Biomarker discovery in non-alcoholic steatohepatitis model mice
Biomarker discovery in non-alcoholic steatohepatitis model mice
批准号:
22790104
负责人:
TSUNODA Shin-ichi
金额:
$2.5万
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
项目状态:
已结题
起止时间:
2010 至 2011
中文摘要
非酒精性脂肪性肝炎(NASH)是近年来公认的一种代谢综合征相关疾病,是导致肝硬变和癌症的重要危险因素。在经济发达的国家,NASH患者的数量正在迅速增加。由于NASH的分子发病机制尚未明确,目前对NASH的准确诊断和有效治疗尚无定论。为了克服这种情况,我们通过使用NASH模型小鼠、CDAA喂养的小鼠或TSOD小鼠来寻找疾病相关蛋白。采用双向差示凝胶电泳法(2D-DGE)比较NASH模型小鼠和正常小鼠肝组织蛋白质组的差异。从凝胶中回收差异表达的蛋白质,用质谱仪进行鉴定。对这些蛋白的进一步分析将有助于阐明NASH发生的分子机制,并开发有前景的诊断和治疗方法。
英文摘要
Non-alcoholic steatohepatitis(NASH) is recently recognized as a metabolic syndrome-related disease and proved to be an important risk factor for liver cirrhosis and cancer. Number of patient with NASH is rapidly increasing in economically advanced countries. Since molecular pathogenesis of NASH has not been cleared, precise diagnosis and effective therapy for NASH has not been established yet. To overcome such a situation, we searched disease-related proteins by using NASH model mice, CDAA-fed mice or TSOD mice. Proteome of liver tissues of NASH model mice and normal mice were compared by 2-dimentional differential gel electrophoresis(2D-DIGE). Proteins of differential expression were recovered from the gel and then identified by mass spectrometer. Further analysis of these proteins would lead to elucidation of molecular mechanism of development of NASH and development of promising diagnosis and therapeutic methods.
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Proteomics-based analysis of non-alcoholic fatty liver disease (NAFLD) in mice
基于蛋白质组学的小鼠非酒精性脂肪肝病 (NAFLD) 分析
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[Watanabe T., Yamashita T., Nagano K., Kanasaki S., Yoshikawa T., Yoshioka Y., Itoh N., Abe Y., Kamada H., Tsutsumi Y., Tsunoda S.]
通讯作者:
Tsunoda S.
DOI:
10.1016/j.bbrc.2011.01.077
发表时间:
2011-02
期刊:
Biochemical and biophysical research communications
影响因子:
3.1
作者:
[Y. Yoshida;T. Yamashita;K. Nagano;S. Imai;H. Nabeshi;T. Yoshikawa;Y. Yoshioka;Y. Abe;H. Kamada;Y. Tsutsumi;S. Tsunoda]
通讯作者:
Y. Yoshida;T. Yamashita;K. Nagano;S. Imai;H. Nabeshi;T. Yoshikawa;Y. Yoshioka;Y. Abe;H. Kamada;Y. Tsutsumi;S. Tsunoda
抗体プロテオミクス技術による創薬ターゲットタンパク質の効率的探索
利用抗体蛋白质组学技术高效搜索药物发现靶蛋白
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Imai S., Nagano K., Yoshida Y., Okamura T., Yamashita T., Abe Y., Yoshikawa T., Yoshioka Y., Kamada H., Mukai Y., Nakagawa S., Tsutsumi Y., Tsunoda S., 梅原崇史, 角田慎一]
通讯作者:
角田慎一
Development of a novel antibody proteomics system using a phage antibody library for efficient screening of tumor-related biomarker proteins.
使用噬菌体抗体库开发新型抗体蛋白质组学系统,用于有效筛选肿瘤相关生物标志物蛋白质。
DOI:
--
发表时间:
2011
期刊:
Biomaterials 32(1)
影响因子:
--
作者:
[Imai S., Nagano K., Yoshida Y., Okamura T., Yamashita T., Abe Y., Yoshikawa T., Yoshioka Y., Kamada H., Mukai Y., Nakagawa S., Tsutsumi Y., Tsunoda S.]
通讯作者:
Tsunoda S.
Development of mutant IFN-alpha as a drug against the chemo-resistance of cancer stem cells
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批准号:26670061
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.41万
-
财政年份:2014
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负责人:TSUNODA Shin-ichi
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依托单位:
Drug target discovery for autoimmune diseases by using a technology creating functional mutant proteins
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批准号:24390022
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$11.9万
-
财政年份:2012
-
负责人:TSUNODA Shin-ichi
-
依托单位:
Proteomic analysis of tumor-derived nanovesicles and its application for innovative diagnostic method.
-
批准号:24650641
-
项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.5万
-
财政年份:2012
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负责人:TSUNODA Shin-ichi
-
依托单位:
海外基金