Advanced research on cancer
癌症的高级研究
基本信息
- 批准号:11182101
- 负责人:
- 金额:$ 77.95万
- 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:1999
- 资助国家:日本
- 起止时间:1999 至 2004
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
This priority area, termed "Advanced research on cancer", is aimed at seeking cutting-edge cancer research by incorporating new technologies, disciplines and newly developing fields. In the past five years, much of the new insights have been gained about the mechanisms of oncogenic cell signaling and its suppression, particularly on the role of interferons and TGF-β, both of which function as negative regulator of cell growth. It also became possible to visualize behaviors of oncogene products in living cells and this is a new, important step to our understanding of cell transformation. New molecules have also been identified, which regulate cell adhesion and movement, and their functional analyses have been pursued; these include Claudins and WAVEs and these studies offered new insights in infiltration and metastasis of cancer cells. In addition, much progress has been made in understanding the mechanisms of apoptosis of cancerous cells and the clearance of such dying cells. It is particularly worth mentioning that one of the research project in this priority area spawned a new translational research project, that is, identification of HB-EGF as the target of ovarian cancers and application of CRM197, a mutant form of diphtheria toxin that inhibits HB-EGF, for therapy of this form of cancer. Overall, these achievements are represented in over several thousands of published papers, many of which appeared in journals such as Nature. Many collaborations with industries have been in progress with the aim of developing new drugs for cancer.
这一优先领域被称为“癌症高级研究”,旨在通过结合新技术、学科和新发展领域寻求尖端的癌症研究。在过去的五年中,关于肿瘤细胞信号传导及其抑制的机制,特别是干扰素和TGF-β的作用,获得了许多新的见解,它们都是细胞生长的负调节因子。在活细胞中可视化致癌基因产物的行为也成为可能,这是我们理解细胞转化的一个新的、重要的步骤。调控细胞粘附和运动的新分子也已被发现,并对其功能进行了分析;其中包括Claudins和WAVEs,这些研究为癌细胞的浸润和转移提供了新的见解。此外,在了解癌细胞凋亡的机制和对这些垂死细胞的清除方面也取得了很大进展。特别值得一提的是,该重点领域的一个研究项目催生了一个新的转化研究项目,即确定HB-EGF作为卵巢癌的靶点,并应用抑制HB-EGF的白喉毒素突变体CRM197治疗这种类型的癌症。总的来说,这些成果发表在数千篇论文中,其中许多发表在《自然》等杂志上。许多与工业界的合作正在进行中,目的是开发治疗癌症的新药。
项目成果
期刊论文数量(104)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Tsukita,Sh.: "Pores in the wall : Claudins constitute tight junction strands containing aqueouspores."J.Cell Biol.. 149巻. 13-16 (2000)
Tsukita,Sh.:“壁上的孔:Claudins 构成含有水孔的紧密连接链。”J.Cell Biol.. 149. 13-16 (2000)
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- 影响因子:0
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- 通讯作者:
Kubo H.: "Vascular Endothelial Growth Factor Receptor-3 is essential for maintenance of integrity of endothelial cell lining during tumor angiogenesis."Blood. 96巻. 546-553 (2000)
Kubo H.:“血管内皮生长因子受体 3 对于肿瘤血管生成过程中内皮细胞衬里的完整性的维持至关重要。”Blood. 96. 546-553 (2000)
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Adachi, M.: "Two co-existing mechanisms for nuclear import of MAP kinase: passive diffusion of a monomer and active transport of a dimer."EMBP Journal. 18. 5347-5358 (1999)
Adachi, M.:“MAP 激酶核输入的两种共存机制:单体的被动扩散和二聚体的主动运输。”EMBP 杂志。
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- 影响因子:0
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Mizuide, M., Hara, T., Furuya, T., Takeda, M., Kusanagi, K., Inada, Y., Mori, M., Imamura, T., Miyazawa, K., Miyazono, K.: "Two short segments of Smad3 are important for specific interaction of Smad3 with c-Ski and SnoN"J. Biol. Chem.. 278巻・1号. 531-536 (2
水出 M.、原 T.、古谷 T.、武田 M.、草薙 K.、稻田 Y.、森 M.、今村 T.、宫泽 K.、宫园 K.: “Smad3 的两个短片段对于 Smad3 与 c-Ski 和 SnoN 的特异性相互作用非常重要”J. Chem.. Vol. 278,No. 1. 531-536 (2)
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Toyoshima-Morimoto, F., Taniguchi, E., Nishida, E.: "Plk1 promotes nuclear translocation of human Cdc25C during prophase"EMBO Reports. (in press). (2002)
Toyoshima-Morimoto, F.、Taniguchi, E.、Nishida, E.:“Plk1 在前期促进人类 Cdc25C 的核转位”EMBO 报告。
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- 影响因子:0
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TANIGUCHI Tadatsugu其他文献
TANIGUCHI Tadatsugu的其他文献
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{{ truncateString('TANIGUCHI Tadatsugu', 18)}}的其他基金
Innate immune system activation and regulation via DNA receptors.
通过 DNA 受体激活和调节先天免疫系统。
- 批准号:
19209016 - 财政年份:2007
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Informatory expression system connecting cancer and immunity.
连接癌症和免疫的信息表达系统。
- 批准号:
17012005 - 财政年份:2005
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
New Frontiers of Cancer Sciences
癌症科学的新领域
- 批准号:
17012004 - 财政年份:2005
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Gene expression network for tumor suppression
抑制肿瘤的基因表达网络
- 批准号:
12219204 - 财政年份:2000
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Analysis of the genetic network in the host difence system.
宿主差异系统中的遗传网络分析。
- 批准号:
07407010 - 财政年份:1995
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Functional analysis of intracellular factors involved in the growth, differentiation, and transformation of lymphocytes
参与淋巴细胞生长、分化和转化的细胞内因子的功能分析
- 批准号:
04404034 - 财政年份:1992
- 资助金额:
$ 77.95万 - 项目类别:
Grant-in-Aid for General Scientific Research (A)
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