The pathophysiological role of nuclear EGFR in TNBC

核EGFR在TNBC中的病理生理作用

• 批准号: 9024152
• 负责人: DERIC L WHEELER
• 金额: $ 34.61万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-03-01 至 2021-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9024152
• 关键词: Affect; Amino Acids; Antibodies; Binding; Biological Models; Biology; Biopsy; Bladder; Breast Cancer Cell; Breast Cancer Patient; Breast Cancer cell line; C-terminal; Cell Nucleus; Cell membrane; Cell surface; Cetuximab; Clinic; Clinical; Clinical Trials; DNA Repair; DNA biosynthesis; Dasatinib; Data; Diagnostic; Disease; ERBB2 gene; Epidermal Growth Factor Receptor; Estrogens; Etiology; Genetic Transcription; Head and Neck Squamous Cell Carcinoma; Human; Knowledge; Laboratories; Lead; Left; Lung; Malignant Neoplasms; Maps; Measures; Mediating; Membrane; Membrane Protein Traffic; Modeling; Molecular Target; Mus; Newly Diagnosed; Nuclear; Nuclear Translocation; Oncogenes; Oncologist; Operative Surgical Procedures; Outcome; Pathologist; Pathway interactions; Patient-Focused Outcomes; Patients; Prevention; Progesterone; Protein Tyrosine Kinase; Publishing; Receptor Signaling; Research; Resected; Resistance; Role; Sampling; Series; Signal Pathway; Signal Transduction; Surgeon; Survival Rate; Testing; Therapeutic; Time; Translating; Translations; Tyrosine; United States; Variant; Woman; Work; Xenograft Model; Xenograft procedure; breast cancer diagnosis; cancer clinical trial; cancer subtypes; efficacy testing; in vivo; in vivo Model; kinase inhibitor; malignant breast neoplasm; novel; novel therapeutics; outcome forecast; overexpression; public health relevance; receptor; receptor expression; receptor function; resistance mechanism; response; src-Family Kinases; therapeutic target; trafficking; transcription factor; treatment response; triple-negative invasive breast carcinoma; tumor; tumor growth; tumor progression; tumor xenograft

 DESCRIPTION (provided by applicant): The objectives of this proposal are to determine 1) if the nuclear epidermal growth factor receptor (nEGFR) drives resistance to cetuximab in triple-negative breast cancer (TNBC) via its co-transcriptional functions, 2) if targeting nEGFR, by inhibiting its nuclear translocation, can increase the efficacy of cetuximab in TNBC and 3) if we can functionally target nEGFR in TNBC patients. Triple-negative breast cancer (TNBC) is a tumor that lacks estrogen, progesterone and HER2 receptors, leaving minimal therapeutic options. As a result, the prognosis of patients with TNBC remains poor. Recent studies revealed that approximately 50% of TNBC overexpress the oncogene EGFR, which predicts poor patient outcome in TNBC. Unfortunately, clinical trials testing the efficacy of the anti-EGFR monoclonal antibody cetuximab revealed little impact on outcomes in TNBC. This suggests a gap in our knowledge of how EGFR drives TNBC and how to target EGFR effectively in this disease. It is well established that EGFR functions in two distinct signaling compartments: 1) Classical membrane bound signaling and 2) nuclear signaling. Within the nucleus, EGFR performs two functions: 1) as a co-transcription factor enhancing transcription of cancer-promoting genes, and 2) as a tyrosine kinase responsible for phosphorylating substrates that enhance DNA replication and repair. We have published data showing that nuclear EGFR (nEGFR) confers resistance to cetuximab therapy and that the Src Family Kinases (SFKs) are necessary for nuclear translocation of the EGFR. In this proposal we hypothesize that nEGFR contributes to cetuximab resistance via its role as a nuclear co-transcription factor and serves as a functional molecular target in TNBC. To test this hypothesis we have mapped the EGFR C-terminal domain to identify key amino acids necessary for transcriptional activity of the EGFR. This resulted in an EGFR variant that lacks transcriptional activity but retains its signaling capacity that will be used to elucidate nEGFR transcriptional function in cetuximab resistance (Specific Aim 1). This proposal will further assess the therapeutic benefit of targeting both the classical and nEGFR signaling pathways simultaneously by abrogating nuclear translocation via SFK blockade (dasatinib) - followed by subsequent targeting of the classical EGFR signaling pathway with cetuximab in both orthotopic and patient derived xenograft model systems (Specific Aim 2). Finally, we will perform a window trial in nEGFR positive TNBC patients, to determine if we can target nEGFR in humans and redistribute EGFR expression to the plasma membrane where it can be inhibited by cetuximab therapy (Specific Aim 3). Collectively, these studies have potential to re-define how we target EGFR in TNBC and other nEGFR expressing cancers (HNSCC, Lung, bladder), by targeting both compartments of EGFR signaling, and thus turning a tumor that is intrinsically resistant to cetuximab into a tumor that is now sensitive to cetuximab. This investigative strategy can be readily translated to the clinic for treatment of TNBC patients.

