Signaling in the ovarian cancer metastatic microenvironment

卵巢癌转移微环境中的信号传导

• 批准号: 7987744
• 负责人: Jill Slack-Davis
• 金额: $ 31.37万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7987744
• 关键词: Accounting; Address; Animal Model; Arrestins; Arthritis; Asthma; Atherosclerosis; Autoimmunity; Cancer Etiology; Cancer Patient; Cell Communication; Cell Culture System; Cell Line; Cells; Cessation of life; Chi-Square Tests; Chronic; Clinical; Colitis; Cox Proportional Hazards Models; Data; Development; Diagnosis; Diagnostic Neoplasm Staging; Disease; Disease Progression; Disease Resistance; Disseminated Malignant Neoplasm; Exposure to; Flow Cytometry; Genetic Transcription; Goals; Greater sac of peritoneum; Incidence; Integrins; Invaded; Lead; Ligands; Lipids; Lysophosphatidic Acid Receptors; Lysophospholipids; Malignant neoplasm of ovary; Mediating; Mesothelial Cell; Mesothelium; Modeling; Molecular; Multiple Sclerosis; Mus; Natural Immunity; Neoplasm Metastasis; Ovarian Carcinoma; Pathway interactions; Patients; Peritoneal; Phospholipids; Phosphoric Monoester Hydrolases; Platinum; Play; Production; Recurrence; Refractory; Regulation; Reporting; Reverse Transcriptase Polymerase Chain Reaction; Role; Signal Pathway; Signal Transduction; Small Interfering RNA; Solid Neoplasm; Staging; Stimulus; Testing; Therapeutic Intervention; Time; Tumor Burden; Tumor Debulking; Tumor stage; Vascular Cell Adhesion Molecule-1; Woman; Xenograft Model; adaptive immunity; cancer cell; chemotherapy; defined contribution; design; effective therapy; improved; insight; lysophosphatidic acid; macrophage; metastatic process; mortality; mouse model; neoplastic cell; novel; outcome forecast; public health relevance; receptor; therapeutic target; tumor; tumor progression

DESCRIPTION (provided by applicant): Ovarian cancer is the fourth leading cause of cancer-related death among women. The relatively poor prognosis for ovarian cancer reflects the high incidence of metastasis at diagnosis. Indeed, 75% of patients are diagnosed with metastatic disease, which has a 5-year survival of 20-25%. The high mortality rate is due in large part to the lack of effective treatment options for metastatic cancer. Identifying the mechanisms that regulate ovarian cancer metastasis will provide much needed additional therapeutic targets for the treatment of ovarian cancer. We hypothesize that the integrin mediated interaction between the tumor cells and mesothelium is an important component of ovarian cancer progression. Ovarian carcinomas metastasize by invading through the mesothelium, a layer of mesothelial cells that line the peritoneal cavity. We reported a novel mechanism for the regulation of mesothelial invasion. Our data demonstrate that VCAM-1, which is expressed preferentially on the mesothelium of ovarian cancer patients, functions together with its ligand, a4¿1 integrin (expressed on ovarian cancer cells), to promote mesothelial invasion in cell culture systems. Importantly, inhibition of VCAM-1 function increased survival and decreased tumor burden in a mouse model of ovarian cancer peritoneal metastasis. Our preliminary data demonstrate that lysophosphatidic acid (LPA), a bioactive phospholipid found in abundance in the peritoneal cavity of ovarian cancer patients, regulates mesothelial invasion and mesothelial VCAM-1 expression. Importantly, chronic production of LPA by mesothelial cells results in constitutive VCAM-1 expression that is refractory to other stimuli, including TNF-a, a well- characterized regulator of VCAM-1 expression. The goal of this proposal is to determine the mechanisms that regulate VCAM-1 expression on the mesothelium of ovarian cancer patients. This will be accomplished with the following specific aims: 1) determine the signaling pathways initiated by LPA and TNF-a that regulate VCAM-1 expression in mesothelial cells; 2) define the contribution of macrophages and mesothelial cells to VCAM-1 expression and ovarian cancer progression; and 3) identify the clinical parameters that correlate with mesothelial VCAM-1 expression in ovarian cancer patients. Understanding the factors that regulate VCAM-1 expression in ovarian cancer patients will provide insights into the design of new opportunities for therapeutic intervention. Successful completion of these aims is expected to provide important mechanistic information about mesothelial cells, which play a critical role in ovarian cancer peritoneal metastasis. Additionally, understanding the mechanisms by which LPA promotes VCAM-1 expression has implications for the treatment of other diseases characterized by chronic VCAM-1 expression, including autoimmunity and atherosclerosis. PUBLIC HEALTH RELEVANCE: The overall goal of our proposal is to understand the mechanisms that regulate VCAM-1 expression in ovarian cancer patients. Information obtained from the successful completion of this proposal will enhance our understanding of the role of LPA and TNF-a signaling pathways in the regulation of VCAM-1 expression, the contribution of macrophages to VCAM-1 expression, and the clinical parameters associated with expression. In addition, our data is expected to provide insight toward the mechanisms that regulate chronic VCAM-1 expression in other conditions including multiple sclerosis, arthritis, asthma, colitis, and atherosclerosis.

