Tomao Federica, Papa Anselmo, Rossi Luigi, Caruso Davide, Zoratto Federica, Benedetti Panici Pierluigi, Tomao Silverio
'Sapienza' University of Rome, Department of Gynaecology and Obstetrics, Policlinico 'Umberto I' , Rome , Italy
Expert Opin Investig Drugs. 2014 Jan;23(1):37-53. doi: 10.1517/13543784.2013.839657. Epub 2013 Oct 11.
Ovarian cancer is the most lethal gynecological cancer, mainly because of the advanced stage of the disease at diagnosis, with recent research investigating novel targets and agents into the clinical practice, with the aim to improve prognosis and quality of life. Angiogenesis is a significant target for ovarian cancer therapy.
Areas covered in this review include the most common molecular pathways of angiogenesis, which have provided novel targets for tailored therapy in ovarian cancer patients. These therapeutic strategies comprise monoclonal antibodies and tyrosine kinase inhibitors. These drugs have as molecular targets such as vascular endothelial growth factor (VEGF), VEGF receptor, platelet-derived growth factor, fibroblast growth factor, angiopoietin and Ephrin type-A receptor 2.
The expansion in understanding the molecular biology that characterizes cancer cells has led to the rapid development of new agents to target important pathways, but the heterogeneity of ovarian cancer biology indicates that there is no predominant defect. This review attempts to discuss progress till date in tackling a more general target applicable to ovarian cancer angiogenesis.
卵巢癌是最致命的妇科癌症,主要原因是在诊断时疾病已处于晚期。最近的研究正在探索新的靶点和药物并将其应用于临床实践,旨在改善预后和生活质量。血管生成是卵巢癌治疗的一个重要靶点。
本综述涵盖的领域包括血管生成最常见的分子途径,这些途径为卵巢癌患者的个体化治疗提供了新的靶点。这些治疗策略包括单克隆抗体和酪氨酸激酶抑制剂。这些药物的分子靶点包括血管内皮生长因子(VEGF)、VEGF受体、血小板衍生生长因子、成纤维细胞生长因子、血管生成素和Ephrin A2型受体。
对癌细胞特征性分子生物学认识的扩展导致了针对重要途径的新药物的快速发展,但卵巢癌生物学的异质性表明不存在主要缺陷。本综述试图讨论迄今为止在攻克适用于卵巢癌血管生成的更通用靶点方面取得的进展。