 描述（由申请方提供）：本提案的目的是确定1）核表皮生长因子受体（nEGFR）是否通过其共转录功能驱动三阴性乳腺癌（TNBC）对西妥昔单抗的耐药性，2）靶向nEGFR是否可以通过抑制其核易位来增加西妥昔单抗在TNBC中的疗效，以及3）我们是否可以在TNBC患者中功能性靶向nEGFR。 三阴性乳腺癌（TNBC）是一种缺乏雌激素，孕激素和HER 2受体的肿瘤，留下最少的治疗选择。因此，TNBC患者的预后仍然很差。最近的研究表明，大约50%的TNBC过表达癌基因EGFR，这预示着TNBC患者的预后不良。不幸的是，测试抗EGFR单克隆抗体西妥昔单抗的疗效的临床试验显示对TNBC的结果几乎没有影响。这表明我们对EGFR如何驱动TNBC以及如何在这种疾病中有效靶向EGFR的知识存在差距。已经确定EGFR在两个不同的信号传导区室中起作用：1）经典的膜结合信号传导和2）核信号传导。在细胞核内，EGFR执行两种功能：1）作为共转录因子，增强促癌基因的转录，和2）作为酪氨酸激酶，负责磷酸化增强DNA复制和修复的底物。我们已经发表的数据显示，核EGFR（nEGFR）赋予西妥昔单抗治疗的抗性，并且Src家族激酶（SFK）是EGFR核易位所必需的。在该提案中，我们假设nEGFR通过其作为核共转录因子的作用促进西妥昔单抗耐药，并作为TNBC中的功能性分子靶点。为了验证这一假设，我们绘制了EGFR C-末端结构域，以确定EGFR转录活性所需的关键氨基酸。这导致EGFR变体缺乏转录活性但保留其信号传导能力，其将用于阐明西妥昔单抗耐药中的nEGFR转录功能（特定目的1）。该提案将进一步评估通过SFK阻断（达沙替尼）消除核转位同时靶向经典和nEGFR信号传导途径的治疗获益-随后在原位和患者来源的异种移植模型系统中使用西妥昔单抗靶向经典EGFR信号传导途径（具体目标2）。最后，我们将在nEGFR阳性的TNBC患者中进行一项窗口试验，以确定我们是否可以靶向人类的nEGFR并将EGFR表达重新分布到质膜，在那里它可以被西妥昔单抗治疗抑制（具体目标3）。总的来说，这些研究有可能重新定义我们如何在TNBC和其他表达nEGFR的癌症（HNSCC，肺，膀胱）中靶向EGFR，通过靶向EGFR信号传导的两个区室，从而将对西妥昔单抗具有内在耐药性的肿瘤转变为现在对西妥昔单抗敏感的肿瘤。这种研究策略可以很容易地转化为临床治疗TNBC患者。