Okolicsanyi Rachel K, Buffiere Anne, Jacinto Jose M E, Chacon-Cortes Diego, Chambers Suzanne K, Youl Philippa H, Haupt Larisa M, Griffiths Lyn R
Genomics Research Centre, Institute for Health and Biomedical Innovation, Queensland University of Technology, Musk Avenue, Kelvin Grove, Brisbane, QLD, 4059, Australia.
Tumour Biol. 2015 Mar;36(3):1731-8. doi: 10.1007/s13277-014-2774-3. Epub 2014 Nov 1.
Breast cancer is a common disease in both developing and developed countries with early identification and treatment improving prognosis and survival. Heparan sulfate proteoglycans (HSPGs) are key components of the extracellular matrix (ECM) that mediate cell adhesion, motility, proliferation, invasion and cell signalling. Members of the syndecan family of HSPGs have been identified to be involved in breast cancer progression through their varied interactions with a number of growth factors, ligands and receptors. Specifically, high expression levels of syndecan-1 (SDC1) have been demonstrated in more invasive breast tumours while elevated syndecan-4 (SDC4) levels have been identified to correspond with improved prognosis. With genetic changes in the syndecans and their association with breast cancers plausible, we examined two single nucleotide polymorphisms in SDC1 (rs1131351) and SDC4 (rs67068737) within an Australian Caucasian breast cancer case/control population. No association was found with SDC4 and breast cancer in our population. However, a significant association between SDC1 and breast cancer was identified in both our case/control population and in a replication cohort. When both populations were combined for analysis, this association became more significant (genotype, p = 0.0003; allele, p = 0.0001). This data suggests an increased risk of developing breast cancer associated with the presence of the C allele of the SDC1 rs1131351 single nucleotide polymorphism (SNP) and may provide a marker toward early breast cancer detection.
乳腺癌在发展中国家和发达国家都是一种常见疾病,早期识别和治疗可改善预后和生存率。硫酸乙酰肝素蛋白聚糖(HSPGs)是细胞外基质(ECM)的关键组成部分,介导细胞黏附、运动、增殖、侵袭和细胞信号传导。已确定HSPGs的syndecan家族成员通过与多种生长因子、配体和受体的不同相互作用参与乳腺癌进展。具体而言,在侵袭性更强的乳腺肿瘤中已证实syndecan-1(SDC1)表达水平较高,而syndecan-4(SDC4)水平升高与预后改善相关。鉴于syndecans的基因变化及其与乳腺癌的关联具有合理性,我们在澳大利亚白种人乳腺癌病例/对照人群中检测了SDC1(rs1131351)和SDC4(rs67068737)中的两个单核苷酸多态性。在我们的人群中未发现SDC4与乳腺癌有关联。然而,在我们的病例/对照人群以及一个重复队列中均发现SDC1与乳腺癌存在显著关联。当将两个群体合并进行分析时,这种关联变得更加显著(基因型,p = 0.0003;等位基因,p = 0.0001)。该数据表明,与SDC1 rs1131351单核苷酸多态性(SNP)的C等位基因存在相关的患乳腺癌风险增加,并且可能为早期乳腺癌检测提供一个标志物。