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The Role of Post Traumatic Stress and Substance P in Melanoma Brain Metastasis

创伤后应激和 P 物质在黑色素瘤脑转移中的作用

基本信息

批准号：
8641676
负责人：
ERIC T WONG
金额：
$ 8.44万
依托单位：
BETH ISRAEL DEACONESS MEDICAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2013
资助国家：
美国
起止时间：
2013-04-01 至 2016-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8641676
关键词：
Animals Anxiety Binding Biological Brain Brain Neoplasms Cancer Patient Cause of Death Cell Line Cell Proliferation Cell Surface Receptors Cells Cerebrospinal Fluid Cessation of life Chemotaxis Cognitive Data Disease Drug Targeting Epigenetic Process Exhibits Genes Growth Hematogenous Hematogenous Spread Human In Vitro Individual Invaded Link Malignant - descriptor Malignant Neoplasms Mediating Mediator of activation protein Melanoma Cell Mental Depression Metastatic malignant neoplasm to brain Molecular Mus Mutation Neoplasm Metastasis Neuraxis Neuropeptides Neurotransmitters Organ Pain Patients Play Primary Neoplasm Process Property Psyche structure Psychological Stress Role Site Skin Source Stimulus Stress Substance P Substance P Receptor TACR1 gene Testing Tissues United States cell motility chemokine enantiomer improved in vivo lymph nodes melanocyte melanoma migration neoplastic cell novel outcome forecast post-traumatic stress preference pressure psychosocial public health relevance receptor restraint stress tumor growth

项目摘要

DESCRIPTION (provided by applicant): Melanoma is one of the most common forms of cancer in the United States. While melanoma originates in the skin, death from this disease is due to its propensity to rapidly metastasize, with a preference to the skin, lymph nodes and brain. In this study we will study the role the cognitive stress may play during the process of melanoma brain metastasis. We have discovered that melanoma brain tumors differ from their lymph node counterparts by the presence of a cell surface receptor for substance P, called NKR1. Substance P is a neurotransmitter involved in pain, anxiety and depression. In melanoma cells isolated from the brain, but not those isolated from other sites in the body, substance P is able to drive migration towards its source and promote their proliferation, suggesting that it plays a specific role in brain metastasis. We have found that stimuli that increase anxiety in mice also promote intracerebral tumor growth and that this process can be inhibited by NK1R antagonists. This raises the possibility that cognitive states such as depression and anxiety may promote melanoma brain metastasis and tumor growth. This study seeks to further test the possible relationship between substance P and NKR1 in this process supported by our current data.

描述（由申请人提供）：黑色素瘤是美国最常见的癌症之一。虽然黑色素瘤起源于皮肤，但这种疾病的死亡是由于其快速转移的倾向，优先转移到皮肤，淋巴结和大脑。在本研究中，我们将研究认知应激在黑色素瘤脑转移过程中可能发挥的作用。我们发现，黑色素瘤脑肿瘤与淋巴结肿瘤的不同之处在于存在一种称为NKR1的P物质细胞表面受体。P物质是一种与疼痛、焦虑和抑郁有关的神经递质。在从大脑分离的黑色素瘤细胞中，而不是从身体其他部位分离的黑色素瘤细胞中，P物质能够驱动向其来源迁移并促进其增殖，这表明它在脑转移中起着特定的作用。我们发现，增加小鼠焦虑的刺激也会促进脑内肿瘤的生长，而这一过程可以被NK1R拮抗剂抑制。这增加了抑郁和焦虑等认知状态可能促进黑色素瘤脑转移和肿瘤生长的可能性。这项研究旨在进一步测试我们目前的数据支持的这一过程中P物质和NKR 1之间的可能关系。