Department of Genetics, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, 0310 Oslo, Norway.
Mol Oncol. 2010 Apr;4(2):98-118. doi: 10.1016/j.molonc.2009.12.001. Epub 2009 Dec 11.
Glycosylation is the stepwise procedure of covalent attachment of oligosaccharide chains to proteins or lipids, and alterations in this process have been associated with malignant transformation. Simultaneous analysis of the expression of all glycan-related genes clearly gives the advantage of enabling a comprehensive view of the genetic background of the glycobiological changes in cancer cells. Studies focusing on the expression of the whole glycome have now become possible, which prompted us to review the present knowledge on glycosylation in relation to breast cancer diagnosis and progression, in the light of available expression data from tumors and breast tissue of healthy individuals. We used various data resources to select a set of 419 functionally relevant genes involved in synthesis, degradation and binding of N-linked and O-linked glycans, Lewis antigens, glycosaminoglycans (chondroitin, heparin and keratan sulfate in addition to hyaluronan) and glycosphingolipids. Such glycans are involved in a number of processes relevant to carcinogenesis, including regulation of growth factors/growth factor receptors, cell-cell adhesion and motility as well as immune system modulation. Expression analysis of these glycan-related genes revealed that mRNA levels for many of them differ significantly between normal and malignant breast tissue. An associative analysis of these genes in the context of current knowledge of their function in protein glycosylation and connection(s) to cancer indicated that synthesis, degradation and adhesion mediated by glycans may be altered drastically in mammary carcinomas. Although further analysis is needed to assess how changes in mRNA levels of glycan genes influence a cell's glycome and the precise role that such altered glycan structures play in the pathogenesis of the disease, lessons drawn from this study may help in determining directions for future research in the rapidly-developing field of glycobiology.
糖基化是将寡糖链共价连接到蛋白质或脂质的逐步过程,并且该过程的改变与恶性转化有关。同时分析所有与聚糖相关的基因的表达显然具有使人们能够全面了解癌细胞中糖生物学变化的遗传背景的优势。现在已经可以进行专注于整个糖组表达的研究,这促使我们根据来自肿瘤和健康个体的乳腺组织的现有表达数据,综述糖基化与乳腺癌诊断和进展的关系的现有知识。我们使用了各种数据资源来选择一组 419 个与 N-连接和 O-连接聚糖、Lewis 抗原、糖胺聚糖(除透明质酸外还包括软骨素、肝素和硫酸角质素)和糖脂的合成、降解和结合相关的功能相关基因。这些聚糖参与了与致癌作用相关的许多过程,包括调节生长因子/生长因子受体、细胞-细胞粘附和运动以及免疫系统调节。这些与聚糖相关的基因的表达分析表明,它们的 mRNA 水平在正常和恶性乳腺组织之间存在显著差异。在当前对其在蛋白质糖基化中的功能的了解以及与癌症的连接的背景下,对这些基因进行关联分析表明,糖介导的合成、降解和粘附可能在乳腺癌中发生剧烈改变。尽管需要进一步分析来评估聚糖基因的 mRNA 水平变化如何影响细胞的糖组以及这些改变的聚糖结构在疾病发病机制中的精确作用,但从这项研究中吸取的教训可能有助于确定在快速发展的糖生物学领域中未来研究的方向。