Sawyer Tomi K
ARIAD Pharmaceuticals, Cambridge, MA 02139, USA.
Expert Opin Investig Drugs. 2004 Jan;13(1):1-19. doi: 10.1517/13543784.13.1.1.
Cancer metastasis is a significant problem and a tremendous challenge to drug discovery relative to identifying key therapeutic targets as well as developing breakthrough medicines. Recent progress in unravelling the complex molecular circuitry of cancer metastasis, including receptors, intracellular proteins and genes, is highlighted. Furthermore, recent advances in drug discovery to provide novel proof-of-concept ligands, in vivo effective lead compounds and promising clinical candidates, are summarised. Such drug discovery efforts illustrate the integration of functional genomics, cell biology, structural biology, drug design, molecular/cellular screening and chemical diversity (e.g., small molecules, peptides/peptidomimetics, natural products, antisense, vaccines and antibodies). Promising therapeutic targets for cancer metastasis have been identified, including Src, focal adhesion kinase, the integrin receptor, the vascular endothelial growth factor receptor, the epidermal growth factor receptor, Her-2/neu, c-Met, Ras/Rac GTPases, Raf kinase, farnesyl diphosphate synthase (i.e., amino-bisphosphonate therapeutic target) and matrix metalloproteases within the context of their implicated functional roles in cancer growth, invasion, angiogenesis and survival at secondary sites. Clinical and preclinical drug discovery is described and emerging small-molecule inhibitors of protein kinases are highlighted.
相对于确定关键治疗靶点以及开发突破性药物而言,癌症转移是一个重大问题,也是药物研发面临的巨大挑战。本文着重介绍了在揭示癌症转移复杂分子机制方面的最新进展,包括受体、细胞内蛋白质和基因。此外,还总结了药物研发的最新进展,这些进展提供了新的概念验证配体、体内有效的先导化合物和有前景的临床候选药物。此类药物研发工作体现了功能基因组学、细胞生物学、结构生物学、药物设计、分子/细胞筛选和化学多样性(如小分子、肽/肽模拟物、天然产物、反义药物、疫苗和抗体)的整合。已确定了一些有前景的癌症转移治疗靶点,包括Src、粘着斑激酶、整合素受体、血管内皮生长因子受体、表皮生长因子受体、Her-2/neu、c-Met、Ras/Rac GTPases、Raf激酶、法尼基二磷酸合酶(即氨基双膦酸盐治疗靶点)以及基质金属蛋白酶,文中阐述了它们在癌症生长、侵袭、血管生成和在转移部位存活中的相关功能作用。本文还描述了临床和临床前药物研发情况,并着重介绍了新兴的蛋白激酶小分子抑制剂。