Hoekman K
Department of Medical Oncology, Academisch Ziekenhuis, Vrije Universiteit, Amsterdam, The Netherlands.
Cancer J. 2001 Nov-Dec;7 Suppl 3:S134-8.
Angiogenesis plays a critical role in the growth and metastasis of solid and hematologic malignancies. This complex and highly regulated process involves numerous different cell types and mediators. Vascular endothelial growth factor, basic fibroblast growth factor, and platelet-derived growth factor are among the soluble factors that stimulate this process. They are ligands for specific tyrosine kinase receptors that are important in transduction of intracellular signals and induction of angiogenesis. SU6668 is a novel molecule that competitively inhibits the tyrosine kinase of the receptors for vascular endothelial growth factor, basic fibroblast growth factor, platelet-derived growth factor, and c-kit. In vitro studies have confirmed that SU6668 inhibits growth factor-stimulated tyrosine phosphorylation. SU6668 also has significant antitumor activity against many types of tumor xenograft explants in athymic mice. SU6668 inhibits angiogenesis through several mechanisms, including the induction of apoptosis in vascular endothelial cells and tumor cells. Currently, Phase 1 studies are being initiated to evaluate the potential of SU6668 as an anticancer agent for humans.
血管生成在实体瘤和血液系统恶性肿瘤的生长及转移过程中发挥着关键作用。这一复杂且高度受调控的过程涉及众多不同的细胞类型和介质。血管内皮生长因子、碱性成纤维细胞生长因子以及血小板衍生生长因子均属于刺激该过程的可溶性因子。它们是特定酪氨酸激酶受体的配体,这些受体在细胞内信号转导及血管生成诱导过程中至关重要。SU6668是一种新型分子,它能竞争性抑制血管内皮生长因子、碱性成纤维细胞生长因子、血小板衍生生长因子以及c-kit受体的酪氨酸激酶。体外研究证实,SU6668可抑制生长因子刺激的酪氨酸磷酸化。SU6668对无胸腺小鼠体内多种类型的肿瘤异种移植外植体也具有显著的抗肿瘤活性。SU6668通过多种机制抑制血管生成,包括诱导血管内皮细胞和肿瘤细胞凋亡。目前,正在开展1期研究以评估SU6668作为人类抗癌药物的潜力。