Targeting proapoptotic PKCdelta signaling in hepatocellular carcinoma

靶向肝细胞癌中的促凋亡 PKCdelta 信号传导

• 批准号: 7589301
• 负责人: CHING-SHIH CHEN
• 金额: $ 16.5万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-01-01 至 2010-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7589301
• 关键词: Address; Apoptosis; Biological Assay; Biological Markers; Cancer Etiology; Cause of Death; Cell Line; Cell Survival; Cells; Cessation of life; Classification; Clinical Management; Data; Defect; Development; Disease; Drug effect disorder; Environment; Evaluation; Exhibits; Fostering; Functional disorder; Genetic; Glutathione S-Transferase; Goals; Growth; Hepatitis C; Hepatocyte; Human; Immunosuppression; Immunosuppressive Agents; Incidence; Induction of Apoptosis; Investigation; Laboratories; Lead; Libraries; Life; Link; Malignant Epithelial Cell; Malignant Neoplasms; Modeling; Molecular Abnormality; Molecular Target; Neoplasm Metastasis; Oral; Outcome; Parents; Patient Selection; Patients; Pharmaceutical Chemistry; Pharmaceutical Preparations; Predisposition; Prevalence; Primary carcinoma of the liver cells; Protein Kinase C; Reactive Oxygen Species; Research; Resistance; Resources; Signal Transduction; Site; Subcutaneous Tissue; System; Systemic Therapy; Therapeutic; Therapeutic Agents; United States; Validation; Western Blotting; Xenograft Model; Xenograft procedure; base; cancer therapy; citrate carrier; clinically relevant; disorder control; improved; in vivo; intrahepatic; neoplastic cell; new therapeutic target; novel; novel strategies; novel therapeutics; public health relevance; response; scaffold; small molecule; stem; tumor; tumor growth; tumor xenograft

DESCRIPTION (provided by applicant): Hepatocellular carcinoma (HCC) is a leading cause of death worldwide, and is rapidly increasing in prevalence in the United States. Current systemic therapies for the large proportion of HCC patients with advanced, nonresectable disease have been largely unsuccessful; thus, a clear need exists to develop effective, life- prolonging therapeutic strategies for this disease. The PI's laboratory has devoted vital resources to developing novel oral, small-molecule agents that target the molecular and cellular defects in HCC cells that make the clinical management of this disease so challenging. In this project, we focus on the mechanistic investigation and structural optimization of a novel class of protein kinase C (PKC)d-targeted agents by using FTY720, an immunosuppressive agent, as a scaffold. This study stems from our mechanistic finding that FTY720 triggers apoptosis in HCC cells by facilitating the activation of ROS-PKCd signaling. The following aims constitute the foci of this investigation: (1) to conduct structural optimization of FTY720 and mechanistic validation of optimal derivatives; and (2) to assess the in vivo effect of structurally optimized (S)-FTY2 derivatives on suppressing HCC xenograft growth. In Aim 1, lead optimization of FTY720 is directed at separating the immunosuppressive activity of FTY720 from its effects on ROS-PKCd signaling. (S)-FTY2, which represents a lead compound in this regard, will then be structurally optimized using a bioassay-guided, two-tiered strategy involving cell survival assays and Western blotting to screen against a (S)-FTY2-based compound library to generate potent PKCd-targeted agents. In Aim 2, the in vivo efficacies of optimal derivatives in suppressing the growth of HCC tumors will be examined in both orthotopic and ectopic xenograft tumor models. We expect the proposed studies to yield data in support of our hypothesis that targeting ROS- PKCd signaling by small-molecule agents represents a therapeutically relevant approach to treat HCC, and ultimately lead to new approaches that will improve the treatment of HCC and increase the survival of HCC patients. PUBLIC HEALTH RELEVANCE:Hepatocellular carcinoma (HCC) is a leading cause of death worldwide, and is rapidly increasing in prevalence in the United States. Our overall research goal is to develop novel therapeutic agents that target the molecular and cellular defects in HCC cells that make the clinical management of this disease so challenging. We expect that this project will ultimately yield new drugs that will improve the treatment of HCC and increase the survival of HCC patients.

描述（由申请人提供）：肝细胞癌（HCC）是全球死亡的主要原因之一，在美国的患病率正在迅速上升。目前对大部分晚期不可切除的HCC患者的全身治疗在很大程度上是不成功的；因此，明确需要开发有效的、延长生命的治疗策略来治疗这种疾病。PI的实验室投入了重要的资源来开发新的口服小分子药物，这些药物针对HCC细胞中的分子和细胞缺陷，这些缺陷使这种疾病的临床管理变得如此具有挑战性。本课题以免疫抑制剂FTY720为支架，对一类新的蛋白激酶C (PKC)d靶向药物进行机理研究和结构优化。本研究源于我们的机制发现FTY720通过促进ROS-PKCd信号的激活而触发HCC细胞凋亡。本研究的重点是：(1)对FTY720进行结构优化，并对最优衍生物进行机理验证；(2)评估结构优化的(S)-FTY2衍生物在体内抑制肝癌异种移植物生长的作用。在Aim 1中，FTY720的先导优化旨在将FTY720的免疫抑制活性与其对ROS-PKCd信号传导的影响分离开来。(S)-FTY2是这方面的先导化合物，然后将使用生物测定指导的两层策略进行结构优化，包括细胞存活试验和Western blotting，以筛选基于(S)-FTY2的化合物文库，以产生有效的pkcd靶向药物。在Aim 2中，将在原位和异位异种移植肿瘤模型中检查最佳衍生物抑制HCC肿瘤生长的体内效果。我们期望所提出的研究能够得到支持我们假设的数据，即通过小分子药物靶向ROS- PKCd信号是治疗HCC的一种治疗相关方法，并最终导致改善HCC治疗和提高HCC患者生存率的新方法。公共卫生相关性：肝细胞癌（HCC）是世界范围内导致死亡的主要原因，并且在美国的患病率正在迅速上升。我们的总体研究目标是开发针对HCC细胞分子和细胞缺陷的新型治疗药物，这些缺陷使这种疾病的临床管理具有挑战性。我们期望这个项目最终会产生新的药物，改善HCC的治疗，提高HCC患者的生存率。