组织微阵列
微阵列分析技术
医学
蛋白质前体
生物标志物
癌症研究
癌
纤维蛋白原
病理
微阵列
比例危险模型
生存分析
基底细胞
免疫组织化学
蛋白质组学
肿瘤科
下调和上调
临床意义
细胞
内科学
生物
信使核糖核酸
实时聚合酶链反应
癌症
基因表达
血液蛋白质类
基因表达谱
作者
Mustafa Magan,Xiaolian Gu,Nicola Sgaramella,Karin Nylander
标识
DOI:10.1038/s41598-026-57329-0
摘要
In this study, we aimed to evaluate the prognostic significance of collagens in patients with oral squamous cell carcinoma (OSCC). Plasma proteomics data from 40 OSCC patients and 33 healthy controls, generated using the Olink Explore 3072 platform, along with microarray gene expression data from 29 OSCC tumours, 21 clinically normal tissues contralateral to tumour (NTCT), and 14 healthy controls, were analysed to assess expression levels of collagens and their associations with clinicopathological variables and survival outcomes. Eleven collagen peptides were detected in plasma. Higher circulating levels of collagen type III alpha 1 chain (COL3A1) propeptides were associated with improved overall survival and longer disease-free time (p < 0.05). Penalised Cox regression using the least absolute shrinkage and selection operator (LASSO) supported COL3A1 propeptide as a survival-associated feature. Comparison of protein profiles between COL3A1-low and COL3A1-high patients identified neutrophil degranulation as the most significantly enriched pathway. Microarray differential expression analysis showed COL3A1 mRNA to be significantly upregulated in tumour tissues compared with NTCT and healthy controls (FDR < 0.05). Circulating COL3A1 propeptide shows potential as a prognostic biomarker for OSCC and may reflect systemic immune-related alterations.
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