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MOLECULAR ONCOLOGY PROGRAM PROJECT

MOLECULAR ONCOLOGY PROGRAM PROJECT
分子肿瘤学计划项目
批准号:
6743654
负责人:
Richard Jove
金额:
$120.29万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-05-01 至 2006-04-30

项目摘要

项目成果

Richard Jove的其他基金

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中文摘要
翻译
分子肿瘤学项目(MOPP)的最终目标是在更好地了解肿瘤细胞存活和耐药性的机制的基础上,开发更有效的人类癌症治疗方法。这一目标将通过将分子机制的原始实验室研究与创新临床试验紧密结合来实现。为了实现这一目标,基础科学家和临床研究人员之间的合作是每个研究项目不可或缺的一部分:MOPP包括三个组成部分的研究项目、三个核心和九个临床方案。所有的研究项目都将以骨髓瘤为范例,或模型,来研究肿瘤细胞存活和治疗反应的机制。在这个模型中所做的观察也将扩展到其他癌症,包括乳腺癌和卵巢癌。项目一将研究肿瘤微环境通过赋予细胞粘附介导的耐药性来影响药物反应的假设。黏附的骨髓瘤细胞系改善化疗药物和放疗的治疗反应。项目二:通过调节细胞凋亡机制促进恶性进展,同时诱导化疗耐药。这一假设将在骨髓瘤研究和新辅助化疗的乳腺癌拓扑异构酶I和II的改变的II期临床试验中进行评估,拓扑异构酶I和II参与了对这些酶抑制剂的耐药性。实验室研究骨髓瘤,AML, NHL和CLL,以及某些实体瘤。组成项目的研究将由三个核心提供支持,包括行政核心、病理核心和临床试验核心。MOPP研究项目将通过这些密切结合的癌症治疗实验室和临床研究的高度协作性质得到显著加强。这些研究结果将为肿瘤细胞杀伤和耐药的分子机制提供新的见解,将直接转化为更有效的癌症治疗方法。
英文摘要
The ultimate goal of the Molecular Oncology Program Project (MOPP) is to develop more effective therapies for human cancer based on a better mechanistic understanding of tumor cell survival and drug resistance. The goal will be pursued through close integration of original laboratory studies on molecular mechanisms with innovative clinical trials. To achieve this goal, collaborations between basic scientists and clinical investigators are integral to each research project: MOPP comprises three component research project, three cores, and nine clinical protocols. All the research projects will use myeloma as a paradigm, or model, to study mechanisms of tumor cell survival and treatment response. Observations made in this model will also be extended to other cancers, including breast and ovarian cancer. Project I will investigate the hypothesis that the tumor microenvironment influences drug response by conferring cell adhesion-mediated drug resistance. Myeloma cell lines by adhesion improves treatment response to chemotherapy drugs and radiation. Project II malignant progression through regulation of apoptotic mechanisms that also induce resistance to chemotherapy. This hypothesis will be evaluated in myeloma studies and a phase II clinical trial of neoadjuvant chemotherapy in breast alterations of topoisomerases I and II are involved in drug resistance to inhibitors of these enzymes. Laboratory studies myeloma, AML, NHL, and CLL, as well as certain solid tumors. Research in the component projects will be supported by three cores, including the Administrative Core, the Pathology Core, and the Clinical Trials Core. The MOPP research projects will e significantly enhanced by the highly collaborative nature of these closely integrated laboratory and clinical studies of cancer therapeutics. Results of these studies will provide new insights into the molecular mechanisms of tumor cell killing and drug resistance that will be directly translated into more effective cancer therapies.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1158/0008-5472.can-09-0484
发表时间: 2009-09-01
期刊: Cancer research
影响因子: 11.2
作者: [Turner JG, Marchion DC, Dawson JL, Emmons MF, Hazlehurst LA, Washausen P, Sullivan DM]
通讯作者: Sullivan DM
Sequential intraperitoneal topotecan and oral etoposide chemotherapy in recurrent platinum-resistant ovarian carcinoma: results of a phase II trial.
序贯腹腔内拓扑替康和口服依托泊苷化疗治疗复发性铂耐药卵巢癌:II 期试验结果。
DOI: 10.1158/1078-0432.ccr-04-0574
发表时间: 2004
期刊: Clinical cancer research : an official journal of the American Association for Cancer Research.
影响因子: --
作者: [Sood,AnilK, Lush,Richard, Geisler,JohnP, Shahin,MarkS, Sanders,Linda, Sullivan,Dan, Buller,RichardE, Sorosky,JoelI]
通讯作者: Sorosky,JoelI
Sequential oral 9-nitrocamptothecin and etoposide: a pharmacodynamic- and pharmacokinetic-based phase I trial.
序贯口服 9-硝基喜树碱和依托泊苷:一项基于药效学和药代动力学的 I 期试验。
DOI: 10.1158/1535-7163.mct-06-0034
发表时间: 2006
期刊: Molecular cancer therapeutics
影响因子: 5.7
作者: [Simon,GeorgeR, Lush,RichardM, Gump,Jana, Tetteh,Leticia, Williams,Charles, Cantor,Alan, Antonia,Scott, Garrett,Christopher, Rocha-Lima,Caio, Fishman,Mayer, Sullivan,DanielM, Munster,PamelaN]
通讯作者: Munster,PamelaN
Inhibitors in Src Signaling for Antitumor Therapy
Inhibitors in Src Signaling for Antitumor Therapy
Inhibitors in Src Signaling for Antitumor Therapy
Inhibitors in Src Signaling for Antitumor Therapy
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