Cardiff University, UK.
Anticancer Agents Med Chem. 2010 Jan;10(1):47-57. doi: 10.2174/1871520611009010047.
Hepatocyte growth factor (HGF) plays a plethora of roles in the progression of many invasive and metastatic cancers. The interaction between tumour cells and their surrounding stromal environment remains a crucial factor governing tumour invasion and metastasis. HGF is primarily synthesised by stromal fibroblasts as an inactive precursor known as pro-HGF. A number of proteases have demonstrated the ability to convert pro-HGF into the biologically active form of HGF, although the two main factors responsible are HGF activator (HGFA) and matriptase. The HGF activation inhibitors (HAI-1 and HAI-2) are two novel Kunitz-type serine protease inhibitors that regulate HGFA and matriptase activity to govern the influence of HGF within the body. Deregulation of HAI expression can lead to shift in the HGF activation/inhibition balance ratio in favour of enhanced HGF production. Therefore, these HGF activation inhibitors may have a direct bearing on cancer invasion and metastasis. This review examines the accumulating evidence on the emerging role and therapeutic potential of HAI-1 and HAI-2 in cancer.
肝细胞生长因子 (HGF) 在许多侵袭性和转移性癌症的进展中发挥着多种作用。肿瘤细胞与其周围基质环境之间的相互作用仍然是控制肿瘤侵袭和转移的关键因素。HGF 主要由基质成纤维细胞合成,作为一种称为前 HGF 的无活性前体。许多蛋白酶已证明能够将前 HGF 转化为具有生物活性的 HGF 形式,尽管负责的两个主要因素是 HGF 激活剂 (HGFA) 和基质金属蛋白酶。HGF 激活抑制剂 (HAI-1 和 HAI-2) 是两种新型的 Kunitz 型丝氨酸蛋白酶抑制剂,可调节 HGFA 和基质金属蛋白酶的活性,以控制体内 HGF 的影响。HAI 表达的失调可能导致 HGF 激活/抑制平衡比值向增强 HGF 产生的方向转变。因此,这些 HGF 激活抑制剂可能对癌症的侵袭和转移有直接影响。本文综述了 HAI-1 和 HAI-2 在癌症中的作用和治疗潜力的研究进展。