Trusolino L, Pugliese L, Comoglio P M
Division of Molecular Oncology, IRCC, Institute for Cancer Research, University of Torino School of Medicine, 10060 Candiolo, Torino,
FASEB J. 1998 Oct;12(13):1267-80. doi: 10.1096/fasebj.12.13.1267.
The scatter factors, which include hepatocyte growth factor and macrophage stimulating protein, stand out from other cytokines because of their uncommon biological properties. In addition to promoting cell growth and protection from apoptosis, they are involved in the control of cell dissociation, migration into extracellular matrices, and a unique process of differentiation called 'branching morphogenesis'. Through the concerted regulation of these complex phenomena, scatter factors promote development, regeneration, and reconstruction of normal organ architecture. In transformed epithelia, scatter factors can mediate tumor invasive growth, a harmful feature of neoplastic progression in which cancer cells invade surrounding tissues, penetrate across the vascular walls, and eventually disseminate throughout the body, giving rise to systemic metastases. A much-debated issue in basic biology, which has strong implications for experimental medicine, is how to dissociate the favorable effects of growth factors from their adverse ones. Accordingly, to find agonists or antagonists with potential therapeutic applications is a crucial undertaking for current research. Domain-mapping analyses of growth factor molecules can help to isolate specific structural requirements for the induction of selective biological effects. Based on the observation that certain growth factors must undergo posttranslational modifications to exert a full response, it is possible to interfere with their activation mechanisms to modulate their functions. Finally, the identification of cell type-specific coreceptors able to potentiate their activity allows drawing of a functional body map, where some organs or tissues may be more responsive than others to growth factors. This review is focused on how, and to what extent, scatter factors can behave 'well' or 'badly' according to their molecular structure, the way they are activated, and the way they interact with cell surface receptors and coreceptors.
散射因子,包括肝细胞生长因子和巨噬细胞刺激蛋白,因其独特的生物学特性而有别于其他细胞因子。除了促进细胞生长和保护细胞免于凋亡外,它们还参与细胞解离、迁移到细胞外基质以及一种称为“分支形态发生”的独特分化过程的调控。通过对这些复杂现象的协同调节,散射因子促进正常器官结构的发育、再生和重建。在转化上皮细胞中,散射因子可介导肿瘤侵袭性生长,这是肿瘤进展中的一个有害特征,癌细胞在其中侵袭周围组织、穿透血管壁并最终扩散至全身,导致全身转移。基础生物学中一个备受争议且对实验医学有重要影响的问题是如何区分生长因子的有利作用和不利作用。因此,寻找具有潜在治疗应用的激动剂或拮抗剂是当前研究的一项关键任务。生长因子分子的结构域映射分析有助于分离诱导选择性生物学效应所需的特定结构要求。基于某些生长因子必须经过翻译后修饰才能发挥充分作用这一观察结果,有可能干扰其激活机制以调节其功能。最后,鉴定能够增强其活性的细胞类型特异性共受体有助于绘制功能图谱,其中一些器官或组织可能比其他器官或组织对生长因子更敏感。本综述聚焦于散射因子如何以及在何种程度上根据其分子结构、激活方式以及与细胞表面受体和共受体的相互作用方式表现出“好”或“坏”的作用。