描述(申请人提供)：卵巢癌是女性癌症相关死亡的第四大原因。卵巢癌的预后相对较差，反映了确诊时高转移率。事实上，75%的患者被诊断为转移性疾病，其5年存活率为20%-25%。高死亡率在很大程度上是由于转移性癌症缺乏有效的治疗选择。明确调控卵巢癌转移的机制将为卵巢癌的治疗提供急需的额外治疗靶点。我们假设整合素介导的肿瘤细胞和间皮细胞之间的相互作用是卵巢癌进展的重要组成部分。卵巢癌通过侵袭腹膜间皮细胞转移，间皮细胞层排列在腹膜腔内。我们报道了一种调节间皮细胞侵袭的新机制。我们的数据表明，VCAM-1在卵巢癌患者的间皮细胞上优先表达，与其配体A4？1整合素(表达在卵巢癌细胞上)一起在细胞培养系统中促进间皮细胞的侵袭。重要的是，在卵巢癌腹膜转移的小鼠模型中，VCAM-1功能的抑制增加了存活率并降低了肿瘤负担。我们的初步数据表明，溶血磷脂酸(LPA)是一种在卵巢癌患者腹膜中发现的生物活性磷脂，它调节间皮细胞的侵袭和间皮细胞VCAM-1的表达。重要的是，间皮细胞慢性产生LPA会导致结构性的VCAM-1表达，这对其他刺激是不起作用的，包括肿瘤坏死因子-α，一种很好地调节VCAM-1表达的调节因子。这项建议的目的是确定调控卵巢癌患者间皮细胞VCAM-1表达的机制。这项工作的具体目标如下：1)确定LPA和TNF-a启动的调节间皮细胞VCAM-1表达的信号通路；2)确定巨噬细胞和间皮细胞在VCAM-1表达和卵巢癌进展中的作用；3)确定与卵巢癌患者间皮VCAM-1表达相关的临床参数。了解调控卵巢癌患者VCAM-1表达的因素将为设计新的治疗干预机会提供见解。这些目标的成功完成有望提供有关间皮细胞的重要机制信息，间皮细胞在卵巢癌腹膜转移中发挥关键作用。此外，了解LPA促进VCAM-1表达的机制对于其他以慢性VCAM-1表达为特征的疾病的治疗具有重要意义，包括自身免疫和动脉粥样硬化。 公共卫生相关性：我们建议的总体目标是了解卵巢癌患者VCAM-1表达的调节机制。本研究的成功完成将加深我们对LPA和TNF-a信号通路在调节VCAM-1表达中的作用，巨噬细胞对VCAM-1表达的贡献，以及与表达相关的临床参数的理解。此外，我们的数据有望为调节多发性硬化症、关节炎、哮喘、结肠炎和动脉粥样硬化等其他疾病的慢性VCAM-1表达的机制提供洞察力。