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Roles of inflammation-driven chemokines in the pathogenesis of ovarian cancer

炎症驱动的趋化因子在卵巢癌发病机制中的作用

基本信息

批准号：
7939737
负责人：
DEOK-SOO SON
金额：
$ 36.26万
依托单位：
MEHARRY MEDICAL COLLEGE
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-09-30 至 2014-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7939737
关键词：
1-Phosphatidylinositol 3-Kinase Anti-Inflammatory Agents Anti-inflammatory Ascites Aspirin Attenuated Automobile Driving Basic Science Binding Bioinformatics Biological Markers Biomedical Research CXCL1 gene Cancer Etiology Cell Proliferation Cessation of life Chronic Clinical Collaborations Core Facility Data Development Diagnosis Disease Endocrine Environment Epidermal Growth Factor Receptor Epithelial Epithelial Cells Equipment Etiology Event Exposure to Flow Cytometry Foundations Funding Funding Mechanisms Future Genes Genetic Goals Growth Growth and Development function Gynecologic Oncology IL8RB gene In Vitro Infiltration Inflammation Inflammatory Interleukin-8B Receptor Intraperitoneal Injections Knockout Mice Laboratories Lead Letters Leukocytes Link Mainstreaming Malignant - descriptor Malignant Neoplasms Malignant neoplasm of ovary Manuscripts Measures Methods Minority Mitogen-Activated Protein Kinases Modification Molecular Molecular Biology Molecular Target Morbidity - disease rate Mus Mutation Nuclear Oncogenes Ovarian Ovary Paper Pathogenesis Pathway interactions Patient Care Patients Peer Review Peritoneal Pharmaceutical Preparations Plasma Postdoctoral Fellow Prevention Probability Process Proto-Oncogene Proteins c-akt Publications Publishing Receptor Activation Receptor Signaling Research Research Personnel Resources Role Scientist Serine Signal Transduction Son Staging Stimulus Students System TP53 gene Techniques Therapeutic Threonine Time Training Transfection Tumor Burden Tumor Cell Invasion Tumor Necrosis Factor-alpha Tumor Necrosis Factors Tumor Suppressor Genes Universities Vascular Endothelial Growth Factors Veterinarians Western Blotting Woman Women&apos s Health Work Yang angiogenesis animal care cancer cell cancer risk carcinogenesis cell growth chemokine chemokine receptor cytokine female reproductive system improved in vitro Assay in vivo inhibitor/antagonist medical schools member migration mortality novel novel therapeutics overexpression planetary Atmosphere prevent programs public health relevance research study response restoration square foot tissue culture tumor tumor growth tumor progression tumorigenic

