Nikitovic Dragana, Berdiaki Aikaterini, Spyridaki Ioanna, Krasanakis Theodoros, Tsatsakis Aristidis, Tzanakakis George N
Laboratory of Anatomy-Histology-Embryology, Medical School, University of Crete, Heraklion, Greece.
Laboratory of Toxicology, Medical School, University of Crete, Heraklion, Greece.
Front Endocrinol (Lausanne). 2018 Mar 6;9:69. doi: 10.3389/fendo.2018.00069. eCollection 2018.
Proteoglycans (PGs), important constituents of the extracellular matrix, have been associated with cancer pathogenesis. Their unique structure consisting of a protein core and glycosaminoglycan chains endowed with fine modifications constitutes these molecules as capable cellular effectors important for homeostasis and contributing to disease progression. Indeed, differential expression of PGs and their interacting proteins has been characterized as specific for disease evolvement in various cancer types. Importantly, PGs to a large extent regulate the bioavailability of hormones, growth factors, and cytokines as well as the activation of their respective receptors which regulate phenotypic diversibility, gene expression and rates of recurrence in specific tumor types. Defining and targeting these effectors on an individual patient basis offers ground for the development of newer therapeutic approaches which may act as either supportive or a substitute treatment to the standard therapy protocols. This review discusses the roles of PGs in cancer progression, developing technologies utilized for the defining of the PG "signature" in disease, and how this may facilitate the generation of tailor-made cancer strategies.
蛋白聚糖(PGs)是细胞外基质的重要组成部分,与癌症发病机制有关。它们独特的结构由一个蛋白质核心和带有精细修饰的糖胺聚糖链组成,使这些分子成为对体内平衡重要且有助于疾病进展的有能力的细胞效应器。事实上,PGs及其相互作用蛋白的差异表达已被表征为各种癌症类型中疾病演变的特异性特征。重要的是,PGs在很大程度上调节激素、生长因子和细胞因子的生物利用度以及它们各自受体的激活,这些受体调节特定肿瘤类型中的表型多样性、基因表达和复发率。在个体患者基础上定义和靶向这些效应器为开发更新的治疗方法提供了依据,这些方法可以作为标准治疗方案的支持性或替代治疗。本综述讨论了PGs在癌症进展中的作用、用于定义疾病中PG“特征”的开发技术,以及这如何促进量身定制的癌症策略的产生。