Kuba K, Matsumoto K, Date K, Shimura H, Tanaka M, Nakamura T
Department of Oncology, Biomedical Research Center, Osaka University Medical School, Suita, Japan.
Cancer Res. 2000 Dec 1;60(23):6737-43.
We reported that NK4, composed of the N-terminal hairpin and subsequent four kringle domains of hepatocyte growth factor (HGF), acts as the competitive antagonist for HGF. We now provide the first evidence that NK4 inhibits tumor growth and metastasis as an angiogenesis inhibitor as well as an HGF antagonist. Administration of NK4 suppressed primary tumor growth and lung metastasis of Lewis lung carcinoma and Jyg-MC(A) mammary carcinoma s.c. implanted into mice, although neither HGF nor NK4 affected proliferation and survival of these tumor cells in vitro. NK4 treatment resulted in a remarkable decrease in microvessel density and an increase of apoptotic tumor cells in primary tumors, which suggests that the inhibition of primary tumor growth by NK4 may be achieved by suppression of tumor angiogenesis. In vivo, NK4 inhibited angiogenesis in chick chorioallantoic membranes and in rabbit corneal neovascularization induced by basic fibroblast growth factor (bFGF). In vitro, NK4 inhibited growth and migration of human microvascular endothelial cells induced by bFGF and vascular endothelial growth factor (VEGF) as well as by HGF. HGF and VEGF activated the Met/HGF receptor and the KDR/VEGF receptor, respectively, whereas NK4 inhibited HGF-induced Met tyrosine phosphorylation but not VEGF-induced KDR phosphorylation. NK4 inhibited HGF-induced ERK1/2 (p44/42 mitogen-activated protein kinase) activation, but allowed for bFGF- and VEGF-induced ERK1/2 activation. These results indicate that NK4 is an angiogenesis inhibitor as well as an HGF antagonist, and that the antiangiogenic action of NK4 is independent of its activity as HGF antagonist. The bifunctional properties of NK4 to act as an angiogenesis inhibitor and as an HGF antagonist raises the possibility that NK4 may prove therapeutic for cancer patients.
我们曾报道,由肝细胞生长因子(HGF)的N端发夹结构和随后的四个kringle结构域组成的NK4,可作为HGF的竞争性拮抗剂。我们现在提供首个证据表明,NK4作为一种血管生成抑制剂以及HGF拮抗剂,可抑制肿瘤生长和转移。给予NK4可抑制皮下植入小鼠的Lewis肺癌和Jyg-MC(A)乳腺癌的原发肿瘤生长及肺转移,尽管HGF和NK4在体外均不影响这些肿瘤细胞的增殖和存活。NK4处理导致原发肿瘤中微血管密度显著降低,凋亡肿瘤细胞增加,这表明NK4对原发肿瘤生长的抑制可能是通过抑制肿瘤血管生成实现的。在体内,NK4可抑制鸡胚绒毛尿囊膜和碱性成纤维细胞生长因子(bFGF)诱导的兔角膜新生血管中的血管生成。在体外,NK4可抑制bFGF、血管内皮生长因子(VEGF)以及HGF诱导的人微血管内皮细胞的生长和迁移。HGF和VEGF分别激活Met/HGF受体和KDR/VEGF受体,而NK4可抑制HGF诱导的Met酪氨酸磷酸化,但不抑制VEGF诱导的KDR磷酸化。NK4可抑制HGF诱导的ERK1/2(p44/42丝裂原活化蛋白激酶)激活,但不影响bFGF和VEGF诱导的ERK1/2激活。这些结果表明,NK4是一种血管生成抑制剂以及HGF拮抗剂,且NK4的抗血管生成作用与其作为HGF拮抗剂的活性无关。NK4作为血管生成抑制剂和HGF拮抗剂的双重功能特性增加了其可能对癌症患者具有治疗作用的可能性。