kazuhiro Mizumoto;Kunio Matsumoto;Masao Tanaka.
- 通讯作者:Masao Tanaka.
Tumor–stroma interactions reduce the efficacy of adenoviral therapy through the HGF‐MET pathway
- DOI:10.1111/j.1349-7006.2010.01783.x
- 发表时间:2011-02
- 期刊:
- 影响因子:5.7
- 作者:T. Yasui;K. Ohuchida;Ming Zhao;M. Onimaru;Takuya Egami;H. Fujita;T. Ohtsuka;K. Mizumoto;Masao Tanaka
- 通讯作者:T. Yasui;K. Ohuchida;Ming Zhao;M. Onimaru;Takuya Egami;H. Fujita;T. Ohtsuka;K. Mizumoto;Masao Tanaka
Gencitabime synergistically enhances the effect of adenovirus gene therapy through activation of the CMV promoter in
Gencitabime 通过激活 CMV 启动子来协同增强腺病毒基因治疗的效果
- DOI:
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:Onimaru M;Ohuchida K;Egami T;Mizumoto K;Nagai E;Cui L;Toma H;Matsumoto K;Hashizume M;Tanaka M.
- 通讯作者:Tanaka M.
Combination with low-dose gemcitabine andhTERT-promoter-dependent conditionally replicative adenovirus enhances cytotoxicity through their crosstalk mechanisms in pancreatic cancer
与低剂量吉西他滨和 hTERT 启动子依赖性条件复制腺病毒联合使用,通过其串扰机制增强胰腺癌中的细胞毒性
- DOI:
- 发表时间:2010
- 期刊:
- 影响因子:9.7
- 作者:Onimaru M;Ohuchida K;Nagai E,Mizumoto K;Egami T;Tanaka M
- 通讯作者:Tanaka M
Tanaka M Predicting the chemosensitivity of pancreatic cancer cells by quantifying the expression levels of genes associated with the metabolism of gemcitabine and 5-fluorouracil
Tanaka M 通过量化与吉西他滨和 5-氟尿嘧啶代谢相关的基因的表达水平来预测胰腺癌细胞的化疗敏感性
- DOI:
- 发表时间:2011
- 期刊:
- 影响因子:5.2
- 作者:Kurata N;Fujita H;Ohuchida K;Mizumoto K;Mahawithitwong P;Sakai H;Onimaru M;Manabe T;Ohtsuka T
- 通讯作者:Ohtsuka T
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{{ truncateString('ONIMARU Manabu', 18)}}的其他基金
Elucidation of the mechanism of anti-tumor effect by disabling the immune escape mechanism and development of treatment based on regulation of the pancreatic cancer microenvironment
阐明通过阻断免疫逃逸机制的抗肿瘤作用机制并开发基于胰腺癌微环境调节的治疗方法
- 批准号:
20K07678 - 财政年份:2020
- 资助金额:
$ 2.58万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Clarification and control of immune cell-induced PSC substrate remodeling using KPCL mice
使用 KPCL 小鼠澄清和控制免疫细胞诱导的 PSC 底物重塑
- 批准号:
17K10700 - 财政年份:2017
- 资助金额:
$ 2.58万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Elucidation of selection mechanism of disseminated cancer cells in metastatic organs
阐明转移器官中播散性癌细胞的选择机制
- 批准号:
26462064 - 财政年份:2014
- 资助金额:
$ 2.58万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Elucidation of the radioresistance mechanism on the microenviroment of pancreatic cancer and control of the stroma cells causing radioresistance by newly artificial virus.
阐明胰腺癌微环境的放射抗性机制以及新型人工病毒对引起放射抗性的基质细胞的控制。
- 批准号:
24791431 - 财政年份:2012
- 资助金额:
$ 2.58万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
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