Department of Orthopaedics, University of Melbourne, St. Vincent's Hospital, VIC, Australia.
Expert Opin Ther Pat. 2011 Feb;21(2):121-30. doi: 10.1517/13543776.2011.545347. Epub 2011 Jan 5.
Traditional forms of cancer therapy, which include chemotherapy, have largely been overhauled due to the significant degree of toxicity they pose to normal, otherwise healthy tissue. It is hoped that the use of biological agents, most of which are endogenously present in the body, will lead to safer treatment outcomes, without sacrificing efficacy. The finding that pigment epithelium-derived factor (PEDF), a naturally-occurring protein, is a potent angiogenesis inhibitor has become the basis for studying the role of PEDF in tumours that are highly resistant to chemotherapy. The determination of the direct role of PEDF against cancer paves the way for understanding and developing PEDF as a novel drug. This review focuses on the patent applications behind testing the anticancer therapeutic effect of PEDF via its receptors as an antiangiogenic agent and as a direct anticancer agent. The majority of the PEDF patents describe the antiangiogenic ability and usage of recombinant vectors as the mode of treatment delivery. PEDF's therapeutic potential against different diseases and the discovery of its receptors open possibilities for improving PEDF-based peptide design and drug delivery modes.
传统的癌症治疗形式,包括化疗,由于它们对正常、健康的组织造成的毒性程度很大,已经在很大程度上进行了彻底改革。人们希望使用生物制剂,其中大多数在体内天然存在,将导致更安全的治疗结果,而不牺牲疗效。发现色素上皮衍生因子(PEDF)是一种天然存在的蛋白质,是一种有效的血管生成抑制剂,这成为研究 PEDF 在对化疗高度耐药的肿瘤中的作用的基础。PEDF 对抗癌症的直接作用的确定为理解和开发 PEDF 作为一种新型药物铺平了道路。这篇综述重点介绍了通过其受体作为抗血管生成剂和直接抗癌剂测试 PEDF 的抗癌治疗效果的专利申请。大多数 PEDF 专利描述了重组载体的抗血管生成能力和用途作为治疗输送的模式。PEDF 对不同疾病的治疗潜力及其受体的发现为改进基于 PEDF 的肽设计和药物输送模式开辟了可能性。