Proteosome Inhibition Therapy for Hematologic Malignancy
血液恶性肿瘤的蛋白酶体抑制疗法
基本信息
- 批准号:7840394
- 负责人:
- 金额:$ 13.4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2006
- 资助国家:美国
- 起止时间:2006-06-01 至 2011-05-31
- 项目状态:已结题
- 来源:
- 关键词:Acute Lymphocytic LeukemiaAdultAntineoplastic AgentsApoptosisApoptosis PromoterBiologyBortezomibCell LineChildhoodClinicalClinical TrialsCytarabineDataDexamethasoneDose-LimitingDoxorubicinDrug usageEffectivenessFDA approvedHematologic NeoplasmsHodgkin DiseaseIfosfamideIn VitroLaboratoriesLeukemic CellLifeLymphocyteMalignant NeoplasmsMaximum Tolerated DoseMediatingModelingMolecular ProfilingMultiple MyelomaPathway interactionsPatientsPhasePhase I Clinical TrialsPhase II Clinical TrialsProteasome InhibitionProteasome InhibitorReed-Sternberg CellsRefractoryRelapseSafetySamplingSolidSolid NeoplasmTestingToxic effectUbiquitinationVelcadeVincristineVinorelbineasparaginasebasechemosensitizing agentchemotherapeutic agentchemotherapycytotoxicexperiencegenetic regulatory proteinimprovedin vivoinhibitor/antagonistleukemialeukemia/lymphomalymphoblastmulticatalytic endopeptidase complexneoplastic cellnovelphase 1 studypre-clinicalprotein expressionresearch studytumor
项目摘要
DESCRIPTION (provided by applicant): Bortezomib (PS-341, VELCADE) is a proteasome inhibitor, one of a novel class of chemotherapeutic agents that has been FDA-approved for the treatment of multiple myeloma in adults and is being tested as a chemosensitizer in a variety of adult solid tumor and hematologic malignancies. We have preclinical evidence that bortezomib is a potent inducer of apoptosis in leukemic cells and is synergistic or additive with several standard chemotherapy drugs used in leukemia treatment. Based on this data, I am directing a phase I clinical trial of bortezomib in pediatric patients with relapsed/refractory leukemia. I propose to conduct correlative biology experiments with patient samples obtained from the current phase I and two proposed phase 2 trials to improve our understanding of the mechanism(s) of action of bortezomib in vivo. Specifically, I would like to examine the effects of bortezomib on the NF-KB pathway and explore the use of bortezomib as a chemosensitizing agent in acute lymphoblastic leukemia (ALL) and Hodgkin's lymphoma (HL). Many short-lived regulatory proteins, such the NF-KB inhibitor kB, are ubiquitinated and degraded by proteasome inhibition. There is substantial evidence that NF-KB is deregulated in leukemias and lymphomas. I hypothesize that bortezomib induces tumor cell apoptosis by inhibiting NF-KB activation. I will examine the effects of bortezomib on tumor cell apoptosis, NF-KB activation, and pretreatment protein expression profiles. Since there is evidence that bortezomib-induced apoptosis may occur through NF-KB-independent mechanisms, I will also examine other key regulatory proteins that are degraded by ubiquitination. The phase I studies will be used to further refine correlative biology studies for the proposed phase 2 clinical trials that will examine the effectiveness of bortezomib as a chemosensitizing agent in relapsed ALL and HL.
