结直肠癌
外体
医学
微泡
生物标志物
内科学
肿瘤科
比例危险模型
小RNA
癌变
癌症
转移
混淆
生存分析
阶段(地层学)
生物
基因
古生物学
生物化学
作者
Shushan Yan,Ye Jiang,Caihong Liang,Min Cheng,Chengwen Jin,Quanhong Duan,Donghua Xu,Lu Yang,Xiaoyu Zhang,Bin Ren,Peng Jin
摘要
Abstract Accumulating data have suggested exosome‐delivered microRNAs (miRNAs) play critical role in carcinogenesis and cancer progression. However, little is known about the influence of exosomal miR‐6803‐5p on the development and prognosis of colorectal cancer (CRC). Levels of serum exosomal miR‐6803‐5p were determined by microarray analysis and verified by quantitative real‐time PCR (qRT‐PCR). Outcomes of overall survival (OS) and disease‐free survival (DFS) of CRC patients were estimated by Kaplan‐Meier analysis. We used cox regression analysis to investigate the association between exosomes‐encapsulated miR‐6803‐5p and the clinicopathological factors of CRC patients. The exosomal miR‐6803‐5p was significantly increased in serum samples from patients with CRC in contrast to healthy controls. Significantly higher levels of serum exosomal miR‐6803‐5p were observed in CRC patients at later TNM stage or with lymph node metastasis as well as liver metastasis. Patients with elevated levels of serum exosomal miR‐6803‐5p had much poorer OS and DFS. Cox regression analysis revealed high levels of exosomal miR‐6803‐5p was associated with poor prognosis in CRC independent of other confounding factors. Thus, exosomal miR‐6803‐5p is a potential diagnostic and prognostic biomarker for patients with CRC.
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