Novel Antitumor Agents
Novel Antitumor Agents
批准号:
9265412
负责人:
KUO-HSIUNG LEE
金额:
$37.64万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-01 至 2019-04-30
关键词:
Antineoplastic AgentsBRCA1 geneBRCA2 geneBiological AssayBreast Cancer TreatmentBreast Cancer cell lineCaliforniaCancer EtiologyCancer-Predisposing GeneCell Cycle ArrestCellsChemicalsChemotherapy-Oncologic ProcedureChromatographyClinicalClinical TrialsCollaborationsCombinatorial Chemistry TechniquesCouplesDNA Sequence AlterationDevelopmentDiagnosisEvaluationFractionationGenetic EngineeringGoalsGonadal Steroid HormonesGrantHumanIn VitroInheritedKnockout MiceLaboratory ResearchLeadMedicinal PlantsMethodsModificationMolecularMolecular ModelsNational Cancer InstituteNatural ProductsNormal tissue morphologyPaperPathway interactionsPharmaceutical ChemistryPharmaceutical PreparationsPharmacologyPhosphotransferasesPhysical Chemical TechniquePlant ExtractsPlant SourcesPlantsPositioning AttributePredispositionProcessProductivityPublishingReceptor CellResearchRiskSignal Transduction PathwaySourceStructureStructure-Activity RelationshipTP53 geneTechniquesTherapeutic UsesTreatment-Related CancerTumor Cell LineTumor Suppressor GenesUniversitiesVascular PlantWomanXenograft procedureanalogantitumor agentbasecancer typeconditional mutantcytotoxicdrug candidateexperienceimprovedin vivoinnovationmalignant breast neoplasmmolecular modelingmouse modelmutantneotanshinlactonenovelnovel anticancer drugnovel therapeuticspre-clinicalpreclinical evaluationpreclinical studypreclinical trialprogramspublic health relevancerepositoryscreening
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The objective of the proposed research is to discover and develop new classes of anti-breast cancer agents from higher plants, which have been and still remain a significant source of new drugs. We will identify structurally unique hits from rare
sources of plants, particularly rainforest extracts with confirmed cytotoxic activity as screened b the National Cancer Institute, as well as medicinal plants used for cancer-related therapy. Lead compounds, optimized using medicinal chemistry approaches, will be subjected to critical preclinical in vivo assessment, not only with conventional xenograft mouse models, but also with an innovative and unique genetically engineered spontaneous breast cancer mouse model having conditional mutations on tumor suppressor genes Brca1 and p53. Furthermore, we will explore possible mechanism(s) of action based on chemical profiling and effects on responsible pathways, including sex steroid receptors, cell cycle arrest, kinase inhibition, or signal transduction pathways. The overall goals of our program are to identify and develop clinical trial candidates, especially for treating breast cancers. The following specific studies will be carried out to accomplish our goals. Specific Aim-1: In vitro screening and bioactivity-directed fractionation and isolation to identify breast cancer-selective compounds starting from plant extracts with confirmed activity and counter-screened in-house on the basis of susceptibility to breast cancer cell lines. Specific Aim-2: New lead optimization using synthetic modifications to improve pharmacological profile. Structural characterization of new active leads (Aim 1) and modified compounds (Aim 2) will be accomplished by chemical, physical, and spectroscopic techniques. Specific Aim-3: Two-step in vivo evaluations to confirm activity in mouse models, both conventional xenograft mouse models and innovative breast cancer Brca1/p53-Crec mouse model. Specific Aim-4: Mechanism of action studies to identify druggable targets and compounds for breast cancer treatment. Advantages of our program include 1) an excellent supply of highly active lead compounds and promising cytotoxic plant species, including rainforest species from the NCI Natural Product Repository Program, (2) excellent productivity in isolation and structural modification of new leads with new mechanisms of action as clinical trials candidates, which in turn could lead to innovative methods for cancer chemotherapy, and (3) superior prospects for the successful development of a clinically useful drug, based on promising in vivo results with neo-tanshinlactone analogs against breast cancers. An emphasis of our study will be on finding optimal analogs from these different compound classes to advance to anticancer clinical trials during the next grant period.
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DOI:
10.1021/jm5003588
发表时间:
2014-07-24
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Wang MJ, Liu YQ, Chang LC, Wang CY, Zhao YL, Zhao XB, Qian K, Nan X, Yang L, Yang XM, Hung HY, Yang JS, Kuo DH, Goto M, Morris-Natschke SL, Pan SL, Teng CM, Kuo SC, Wu TS, Wu YC, Lee KH]
通讯作者:
Lee KH
Spiro[3.5]nonenyl Meroterpenoid Lactones, Cryptolaevilactones G-L, an Ionone Derivative, and Total Synthesis of Cryptolaevilactone M from Cryptocarya laevigata.
