Targeting the ERK-MAP kinase pathway in cancer therapy
Targeting the ERK-MAP kinase pathway in cancer therapy
批准号:
17016056
负责人:
KOHNO Michiaki
金额:
$28.8万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
2005
资助国家:
日本
项目状态:
已结题
起止时间:
2005 至 2009
中文摘要
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英文摘要
Specific blockade of the ERK pathway by MEK inhibitors alone induces mostly cytostatic rather than pro-apoptotic effects, resulting in a limited therapeutic efficacy of MEK inhibitors. However, MEK inhibitors specifically enhance the induction of apoptosis by microtubule-destabilizing agents and HDAC inhibitors in various tumor cells with aberrant activation of the ERK pathway. Our results clearly indicate that administration of both a MEK inhibitor and a microtubule-destabilizing agent/HDAC inhibitor represents a promising chemotherapeutic strategy with improved safety for cancer patients.
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Enantioselective total synthesis of (+)- Ottelione A, (-)-Ottelione B, (+)-3-epi- Otterlione A and preliminary evaluation of antitumor activity.
( )-Ottelione A、(-)-Ottelione B、( )-3-epi- Otterlione A 的对映选择性全合成及抗肿瘤活性初步评价。
DOI:
--
发表时间:
2007
期刊:
Chem. Eur. J. 13
影响因子:
--
作者:
[Araki, H., Inoue, M., Suzuki, T., Yamori, T., Kohno, M., Watanabe, K., Abe, H., Katoh, T.]
通讯作者:
T.
Blockade of the PI3-kinase-Akt signaling pathway enhances induction of apoptosis by microtubule- destabilizing agents in tumor cells in which the pathway is constitutively activated.
PI3-激酶-Akt 信号通路的阻断可增强肿瘤细胞中微管不稳定剂对细胞凋亡的诱导,其中该通路被组成型激活。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Watanabe, K., Fujiwara, Y., Tanimura, S., Ozaki, K, Kohno, M.]
通讯作者:
M.
がんの分子標的治療(鶴尾隆編集)
癌症分子靶向治疗(鹤夫隆主编)
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[近藤科江, 平岡真寛, 河野通明(分担執筆)]
通讯作者:
河野通明(分担執筆)
低酸素環境下における癌細胞の抗癌剤耐性獲得の分子機構
缺氧环境下癌细胞抗癌药物产生耐药性的分子机制
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[Tsuda H.et al., Hamada H., 尾崎恵一, 濱田洋文, 濱田洋文, 尾崎恵一]
通讯作者:
尾崎恵一
DOI:
10.1016/j.bbrc.2005.11.131
发表时间:
2006-01-27
期刊:
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
影响因子:
3.1
作者:
[Ozaki, K, Minoda, A, Kohno, M]
通讯作者:
Kohno, M
共 33 条
Targeting the ERK-MAP kinase pathway in cancer therapy
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批准号:22300340
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.23万
-
财政年份:2010
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负责人:KOHNO Michiaki
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依托单位:
Role of MAP kinase cascades in the regulation of diverse cellular functions
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批准号:17390020
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.6万
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财政年份:2005
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负责人:KOHNO Michiaki
-
依托单位:
Role of MAP Kinase Cascade in the Regulation of Diverse Cellular Functions
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批准号:14370747
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.9万
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财政年份:2002
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负责人:KOHNO Michiaki
-
依托单位:
Development of specific inhibitors against MAP kinase pathways
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批准号:11557185
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.7万
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财政年份:1999
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负责人:KOHNO Michiaki
-
依托单位:
Role of MAP Kinase Cascade in the Regulation of Diverse Cellular Fuctions.
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批准号:10470485
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项目类别:Grant-in-Aid for Scientific Research (B).
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资助金额:$8.45万
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财政年份:1998
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负责人:KOHNO Michiaki
-
依托单位:
Role of the ERK MAP Kinase Cascade in the Regulation of Cell Proliferation and Differentiation.
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批准号:08457613
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$4.93万
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财政年份:1996
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负责人:KOHNO Michiaki
-
依托单位:
Development of anti-skin ulcer drug based on the new concept -Application of the stimulatory effect of TNF-alpha on the production of NGF in fibroblasts
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批准号:07557378
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项目类别:Grant-in-Aid for Scientific Research (A)
-
资助金额:$2.3万
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财政年份:1995
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负责人:KOHNO Michiaki
-
依托单位:
Regulation of mitogenic signaling pathways which involve the function of GTP-binding protein-Possible involvement of protein tyrosine phosphorylation.
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批准号:02808035
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$0.96万
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财政年份:1990
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负责人:KOHNO Michiaki
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依托单位:
海外基金