Department of Surgery, Cancer Research Laboratories, St. George Hospital, University of New South Wales, Sydney, NSW 2217, Australia.
Med Res Rev. 2014 Sep;34(5):918-56. doi: 10.1002/med.21308. Epub 2014 Feb 18.
Currently, there are several studies supporting the role of urokinase-type plasminogen activator (uPA) system in cancer. The association of uPA to its receptor triggers the conversion of plasminogen into plasmin. This process is regulated by the uPA inhibitors (PAI-1 and PAI-2). Plasmin promotes degradation of basement membrane and extracellular matrix (ECM) components as well as activation of ECM latent matrix metalloproteases. Degradation and remodeling of the surrounding tissues is crucial in the early steps of tumor progression by facilitating expansion of the tumor mass, release of tumor growth factors, activation of cytokines as well as induction of tumor cell proliferation, migration, and invasion. Hence, many tumors showed a correlation between uPA system component levels and tumor aggressiveness and survival. Therefore, this review summarizes the structure of the uPA system, its contribution to cancer progression, and the clinical relevance of uPA family members in cancer diagnosis. In addition, the review evaluates the significance of uPA system in the development of cancer-targeted therapies.
目前,有几项研究支持尿激酶型纤溶酶原激活物(uPA)系统在癌症中的作用。uPA 与其受体的结合触发纤溶酶原转化为纤溶酶。这一过程受 uPA 抑制剂(PAI-1 和 PAI-2)的调节。纤溶酶促进基底膜和细胞外基质(ECM)成分的降解以及 ECM 潜伏基质金属蛋白酶的激活。周围组织的降解和重塑在肿瘤进展的早期步骤中至关重要,它促进肿瘤体积的扩大、肿瘤生长因子的释放、细胞因子的激活以及诱导肿瘤细胞的增殖、迁移和浸润。因此,许多肿瘤显示 uPA 系统成分水平与肿瘤侵袭性和存活率之间存在相关性。因此,本综述总结了 uPA 系统的结构、它在癌症进展中的作用以及 uPA 家族成员在癌症诊断中的临床相关性。此外,该综述评估了 uPA 系统在癌症靶向治疗发展中的意义。