ROLE OF NOTCH-EGFR PATHWAY COOPERATIVITY IN BASAL-LIKE BREAST CANCER

NOTCH-EGFR 通路协同作用在基底样乳腺癌中的作用

• 批准号: 8191989
• 负责人: LOREN Scott MICHEL
• 金额: $ 19.84万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-01 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8191989
• 关键词: Address; Affect; Antibodies; Apoptosis; Biological Markers; Breast Cancer Cell; Cell Death; Cell Line; Cell Survival; Cells; Clinic; Clinical Trials; Clinical Trials Design; Data; Development; Disease; Dose; Epidermal Growth Factor Receptor; Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor; Family member; Foundations; Gene Dosage; Goals; Growth; Human; Immunodeficient Mouse; Individual; Investigation; Maintenance; Malignant Neoplasms; Mammary gland; Measurable; Measures; Mediating; Modification; Oncogene Proteins; Oncogenic; Pathway interactions; Patient Selection; Pharmaceutical Preparations; Play; Population; Process; RNA Interference; Reagent; Receptor Inhibition; Relapse; Relative (related person); Reporting; Research; Resistance; Role; Signal Transduction; Solid Neoplasm; Staging; Stem cells; Testing; Therapeutic; Toxic effect; Universities; Washington; Work; anticancer research; chemotherapy; cytotoxicity; design; gamma secretase; in vivo; inhibitor/antagonist; malignant breast neoplasm; new technology; new therapeutic target; notch protein; novel; prevent; receptor; receptor expression; receptor function; research study; restoration; therapeutic target; treatment strategy; triple-negative invasive breast carcinoma; tumor; tumor xenograft

DESCRIPTION (provided by applicant): Basal-like breast cancer (BLBC, or triple-negative) is a highly lethal form of the disease for which effective therapeutics are lacking. This lethality is thought to be due in part to the increased numbers of tumor- initiating (or stem) cells measured in BLBCs. The epidermal growth factor receptor (EGFR) is commonly expressed in these tumors, but inhibitors against the receptor have shown measurable but limited activity in breast cancer clinical trials. In contrast, EGFR is an effective target in multiple other solid tumor types. Even though clinical trials using EGFR inhibitors continue in breast cancer, the lack of efficacy of these agents in this disease remains poorly understood. BLBCs also show frequent hyperactivation of Notch receptors, which are oncogenic in the mammary gland. The four family members are commonly co-expressed in breast cancer cells where they can play opposing or redundant roles. Their activation is dependent on the enzymatic activity of the gamma secretase complex, inhibitors of which (GSIs) are being trialed in the clinic. These drugs globally inhibit all four receptors and can produce significant toxicity, motivating investigation into less toxic approaches to blocking Notch signaling. Fortunately, many Notch-dependent processes are sensitive to gene dosage and are receptor specific. Therefore, complete and pan-receptor inhibition may not be necessary for all therapeutic applications involving Notch receptors. We have recently reported a synthetic lethal relationship between the Notch and EGFR pathways (Dong, et al., Cancer Research, July 2010). Through the following aims, we will test the hypothesis that Notch and EGFR receptors function as cooperating oncoproteins required for BLBC cell survival. Specific Aim 1. To examine the effect of combined Notch-EGFR pathway inhibition on tumor-initiating cell survival in BLBC tumors. We will assess the relative ability of combined pathway inhibition to eradicate the tumor-initiating and more differentiated fractions of breast cancer cells. We will also begin to determine the efficacy of combined pathway inhibition against primary human BLBC tumors using a novel technology wherein these cancers are grafted into immunodeficient mice, and investigate the requirement for functional Notch-EGFR pathways in a broader panel of BLBC cell lines that show variable EGFR expression. Specific Aim 2. To determine the ability of partial Notch pathway inhibition to induce synthetic lethality when combined with EGFR blockade in BLBC cells. Partial pathway inhibition will be achieved through two strategies, dose modifications of GSI and receptor-specific knockdowns. In combination with EGFR blockade, we will examine the extent to which these approaches induce cell death and how they affect the viability of tumor-initiating and differentiated cells. Conversely, through forced expression of activated receptors, the ability of individual receptors to suppress cell death and expand the tumor-initiating population in the presence of GSI and EGFR inhibitor treatment will be measured. PUBLIC HEALTH RELEVANCE: The goal of this research is to lay the foundation for a clinical trial using Notch and EGFR inhibitors in basal-like breast cancer. Specifically, the results of this work will help direct the clinical trial design of combined Notch-EGFR inhibition towards early or late stage breast cancer. They also have the potential to facilitate patient selection through the identification of relevant biomarkers of sensitivity to combined pathway inhibition.

描述(申请人提供)：基底细胞样乳腺癌(BLBC，或三阴性)是一种高度致命的疾病形式，缺乏有效的治疗方法。这种致命性被认为部分是由于在BLBC中测量到的启动肿瘤(或干细胞)的细胞数量增加。表皮生长因子受体(EGFR)在这些肿瘤中普遍表达，但在乳腺癌临床试验中，针对该受体的抑制剂显示出可测量但有限的活性。相反，EGFR是多种其他实体肿瘤的有效靶点。尽管使用EGFR抑制剂治疗乳腺癌的临床试验仍在继续，但这些药物对这种疾病缺乏疗效的原因仍然知之甚少。BLBC还经常表现出Notch受体的过度激活，这种受体在乳腺中是致癌的。这四个家族成员通常在乳腺癌细胞中共同表达，在那里他们可以扮演相反或多余的角色。它们的激活依赖于伽马分泌酶复合体的酶活性，其抑制剂(GSI)正在临床试验中。这些药物在全球范围内抑制所有四种受体，并可能产生显著的毒性，促使人们研究毒性较低的方法来阻断Notch信号。幸运的是，许多依赖Notch的过程对基因剂量敏感，并且是受体特异性的。因此，对于所有涉及Notch受体的治疗应用，完全和泛受体抑制可能不是必需的。我们最近报道了Notch和EGFR通路之间的合成致死关系(董等人，癌症研究，2010年7月)。通过以下目标，我们将检验Notch和EGFR受体作为BLBC细胞生存所需的协同癌蛋白发挥作用的假设。具体目的1.检测联合抑制Notch-EGFR通路对BLBC肿瘤启动细胞存活的影响。我们将评估联合抑制途径的相对能力，以根除乳腺癌细胞的启动和分化程度较高的部分。我们还将开始使用一种新技术来确定联合途径抑制对原发人类BLBC肿瘤的有效性，其中这些癌症被移植到免疫缺陷小鼠体内，并研究在更广泛的BLBC细胞系中对功能Notch-EGFR途径的需求，这些细胞株表现出可变的EGFR表达。具体目的2.确定部分抑制Notch通路与EGFR阻断联合应用对BLBC细胞的合成致死性的影响。部分通路抑制将通过两种策略实现，GSI的剂量调整和受体特异性击倒。结合EGFR阻断，我们将检查这些方法诱导细胞死亡的程度，以及它们如何影响启动肿瘤和分化的细胞的活性。相反，通过强制表达激活的受体，将测量在GSI和EGFR抑制剂治疗的情况下，单个受体抑制细胞死亡和扩大肿瘤启动群体的能力。 公共卫生相关性：这项研究的目标是为使用Notch和EGFR抑制剂治疗基底细胞样乳腺癌的临床试验奠定基础。具体地说，这项工作的结果将有助于指导Notch-EGFR联合抑制早期或晚期乳腺癌的临床试验设计。它们还有可能通过识别对联合途径抑制敏感的相关生物标记物来促进患者选择。