Targeting c-Src in Head and Neck Cancer

头颈癌中的靶向 c-Src

• 批准号: 8007341
• 负责人: FAYE JOHNSON
• 金额: $ 24.98万
• 依托单位: UNIVERSITY OF TX MD ANDERSON CAN CTR
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-01-01 至 2014-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8007341
• 关键词: Accounting; Affect; Apoptosis; Appearance; Attenuated; Biological Assay; CISH gene; Cell Death; Cell Survival; Cessation of life; Clinical Trials; Cytokine Inducible SH2-Containing Protein; DNA; Dasatinib; Deglutition; Development; Disease; Distant; Doctor of Philosophy; Down-Regulation; Face; Family; Family member; Feedback; Future; Goals; Growth Factor; Head and Neck Cancer; Head and Neck Squamous Cell Carcinoma; Head and neck structure; Human; Impairment; In Vitro; Incidence; Lead; Malignant Epithelial Cell; Malignant Neoplasms; Measures; Mediating; Modeling; Molecular; Molecular Target; Morbidity - disease rate; Mus; Neoplasm Metastasis; New Agents; Nodal; Nude Mice; Operative Surgical Procedures; Oral; Pathway interactions; Patients; Pharmaceutical Preparations; Phase; Phosphotransferases; Plasma; Protein Array; Protein Family; Protein Tyrosine Kinase; Proteins; RNA; Relative (related person); Resistance; Role; SRC gene; STAT3 gene; STAT5A gene; Sampling; Signal Pathway; Signal Transduction; Signal Transduction Pathway; Social isolation; Somatic Mutation; Specimen; Speech; Systemic Therapy; Testing; Therapeutic Agents; Therapeutic Effect; Therapeutic Studies; Tissues; Translating; Transplantation; Treatment Efficacy; Tumor Tissue; United States; Xenograft procedure; angiogenesis; cancer cell; cytotoxic; cytotoxicity; efficacy testing; improved; in vivo; inhibitor/antagonist; migration; mortality; mouse model; mouth squamous cell carcinoma; neoplastic cell; novel; protein expression; protein-tyrosine kinase c-src; public health relevance; response; src-Family Kinases; treatment effect; tumor

DESCRIPTION (provided by applicant): Targeting Src Kinases in Head and Neck Cancer Head and neck squamous cell carcinoma (HNSCC) are common worldwide and are particularly difficult to treat because both the tumor and the treatment can impair essential functions, such as speech and swallowing, and severely alter facial appearance. Local invasion is a critical determinant of both morbidity and mortality for HNSCC and is associated with worse locoregional control and decreased survival. There is a critical need to improve systemic therapy to treat both local invasion and distant metastatic disease. One promising molecular target in HNSCC for which new agents have been developed is c-Src. Inhibition of c-Src causes a significant and universal inhibition of migration and invasion of HNSCC cells; however, the cytotoxic effects of c-Src inhibition are less predictable. Defining mechanisms that limit the cytotoxic effects of c-Src inhibitors may result in an ideal combination of therapeutic agents for HNSCC that inhibits both local invasion and leads to significant cytotoxicity. As STATs can mediate proliferation and survival downstream of c-Src, we studied the role of STATs in modulating the effects of c-Src inhibition. We discovered a novel feedback pathway that leads to the reactivation of STAT3 via JAK which mediates resistance to c-Src inhibitors. We investigated feedback pathways leading to STAT3 activation and found that c-Src inhibition leads to down- regulation of suppressor of cytokine signaling 2 (SOCS2), a negative regulator of JAK/STAT3. Blockade of this feedback pathway significantly enhances the cytotoxic effect of c-Src inhibition. We hypothesize that sustained c-Src kinase inhibition leads to JAK/STAT3 reactivation via a novel feedback pathway involving SOCS2 and that inhibition of this feedback pathway will enhance the therapeutic efficacy of c-Src inhibition. We will test this hypothesis with three specific aims: To elucidate the mechanism underlying the feedback loop leading to STAT3 activation following sustained c-Src inhibition in HNSCC; to evaluate whether JAK inhibition enhances the therapeutic efficacy of the c-Src inhibitor dasatinib in an orthotopic model of HNSCC; and to develop and characterize a heterotransplant model of HNSCC in which to test biologic and signaling effects of c-Src and JAK inhibition. In the latter aim, we will evaluate the feedback pathway in a novel patient-derived heterotransplant model that could serve as a better surrogate for therapeutic studies in human HNSCC. Our long-term goal is to translate these findings into a future clinical trial in HNSCC patients that will test the efficacy of dual-targeting JAK and c-Src inhibition to improve treatment options for this deadly disease. PUBLIC HEALTH RELEVANCE: Cancers that occur in the head and neck region are common in the United States and often result in death or impairment of essential functions (e.g., speech and swallowing) or severely altered facial appearance. Thus, there is a great need to improve systemic therapy for patients with these tumors in order to increase cure rates and reduce morbidity. We have identified a family of proteins (Src family of non-receptor tyrosine kinases) that, when inhibited, can inhibit invasion and lead to cancer cell death. The goal of this proposal is to provide strategies to enhance the therapeutic effects of inhibition of the Src proteins in head and neck cancer.

