课题基金 / 基金详情

Search for Novel Anti-cancer Drugs Targetting DNA Replication and Repair

Search for Novel Anti-cancer Drugs Targetting DNA Replication and Repair
寻找针对 DNA 复制和修复的新型抗癌药物
批准号:
08557131
负责人:
HANAOKA Fumio
金额:
$9.15万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
1996
资助国家:
日本
项目状态:
已结题
起止时间:
1996 至 1997

项目摘要

项目成果

HANAOKA Fumio的其他基金

相似基金

相关文献

中文摘要
翻译
我们使用无细胞系统对放线菌和真菌菌进行SV40 DNA复制和紫外照射SV40小染色体核苷酸切除修复(NER)的培养上清液进行筛选,获得DNA复制和修复的抑制剂或刺激物。作为这些筛选的结果,我们获得了一些复制抑制剂和NER抑制剂的样品。纯化了其中一个复制抑制剂RK606,其结构鉴定为大豆皂苷(soyasaponin II)的一种。RK606还可以抑制SV40 DNA与纯化蛋白的复制,因此,我们研究了RK606对单个酶和蛋白的影响。结果表明,RK606特异性抑制sv40t抗原的DNA解旋酶活性。有趣的是,细胞DNA解旋酶未被该化合物抑制,这表明RK606可能是T抗原解旋酶的特异性抑制剂。据我们所知,这是除ATP类似物外的第一个DNA解旋酶抑制剂。研究了其中一种修复抑制剂RK679在不同pH下的稳定性和几种溶剂的可萃取性。修复抑制剂的行为与某些酪氨酸激酶抑制剂染料木素和大豆苷元的行为相似,因此,我们检查了这些酪氨酸激酶抑制剂对无细胞NER的影响。然而,我们没有发现这些化合物对NER有任何影响,这表明RK679既不是染料木素也不是大豆苷元,而是不同的化合物。
英文摘要
We have screened more than one hundred of culture supernatants of Actinomycetes and Eumycetes using cell-free systems for SV40 DNA replication and the nucleotide excision repair (NER) with UV-irradiated SV40 minichromosomes to obtain either inhibitors or stimulators for DNA replication and repair. As s result of these screening, we obtained a couple of samples for replication inhibitors and NER inhibitors.One of the replication inhibitors (RK606) was purified, and its structure was identified as a kind of soybean saponin (soyasaponin II). RK606 also inhibited SV40 DNA replication with purified proteins, therefore, we examined the effect of RK606 on individual enzymes and proteins. It turned out that RK606 specifically inhibited DNA helicase activity of SV40 T antigen. Interestingly, a cellular DNA helicase was not inhibited by this compound, indicating that RK606 might be a specific inhibitor of T antigen helicase. To our knowledge, this is the first inhibitor besides ATP analogues for any DNA helicase.One of the repair inhibitors (RK679) was examined for its stability at different pH and for its extractability by several solvents. The behaviors of the repair inhibitor were similar to those of some kinds of tyrosine kinase inhibitors, genistein and daizein, therefore, we checked the effect of these tyrosine kinase inhibitors on cell-free NER assay. However, we could not find any effect of these compounds on NER,suggesting that RK679 is not either genistein or daizein but is rather different compound.
期刊论文(24)
专著(0)
科研奖励(0)
会议论文
van der Spek, P.J., Visser, C.E., Hanaoka, F., Smit, B., Hagemeijer, A., Bootsma, D., and Hoeijmakers, J.H.J.: "Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23.
van der Spek, P.J.、Visser, C.E.、Hanaoka, F.、Smit, B.、Hagemeijer, A.、Bootsma, D. 和 Hoeijmakers, J.H.J.:“小鼠同系物的克隆、比较作图和 RNA 表达
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Withers-Ward,E.S.et al.: "Human immunodeficiancy virus type 1 Vpr interacts with HHR23A,acellular protein implicated in nucloocide excision DNA repair" J.Virol.71. 9732-9742 (1997)
Withers-Ward,E.S.等人:“人类免疫缺陷病毒 1 型 Vpr 与 HHR23A 相互作用,HHR23A 是一种参与核苷酸切除 DNA 修复的非细胞蛋白”J.Virol.71。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Yokoi,M.et al.: "Molecular cloning of the cDNA for the catalytxc subunit of plane DNA polymarased and its celd-cycle dependent oxpression." Genes to Cells. 2. 695-710 (1997)
Yokoi,M.et al.:“平面 DNA 聚合酶催化亚基 cDNA 的分子克隆及其 celd 循环依赖性氧化作用。”
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
共 23 条
    Study on rapid and hypersensitive screening of chemical genotoxin using mammalian cells defective for DNA damage-response factors
    • 批准号:
      15K14953
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.41万
    • 财政年份:
      2015
    • 负责人:
      HANAOKA Fumio
    • 依托单位:
    Functional analyses and development of inhibitors based on higher-order structure of translesion DNA polymerase eta
    • 批准号:
      15H04646
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.82万
    • 财政年份:
      2015
    • 负责人:
      HANAOKA Fumio
    • 依托单位:
    Analyses of functional roles of TLS polymerases using transgenic mice
    • 批准号:
      22249005
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $31.2万
    • 财政年份:
      2010
    • 负责人:
      HANAOKA Fumio
    • 依托单位:
    Cellular responses to inhibition of DNA replication fork progression at DNA lesions
    海外基金