Ellis L M, Takahashi Y, Liu W, Shaheen R M
University of Texas M.D. Anderson Cancer Center, Department of Surgical Oncology, Houston, Texas 77030, USA.
Oncologist. 2000;5 Suppl 1:11-5. doi: 10.1634/theoncologist.5-suppl_1-11.
Tumor growth and metastasis are dependent on angiogenesis. Vascular endothelial growth factor (VEGF) plays an important role in the angiogenesis of numerous solid malignancies including colon cancer. Evidence from preclinical and clinical studies indicates VEGF is the predominant angiogenic factor in human colon cancer and is associated with formation of metastases and poor prognosis. Based on these results, it was hypothesized that inhibition of VEGF receptor activity could inhibit colon cancer liver metastasis. To test this hypothesis, the authors evaluated the ability of a small molecule inhibitor specific for the tyrosine kinase VEGF receptor Flk-1/KDR (SU5416) or multiple tyrosine kinase receptors (SU6668) to inhibit tumor angiogenesis and metastasis in a model of colon cancer hepatic metastasis. Both SU5416 and SU6668 inhibited metastases, microvessel formation, and cell proliferation while increasing tumor cell and endothelial cell apoptosis. These results showed that targeting the VEGF receptor/ligand system is a rational approach to inhibiting tumor growth and prolonging survival.
肿瘤生长和转移依赖于血管生成。血管内皮生长因子(VEGF)在包括结肠癌在内的众多实体恶性肿瘤的血管生成中起重要作用。临床前和临床研究证据表明,VEGF是人类结肠癌中主要的血管生成因子,与转移的形成及不良预后相关。基于这些结果,有人提出抑制VEGF受体活性可能会抑制结肠癌肝转移。为验证这一假设,作者评估了一种对酪氨酸激酶VEGF受体Flk-1/KDR具有特异性的小分子抑制剂(SU5416)或多种酪氨酸激酶受体(SU6668)在结肠癌肝转移模型中抑制肿瘤血管生成和转移的能力。SU5416和SU6668均能抑制转移、微血管形成和细胞增殖,同时增加肿瘤细胞和内皮细胞凋亡。这些结果表明,靶向VEGF受体/配体系统是抑制肿瘤生长和延长生存期的合理方法。