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Signal Transduction in the Heart after Cancer Therapy

癌症治疗后心脏的信号转导

基本信息

批准号：
8067782
负责人：
KATHLEEN Louise GABRIELSON
金额：
$ 41万
依托单位：
JOHNS HOPKINS UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-08-01 至 2013-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8067782
关键词：
17-(Allylamino)-17-demethoxygeldanamycin Address Affect Animals Antibodies Antineoplastic Agents Binding Cancer Patient Cardiac Cardiac Myocytes Cardiomyopathies Cardiotoxicity Cell Culture Techniques Cell Death Cells Cessation of life Clinical Complication Consensus Sequence Data Diabetes Mellitus Doxorubicin Free Radical Scavengers Functional disorder Genetic Transcription Glutathione Goals HSP 90 inhibition Health Heart Heart failure Heat-Shock Proteins 90 Hydrogen Peroxide In Vitro Injury Laboratories Ligands Link Malignant Neoplasms Messenger RNA Mitochondria Modeling Molecular Molecular Chaperones Mus Neuregulins Oxidation-Reduction Oxidative Stress Pathway interactions Patients Pharmaceutical Preparations Proteins Public Health Publishing Rattus Resveratrol Risk Roche brand of trastuzumab Role Signal Transduction Small Interfering RNA Streptozocin Stress Testing Therapeutic Therapeutic Agents Toxic effect Transgenic Mice Transgenic Organisms Trastuzumab Xanthine Oxidase Xanthines Xenograft procedure base cancer cell cancer therapy effective therapy geranylgeranylacetone heart cell heart function in vivo inhibitor/antagonist lapatinib malignant breast neoplasm mitochondrial dysfunction mouse model novel strategies prevent promoter protein expression protein function small molecule treatment strategy

项目摘要

DESCRIPTION (provided by applicant): The new approach of targeted cancer therapy has been received well, but an underlying theme needs to be addressed. Many of the proteins that are targeted for cancer therapy also have a major role in the heart. Our laboratory's long-term goals are to better understand erbB2 and HSP90 function in the heart, identify patients at risk for cardiac injury from cancer therapy, and develop new treatment strategies that can effectively treat cancer while also protecting the heart from the cancer therapeutic agents. We hypothesize that erbB2 is induced in the heart by oxidative stress, and that it also has a central role in protecting the heart from oxidative stress (including stress induced by doxorubicin therapy). Furthermore, we hypothesize that the chaperone HSP90 cooperates in this cellular protection by stabilizing the erbB2 protein in heart cells. Aim 1: Determine the role of oxidative stress and associated cell signaling to induce cardioprotection through erbB2 or HSP90 (protein or mRNA) and the role of NF-:2 using the following oxidative stress models: 1) H2O2, xanthine/xanthine oxidase and glutathione depletion in rat cardiomyocytes and in vivo glutathione depletion 2) diabetes cardiomyopathy, and 3) redox modulation with resveratrol or geranylgeranylacetone to prevent doxorubicin toxicity. Additionally, we will determine the role of free radical scavengers on erbB2 expression and the role of erbB2 pathway inhibition on cellular protection during oxidative stress. Aim 2: Determine whether the cardioprotective role of erbB2 is due to a reduction of cardiac oxidative stress. Here we aim to assess whether: 1) erbB2 pathway inhibition in cardiomyocytes (through anti-erbB2 or siRNA) results in increased oxidative stress and dysfunction in the mitochondria, and thus increased sensitivity to doxorubicin, 2) lapatinib induces cardiac oxidative stress and cell death in vivo, with or without doxorubicin therapy compared to cancer xenografts, 3) transgenic cardiac-specific over-expression of erbB2 protects from oxidative stress and mitochondrial dysfunction in two models of oxidative stress (doxorubicin-induced cardiomyopathy and streptozotocin-induced diabetes cardiomyopathy). Aim 3: Determine the cellular protective role of HSP90 as a chaperone of erbB2 protein in the heart. Here we aim to assess whether: 1) cardiac-specific over-expression of HSP90 in a transgenic mouse model reduces heart failure, cell death and oxidative stress via stabilization of erbB2 in two models: doxorubicin-induced heart toxicity or streptozotocin-induced diabetes cardiomyopathy; 2) inhibiting HSP90 protein expression or function increases cardiomyocyte death during doxorubicin therapy in vitro with siRNA or in vivo with 17AAG in mice with cancer xenografts, and 3) HSP90 inhibitor (17AAG) affects cardiac erbB2 levels in isolated hearts and inhibits heart function and mitochondrial function. PUBLIC HEALTH RELEVANCE: The public health significance of this project is that we aim to protect patients from severe cardiotoxic effects of anti-cancer drugs, which in many cases, limits the use of otherwise effective therapies. The public health significance of this project is that we aim to protect patients from severe cardiotoxic effects of anti-cancer drugs, which in many cases, limits the use of otherwise effective therapies.