项目摘要

DESCRIPTION (provided by applicant): Ovarian cancer is the fifth leading cause of cancer deaths among women because this deadly insidious disease is typically asymptomatic until the malignancy has reached beyond the ovaries. Although the precise etiology remains unknown, the increasing evidence indicates ovarian cancer is one of inflammation-associated cancers derived from inflammatory diseases. Compared with normal ovarian epithelial cells, ovarian cancer cells expressed highly tumor necrosis factor-1 (TNF) as a main proinflammatory cytokine that controls directly or indirectly chemokine networks. Growth-regulated oncogene (CXCL1) was significantly increased in ovarian cancer cells, and in the plasma and ascites of patients with ovarian cancer. Our recent studies have resulted that CXCL1, 2 and 8 are main inflammation-driven chemokines produced primarily and abundantly from ovarian cancer cells in response to inflammation. In other system, CXCL1 binds its specific receptor (CXCR2) and exert several functional roles such as cell proliferation, invasion, tumor formation and angiogenesis, which may be critical in the pathogenesis of ovarian cancer. These facts support that inflammation-driven chemokines promote ovarian cancer through inflammatory tumor microenvironments, which lead to massive ascites and widespread peritoneal dissemination as described in advanced ovarian cancer followed by the high mortality rate. In particular, genetic modifications such as p53 inactivity and EGFR/Akt overexpression are frequent in high- grade malignant ovarian cancer. The genetic modifications potentiate inflammation- driven chemokines, probably exacerbating the pathogenesis of ovarian cancer. However, the mechanisms inflammation-driven chemokines contribute to the pathogenesis of ovarian cancer are still poorly understood. The long-range goal of this research is to determine the specific contribution of chemokine networks to ovarian carcinogenesis. Targeting inflammation-driven chemokines will lead to a better understanding of the pathogenesis of ovarian cancer and provide important future applications for the potential use of chemokines as a biomarker and for use of specific chemokine receptor inhibitors and anti-inflammatory agents in the prevention and treatment of ovarian cancer. Preventing peritoneal dissemination and ameliorating ascites through blockage of inflammation-driven chemokines improve patient care and overall survival of women with ovarian cancer and other tumors related to inflammation. PUBLIC HEALTH RELEVANCE: Ovarian cancer is often diagnosed at an advanced stage after the cancer has spread beyond the ovary and results to the highest mortality of all cancers of the female reproductive system. Although the precise etiology remains unknown, the increasing evidence has emerged to indicate an impact of inflammation in the development, growth and progression of ovarian cancer. This project to define roles of inflammation-driven chemokines in the pathogenesis of ovarian cancer will provide a firm foundation for future long-term survival reducing ovarian cancer risks and help to envisage much- needed novel therapies for ovarian cancer and other tumors related to inflammation.

描述（由申请人提供）：卵巢癌是女性癌症死亡的第五大原因，因为这种致命的隐匿性疾病通常无症状，直到恶性肿瘤已经超出卵巢。虽然确切的病因尚不清楚，但越来越多的证据表明卵巢癌是由炎症性疾病发展而来的炎症相关性肿瘤之一。与正常卵巢上皮细胞相比，卵巢癌细胞高表达肿瘤坏死因子-1（TNF），TNF是一种主要的促炎细胞因子，直接或间接控制趋化因子网络。生长调节癌基因（CXCL 1）在卵巢癌细胞中，卵巢癌患者的血浆和腹水中显著增加。我们最近的研究表明，CXCL 1，2和8是主要的炎症驱动的趋化因子，主要由卵巢癌细胞在炎症反应中大量产生。在其他系统中，CXCL 1与其特异性受体CXCR 2结合，发挥多种功能作用，如细胞增殖、侵袭、肿瘤形成和血管生成，这可能在卵巢癌的发病机制中起关键作用。这些事实支持炎症驱动的趋化因子通过炎症性肿瘤微环境促进卵巢癌，这导致大量腹水和广泛的腹膜播散，如晚期卵巢癌中所述，随后是高死亡率。特别是，基因修饰如p53失活和EGFR/Akt过表达在高度恶性卵巢癌中很常见.基因修饰增强了炎症驱动的趋化因子，可能加剧了卵巢癌的发病机制。然而，炎症驱动的趋化因子导致卵巢癌发病的机制仍然知之甚少。这项研究的长期目标是确定趋化因子网络对卵巢癌发生的具体贡献。靶向炎症驱动的趋化因子将导致更好地了解卵巢癌的发病机制，并为趋化因子作为生物标志物的潜在用途以及在预防和治疗卵巢癌中使用特异性趋化因子受体抑制剂和抗炎剂提供重要的未来应用。通过阻断炎症驱动的趋化因子来预防腹膜播散和改善腹水，改善卵巢癌和其他炎症相关肿瘤患者的护理和总体生存率。公共卫生关系：卵巢癌通常在癌症已经扩散到卵巢以外的晚期阶段被诊断出来，并且导致女性生殖系统所有癌症中死亡率最高。虽然确切的病因尚不清楚，但越来越多的证据表明炎症在卵巢癌的发展，生长和进展中的影响。该项目旨在确定炎症驱动的趋化因子在卵巢癌发病机制中的作用，将为未来长期生存提供坚实的基础，降低卵巢癌风险，并有助于设想卵巢癌和其他炎症相关肿瘤急需的新疗法。