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Study of antiviral and anticancer effects of polyphenols

Study of antiviral and anticancer effects of polyphenols
多酚的抗病毒和抗癌作用研究
批准号:
15590238
负责人:
NAKASHIMA Hideki
金额:
$2.05万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004

项目摘要

项目成果

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中文摘要
翻译
1)抗病毒研究(1)抗HTV检测:用HIV-I感染MT-4细胞,并与不同浓度的受试化合物孵育。孵育5d后,用四甲基偶氮唑盐比色法测定细胞活力,以评价受试化合物对HIV诱导的CPE的抑制活性。(2)抗HSV实验:将HSV-1感染的Vero细胞与受试化合物共同孵育,以抑制病毒诱导的CPE活性为指标。2)细胞毒活性研究(1)细胞毒活性测定:3种口腔肿瘤细胞系(HSG、HSC-2、HSC-3)和3种正常细胞(HGF、HPC、HPLF)与受试化合物共同孵育。培养24小时后,用mtt法测定相对活细胞数。(2)dna片段化检测:用受试化合物…处理培养细胞用含逆转录病毒的mdr1/A基因转染小鼠T细胞淋巴瘤细胞株L5179,筛选出表达mdr1基因的细胞。通过对B16-BL6黑色素瘤细胞的实验性肺转移实验,研究了化合物的逆转活性。(4)用ESR波谱分析了Caspase的活性和抗自由基活性。(5)通过对B16-BL6黑色素瘤细胞的实验性肺转移实验,研究了几种植物的提取物对黑色素瘤的抑制作用。托波龙衍生物由于自由基介导的氧化还原反应而具有抗癌活性。4F-苯甲酰基-TE14011是合成肽T22和CXCR4拮抗剂的类似物,被一种可生物降解的聚合物聚D,L-乳酸包裹。皮下单次注射4F-苯甲酰基-TE14011-聚乳酸可显著减少B16-BL6黑色素瘤细胞肺转移形成的集落数量。较少
英文摘要
1)Antiviral study(1)Anti-HTV assay : MT-4 cells were infected with HIV-I and incubated in the presence of various concentrations of test compounds. After incubation for 5 days, cell viability was quantified by MTT assay to estimate a inhibition activity of test compounds against HIV induced CPE. Test compounds were alkyl-ologosaccharides, synthetic peptides, and an extract from, an Indian medical plant, Indigofera cordifora.(2)Anti-HSV assay : HSV-1 infected Vero cells were incubated in the presence of test compounds and antiviral activity was evaluated as the inhibition activity against virus induced CPE.2)Study for anticancer activities(1)Assay for cytotoxic activity : Three human oral tumor cell lines, (HSG, HSC-2, HSC-3), and 3 human normal cells, (HGF, HPC, HPLF) were incubated in the presence of test compounds. After 24 h incubation, the relative viable cell number was detenraned by MTT assay.(2)Assay for DNA fragmentation : DNA fragmentation from cultured cells with test compoun … More ds treatment was determined to estimate the inhibitory activity against apoptosis.(3)L5179 mouse T cell lymphoma cell line was transfected with MDR1/A containing retrovirus and MDR1 expressing cells were selected. The reversed activity of test compounds were studied.(4)Caspase activation and anti-radical activity using by ESR spectroscopy were also carried out.(5)Anti-melanoma metastatic activity was assessed using an experimental pulmonary metastasis assay of B16-BL6 melanoma cells.According to the results of these experiments, extracts from several plants, such as Anastasia Red, demonstrate anticancer activity and inhibition of MDR expression. Tropolone derivatives have anticancer activity due to radical mediated redox reaction. 4F-benzoyl-TE14011,an analog of synthetic peptide T22 and CXCR4 antagonist, was encapsulating with a biodegradable polymer, poly D, L-lactic acid (PLA). Subcutaneous single administration of 4F-benzoyl-TE14011-PLA significantly reduced the number of colonies formed by pulmonary metastasis of B16-BL6 melanoma cells. Less
期刊论文(99)
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会议论文
Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide-scahffolds.
通过环状四肽支架的结构调整鉴定新型低分子量 CXCR4 拮抗剂。
DOI: --
发表时间: 2005
期刊: J.Med.Chem. 48
影响因子: --
作者: [Tamamura, H., Araki, T., Ueda, S., Wang, Z., Oishi, S., Esaka, A., Trent, J.O., Nakashima, H., Yamamoto, N., Peiper, S.C., Otaka, A., Fujii, N.]
通讯作者: N.
Cytotoxic activity of Azulenequiiiones against human oral tumor cell lines.
Azulenequiiones 对人口腔肿瘤细胞系的细胞毒活性。
DOI: --
发表时间: 2005
期刊: Anticancer Res. 25
影响因子: --
作者: [Wakabayashi, H., Nishishiro, M., Arikawa, S., Hashimoto, K., Kikuchi, H., Nishikawa, H., Kurihara, T., Terakubo, S., Shoji, Y., Nakashima, H., Motohashi, N., Sakagami, H.]
通讯作者: H.
Tamamura, H., Hiramatsu, K., Nakashima, H., et al.: "Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives."Org.Biomol.Chem.. 1. 3656-3662 (2003)
Tamamura, H.、Hiramatsu, K.、Nakashima, H. 等人:“基于 T140 衍生物合成具有低细胞毒性和改善的生物稳定性的有效 CXCR4 抑制剂。”Org.Biomol.Chem.. 1. 3656-3662 (
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
DOI: 10.2174/1381612043453009
发表时间: 2004-02
期刊: Current pharmaceutical design
影响因子: 3.1
作者: [Y. Shoji;H. Nakashima]
通讯作者: Y. Shoji;H. Nakashima
共 36 条
    A empirical study of short-term interest rate around its lower bound
    • 批准号:
      21530298
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.33万
    • 财政年份:
      2009
    • 负责人:
      NAKASHIMA Hideki
    • 依托单位:
    Improvement of Microwave Discharge Ion Engine with Antenna for Uniform and High dense Plasma Generation
    • 批准号:
      16560691
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.3万
    • 财政年份:
      2004
    • 负责人:
      NAKASHIMA Hideki
    • 依托单位:
    Study for Growth Factors which Expressed in HHV8 Infected Cells and Oral Epithelial Cells
    海外基金