Spiro [3.5]非烯基MOROTERPENOID内膜酮,加密陶式乳酸酮G-L,一种离子酮衍生物和来自加密氏菌Laevigata的加密氏素M的总合成。
DOI:
10.1021/acs.jnatprod.8b00732
发表时间:
2019-09-27
期刊:
Journal of natural products
影响因子:
5.1
作者:
[Tsurumi F, Miura Y, Nakano M, Saito Y, Fukuyoshi S, Miyake K, Newman DJ, O'Keefe BR, Lee KH, Nakagawa-Goto K]
通讯作者:
Nakagawa-Goto K
DOI:
10.1021/jm401686b
发表时间:
2014-02-13
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Chen CY, Yang SC, Lee KH, Yang X, Wei LY, Chow LP, Wang TC, Hong TM, Lin JC, Kuan C, Yang PC]
通讯作者:
Yang PC
DOI:
10.1016/j.bmc.2013.11.035
发表时间:
2014-01-01
期刊:
Bioorganic & medicinal chemistry
影响因子:
3.5
作者:
[Zhang ZJ, Tian J, Wang LT, Wang MJ, Nan X, Yang L, Liu YQ, Morris-Natschke SL, Lee KH]
通讯作者:
Lee KH
DOI:
10.1016/j.bmcl.2013.06.083
发表时间:
2013-09-15
期刊:
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
影响因子:
2.7
作者:
[Cheng, Yung-Yi, Liu, Chin-Yu, Tsai, Meng-Tung, Lin, Hui-Yi, Yang, Jai-Sing, Wu, Tian-Shung, Kuo, Sheng-Chu, Huang, Li-Jiau, Lee, Kuo-Hsiung]
通讯作者:
Lee, Kuo-Hsiung
共 65 条
Novel Antitumor Agents
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批准号:8685206
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项目类别:
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资助金额:$36.51万
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财政年份:2013
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负责人:KUO-HSIUNG LEE
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依托单位:
Novel Antitumor Agents
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批准号:8550474
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项目类别:
-
资助金额:$37.64万
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财政年份:2013
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负责人:KUO-HSIUNG LEE
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依托单位:
Novel Antitumor Agents
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批准号:8843732
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项目类别:
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资助金额:$37.64万
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财政年份:2013
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:7917025
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项目类别:
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资助金额:$11.33万
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财政年份:2009
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:7740179
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项目类别:
-
资助金额:$45.68万
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财政年份:2007
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:7995208
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项目类别:
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资助金额:$45.15万
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财政年份:2007
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:7418742
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项目类别:
-
资助金额:$46.43万
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财政年份:2007
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:8196844
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项目类别:
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资助金额:$45.05万
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财政年份:2007
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负责人:KUO-HSIUNG LEE
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依托单位:
Modified Triterpines as Potent HIV Fusion Inhibitors
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批准号:7535010
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项目类别:
-
资助金额:$44.82万
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财政年份:2007
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负责人:KUO-HSIUNG LEE
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依托单位:
CHEMICAL DIVERSITY LIBRARIES FROM MEDICINAL PLANTS (RMI)
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批准号:7274185
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项目类别:
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资助金额:$39.22万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
CHEMICAL DIVERSITY LIBRARIES FROM MEDICINAL PLANTS
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批准号:7125591
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项目类别:
-
资助金额:$39.36万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
CHEMICAL DIVERSITY LIBRARIES FROM MEDICINAL PLANTS (RMI)
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批准号:7018956
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项目类别:
-
资助金额:$48.32万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTITUMOR AGENTS
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批准号:7614398
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项目类别:
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资助金额:$31.22万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTITUMOR AGENTS
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批准号:7076964
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项目类别:
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资助金额:$30.19万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTITUMOR AGENTS
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批准号:7407360
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项目类别:
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资助金额:$30.37万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTITUMOR AGENTS
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批准号:6965604
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项目类别:
-
资助金额:$33.45万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTITUMOR AGENTS
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批准号:7282435
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项目类别:
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资助金额:$30.13万
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财政年份:2005
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTI-HIV AGENTS
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批准号:6373285
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项目类别:
-
资助金额:$36.65万
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财政年份:1992
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTI-HIV AGENTS
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批准号:6146772
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项目类别:
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资助金额:$39.6万
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财政年份:1992
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负责人:KUO-HSIUNG LEE
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依托单位:
PLANT ANTI-HIV AGENTS
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批准号:6631939
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项目类别:
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资助金额:$38.88万
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财政年份:1992
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负责人:KUO-HSIUNG LEE
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依托单位:
海外基金