Arbiser Jack L
Department of Dermatology and Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia, USA.
J Clin Invest. 2007 Oct;117(10):2762-5. doi: 10.1172/JCI33190.
In this issue of the JCI, Nissen et al. report that a reciprocal interaction exists between the growth factors FGF2 and PDGF-BB, causing tumors to exhibit increased angiogenesis and metastatic potential. Both FGF2 and PDGF-BB signal through tyrosine kinase receptors, which have been the target of tyrosine kinase inhibitors for cancer therapies. These inhibitors are usually small molecules that inhibit the kinase activity of a receptor or nonreceptor tyrosine kinase, preventing downstream signaling. The results of this study shed light on why tyrosine kinase inhibitors have been useful for the treatment of only a small number of advanced cancers. Currently, a major focus of pharmaceutical companies is to develop ever more potent and specific tyrosine kinases. The results presented here suggest that this approach may not be successful.
在本期《临床研究杂志》中,尼森等人报告称,生长因子FGF2和PDGF - BB之间存在相互作用,导致肿瘤表现出增强的血管生成和转移潜能。FGF2和PDGF - BB均通过酪氨酸激酶受体发出信号,而酪氨酸激酶受体一直是癌症治疗中酪氨酸激酶抑制剂的作用靶点。这些抑制剂通常是小分子,可抑制受体或非受体酪氨酸激酶的激酶活性,从而阻止下游信号传导。这项研究的结果揭示了为什么酪氨酸激酶抑制剂仅对少数晚期癌症的治疗有效。目前,制药公司的一个主要关注点是开发更有效、更具特异性的酪氨酸激酶。此处呈现的结果表明这种方法可能不会成功。