Menrad Andreas, Menssen Hans D
Department of AntiAngiogenesis Research, Schering AG, Corporate Business Area Oncology, Germany.
Expert Opin Ther Targets. 2005 Jun;9(3):491-500. doi: 10.1517/14728222.9.3.491.
Chemotherapeutic agents for the treatment of solid cancers do not discriminate between malignant and normal tissue, but rather depend on the increased proliferation of tumour cells versus benign cells. To reach therapeutically active concentrations in the tumour, large doses of these rather unspecific compounds have to be given to the patient, often resulting in severe side effects. Therefore, the goal of modern cancer research is the development of highly selective compounds which are able to discriminate between tumour tissue and normal tissue. One promising approach in this direction is antibody-mediated targeted cancer therapy which may either block an important receptor-ligand interaction or deliver a therapeutically active molecule to an otherwise nonfunctional target. A prerequisite for such an approach is the tumour-selective expression of the respective target structure. This review discusses extra domain-B fibronectin as a promising target which is associated with tumour angiogenesis and tumour growth for the development of novel antibody-mediated therapies.
用于治疗实体癌的化疗药物不会区分恶性组织和正常组织,而是依赖于肿瘤细胞相对于良性细胞的增殖增加。为了在肿瘤中达到治疗活性浓度,必须给患者使用大剂量这些相当非特异性的化合物,这常常导致严重的副作用。因此,现代癌症研究的目标是开发能够区分肿瘤组织和正常组织的高选择性化合物。朝着这个方向的一种有前景的方法是抗体介导的靶向癌症治疗,它可以阻断重要的受体-配体相互作用,或者将治疗活性分子递送至原本无功能的靶点。这种方法的一个先决条件是各自靶结构的肿瘤选择性表达。本综述讨论了额外结构域B纤连蛋白作为一个有前景的靶点,它与肿瘤血管生成和肿瘤生长相关,可用于开发新型抗体介导的疗法。