描述(由申请人提供):bortezomib(PS-341,Velcade)是一种蛋白酶体抑制剂,是一种新型的化学治疗剂之一,已通过FDA批准了用于治疗成人多发性骨髓瘤的多发性骨髓瘤,并且正在作为各种成人固体固体肿瘤和血液的化学效应进行测试,并正在接受化学效应。我们有临床前证明硼替佐米是白血病细胞凋亡的有效诱导剂,并且与白血病治疗中使用的几种标准化学疗法药物具有协同作用或添加剂。基于这些数据,我指挥了对复发/难治性白血病的儿科患者的硼替佐米的I期临床试验。我建议与从当前I期和两项拟议的2期试验获得的患者样品进行相关生物学实验,以提高我们对硼替佐米在体内作用机制的理解。具体而言,我想检查硼替佐米对NF-KB途径的影响,并探讨硼替佐米作为急性淋巴细胞白血病(ALL)和Hodggkin的淋巴瘤(HL)中的化学敏化剂的使用。许多短寿命的调节蛋白,例如NF-KB抑制剂KB,都被蛋白酶体抑制剂泛素化和降解。有大量证据表明,NF-KB在白血病和淋巴瘤中受到管制。 我假设硼替佐米通过抑制NF-KB激活来诱导肿瘤细胞凋亡。我将研究硼替佐米对肿瘤细胞凋亡,NF-KB激活和预处理蛋白表达谱的影响。由于有证据表明硼替佐米诱导的凋亡可能通过NF-KB独立的机制发生,因此我还将检查其他因泛素化降解的关键调节蛋白。第一阶段的研究将用于进一步完善拟议的2期临床试验的相关生物学研究,该研究将研究硼替佐米作为复发和HL的化学敏化剂的有效性。
项目成果
期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Analysis of NF-κB Pathway Proteins in Pediatric Hodgkin Lymphoma: Correlations with EBV Status and Clinical Outcome-A Children's Oncology Group Study.
小儿霍奇金淋巴瘤中 NF-κB 通路蛋白的分析:与 EBV 状态和临床结果的相关性 - 一项儿童肿瘤学小组研究。
- DOI:10.1155/2012/341629
- 发表时间:2012
- 期刊:
- 影响因子:0
- 作者:Horton,TerzahM;Sheehan,AndreaM;López-Terrada,Dolores;Hutchison,RobertE;Narendra,Sonia;Wu,Meng-Fen;Liu,Hao
- 通讯作者:Liu,Hao
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Terzah M Horton其他文献
Terzah M Horton的其他文献
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{{ truncateString('Terzah M Horton', 18)}}的其他基金
Identifying Cell Stress Proteins that Predict Clinical Response in Pediatric AML
鉴定可预测儿童 AML 临床反应的细胞应激蛋白
- 批准号:
8439807 - 财政年份:2013
- 资助金额:
$ 13.4万 - 项目类别:
Identifying Cell Stress Proteins that Predict Clinical Response in Pediatric AML
鉴定可预测儿童 AML 临床反应的细胞应激蛋白
- 批准号:
8613472 - 财政年份:2013
- 资助金额:
$ 13.4万 - 项目类别:
Identifying Cell Stress Proteins that Predict Clinical Response in Pediatric AML
鉴定可预测儿童 AML 临床反应的细胞应激蛋白
- 批准号:
8838738 - 财政年份:2013
- 资助金额:
$ 13.4万 - 项目类别:
Proteosome Inhibition Therapy for Hematologic Malignancy
血液恶性肿瘤的蛋白酶体抑制疗法
- 批准号:
7623964 - 财政年份:2006
- 资助金额:
$ 13.4万 - 项目类别:
Proteosome Inhibition Therapy for Hematologic Malignancy
血液恶性肿瘤的蛋白酶体抑制疗法
- 批准号:
7418956 - 财政年份:2006
- 资助金额:
$ 13.4万 - 项目类别:
Proteosome Inhibition Therapy for Hematologic Malignancy
血液恶性肿瘤的蛋白酶体抑制疗法
- 批准号:
7030593 - 财政年份:2006
- 资助金额:
$ 13.4万 - 项目类别:
MITOCHONDRIAL DNA MUTATIONS IN CARCINOGENESIS
致癌过程中的线粒体 DNA 突变
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3034782 - 财政年份:1993
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$ 13.4万 - 项目类别:
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