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质谱分析揭示了N-聚糖模式与上皮性卵巢癌进展的关联。

Mass spectrometric profiling reveals association of N-glycan patterns with epithelial ovarian cancer progression.

作者信息

Chen Huanhuan, Deng Zaian, Huang Chuncui, Wu Hongmei, Zhao Xia, Li Yan

机构信息

1 Key Laboratory of Marine Drugs, Ministry of Education, Shandong Provincial Key Laboratory of Glycoscience and Glycoengineering, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.

2 Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

Tumour Biol. 2017 Jul;39(7):1010428317716249. doi: 10.1177/1010428317716249.

Abstract

Aberrant changes of N-glycan modifications on proteins have been linked to various diseases including different cancers, suggesting possible avenue for exploring their etiologies based on N-glycomic analysis. Changes in N-glycan patterns during epithelial ovarian cancer development have so far been investigated mainly using serum, plasma, ascites, and cell lines. However, changes in patterns of N-glycans in tumor tissues during epithelial ovarian cancer progression have remained largely undefined. To investigate whether changes in N-glycan patterns correlate with oncogenesis and progression of epithelial ovarian cancer, we profiled N-glycans from formalin-fixed paraffin-embedded tissue slides using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and quantitatively compared among different pathological grades of epithelial ovarian cancer and healthy controls. Our results show that among the 80 compositions of N-glycan detected, expression levels of high-mannose type were higher in epithelial ovarian cancer samples than that observed in healthy controls, accompanied by reduced levels of hybrid-type glycans. By applying receiver operating characteristic analysis, we show that a combined panel composed of four high-mannose and three fucosylated neutral complex N-glycans allows for good discrimination of epithelial ovarian cancer from healthy controls. Furthermore, using a statistical analysis of variance assay, we found that different N-glycan patterns, including 2 high-mannose-type, 2 fucosylated and sialylated complex structures, and 10 fucosylated neutral complex N-glycans, exhibited specific changes in N-glycan abundance across epithelial ovarian cancer grades. Together, our results provide strong evidence that N-glycomic changes are a strong indicator for epithelial ovarian cancer pathological grades and should provide avenues to identify novel biomarkers for epithelial ovarian cancer diagnosis and monitoring.

摘要

蛋白质上N-聚糖修饰的异常变化与包括不同癌症在内的多种疾病有关,这表明基于N-糖组分析探索其病因可能有途径。迄今为止,上皮性卵巢癌发展过程中N-聚糖模式的变化主要通过血清、血浆、腹水和细胞系进行研究。然而,上皮性卵巢癌进展过程中肿瘤组织中N-聚糖模式的变化在很大程度上仍不明确。为了研究N-聚糖模式的变化是否与上皮性卵巢癌的发生和进展相关,我们使用基质辅助激光解吸/电离飞行时间质谱对福尔马林固定石蜡包埋组织切片中的N-聚糖进行了分析,并对不同病理分级的上皮性卵巢癌和健康对照进行了定量比较。我们的结果表明,在检测到的80种N-聚糖组成中,上皮性卵巢癌样本中高甘露糖型的表达水平高于健康对照,同时杂合型聚糖水平降低。通过应用受试者工作特征分析,我们表明,由四种高甘露糖型和三种岩藻糖基化中性复合N-聚糖组成的联合检测 panel 能够很好地区分上皮性卵巢癌和健康对照。此外,通过方差分析,我们发现不同的N-聚糖模式,包括2种高甘露糖型、2种岩藻糖基化和唾液酸化复合结构以及10种岩藻糖基化中性复合N-聚糖,在上皮性卵巢癌分级中N-聚糖丰度呈现特定变化。总之,我们的结果提供了强有力的证据,表明N-糖组变化是上皮性卵巢癌病理分级的有力指标,应为鉴定上皮性卵巢癌诊断和监测的新型生物标志物提供途径。

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