描述（由申请人提供）：靶向癌症治疗的新方法已经得到了很好的接受，但需要解决一个潜在的主题。许多针对癌症治疗的蛋白质也在心脏中发挥重要作用。我们实验室的长期目标是更好地了解erbB 2和HSP 90在心脏中的功能，识别癌症治疗中心脏损伤风险的患者，并开发新的治疗策略，可以有效治疗癌症，同时保护心脏免受癌症治疗药物的影响。我们假设erbB 2在心脏中由氧化应激诱导，并且它在保护心脏免受氧化应激（包括多柔比星治疗诱导的应激）方面也具有核心作用。此外，我们假设伴侣HSP 90通过稳定心脏细胞中的erbB 2蛋白在这种细胞保护中起作用。目标1：使用以下氧化应激模型确定氧化应激和相关细胞信号传导通过erbB 2或HSP 90（蛋白质或mRNA）诱导心脏保护的作用以及NF-：2的作用：1）大鼠心肌细胞中的H2 O2、黄嘌呤/黄嘌呤氧化酶和谷胱甘肽耗竭以及体内谷胱甘肽耗竭2）糖尿病心肌病，以及3）用白藜芦醇或香叶基香叶基丙酮进行氧化还原调节以防止多柔比星毒性。此外，我们还将确定自由基清除剂对erbB 2表达的作用以及erbB 2通路抑制对氧化应激过程中细胞保护的作用。目的2：确定erbB 2的心脏保护作用是否是由于心脏氧化应激的减少。在此，我们旨在评估：1）心肌细胞中的erbB 2途径抑制（通过抗erbB 2或siRNA）导致线粒体中氧化应激和功能障碍增加，从而增加对阿霉素的敏感性，2）拉帕替尼在体内诱导心脏氧化应激和细胞死亡，与癌症异种移植物相比，有或没有阿霉素治疗，3）在两种氧化应激模型（多柔比星诱导的心肌病和链脲佐菌素诱导的糖尿病心肌病）中，erbB 2的转基因心脏特异性过表达保护氧化应激和线粒体功能障碍。目的3：探讨热休克蛋白90作为erbB 2蛋白伴侣对心肌细胞的保护作用。本研究旨在评估：1）在转基因小鼠模型中心脏特异性过表达HSP 90是否通过稳定erbB 2来减少两种模型中的心力衰竭、细胞死亡和氧化应激：阿霉素诱导的心脏毒性或链脲佐菌素诱导的糖尿病心肌病;（二）在体外用siRNA或体内用17 AAG进行阿霉素治疗期间，抑制HSP 90蛋白表达或功能增加心肌细胞死亡。HSP 90抑制剂（17 AAG）影响离体心脏中的心脏erbB 2水平并抑制心脏功能和线粒体功能。公共卫生关系：该项目的公共卫生意义在于，我们的目标是保护患者免受抗癌药物的严重心脏毒性影响，在许多情况下，这限制了其他有效疗法的使用。该项目的公共卫生意义在于，我们的目标是保护患者免受抗癌药物的严重心脏毒性影响，在许多情况下，这限制了其他有效疗法的使用。