描述(申请人提供)：靶向Src激酶治疗头颈部癌症头颈部鳞状细胞癌(HNSCC)在世界各地都很常见，尤其难以治疗，因为肿瘤和治疗都会损害基本功能，如言语和吞咽，并严重改变面部外观。局部侵袭是HNSCC发病率和死亡率的关键决定因素，并与较差的局部区域控制和降低存活率有关。目前迫切需要改进全身治疗，以治疗局部侵袭和远处转移疾病。在HNSCC中一个有希望的分子靶点是c-Src，已经为其开发了新的药物。抑制c-Src可以显著抑制HNSCC细胞的迁移和侵袭；然而，c-Src抑制的细胞毒作用是不可预测的。确定限制c-Src抑制剂细胞毒作用的机制可能导致HNSCC治疗药物的理想组合，既能抑制局部侵袭，又能导致显著的细胞毒性。由于STATS可以介导c-Src下游的增殖和存活，我们研究了STATs在调节c-Src抑制效应中的作用。我们发现了一条新的反馈途径，通过JAK介导对c-Src抑制剂的耐药性，从而导致STAT3的重新激活。我们研究了导致STAT3激活的反馈通路，发现c-Src抑制导致JAK/STAT3的负调控因子细胞因子信号转导抑制因子2(SOCS2)的下调。阻断这一反馈通路可显著增强c-Src抑制的细胞毒作用。我们假设，持续的c-Src激酶抑制导致JAK/STAT3通过涉及SOCS2的新的反馈通路重新激活，并且抑制该反馈通路将增强c-Src抑制的治疗效果。我们将通过三个具体的目标来验证这一假说：阐明在HNSCC中持续的c-Src抑制后反馈环导致STAT3激活的潜在机制；评估JAK抑制是否增强c-Src抑制剂达沙替尼在HNSCC原位模型中的治疗效果；以及建立和表征HNSCC的异种移植模型，在该模型中测试c-Src和JAK抑制的生物和信号效应。在后一个目标中，我们将评估一种新的患者来源的异种移植模型中的反馈途径，该模型可以为人类HNSCC的治疗研究提供更好的替代。我们的长期目标是将这些发现转化为未来在HNSCC患者中进行的临床试验，该试验将测试双靶向JAK和c-Src抑制的有效性，以改进这种致命疾病的治疗选择。 公共卫生相关性：发生在头部和颈部的癌症在美国很常见，通常会导致死亡或基本功能(如言语和吞咽)受损，或严重改变面部外观。因此，迫切需要改进对这些肿瘤患者的系统治疗，以提高治愈率和降低发病率。我们已经确定了一个蛋白质家族(非受体酪氨酸激酶的Src家族)，当被抑制时，可以抑制侵袭并导致癌细胞死亡。这项建议的目的是提供策略，以提高抑制Src蛋白在头颈部癌症中的治疗效果。