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细胞外囊泡相关重复元件 DNA 作为骨肉瘤的候选生物标志物。

Extracellular vesicle-associated repetitive element DNAs as candidate osteosarcoma biomarkers.

机构信息

The Vision Center and The Saban Research Institute, Children's Hospital Los Angeles, 4650 Sunset Blvd, MS163, Los Angeles, CA, 90027, USA.

Cancer Biology and Genomics Program, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90089, USA.

出版信息

Sci Rep. 2021 Jan 8;11(1):94. doi: 10.1038/s41598-020-77398-z.

Abstract

Osteosarcoma (OS) is the most common malignant bone tumor in children and young adults. Despite that high-risk factors have been identified, no test for early detection is available. This study aimed to identify circulating nucleic acid sequences associated with serum extracellular vesicle (EV) preparations at the time of OS diagnosis, as a step towards an OS early detection assay. Sequencing of small nucleic acids extracted from serum EV preparations revealed increased representation of diverse repetitive element sequences in OS patient versus control sera. Analysis of a validation cohort using qPCR of PEG-precipitated EV preparations revealed the over-representation of HSATI, HSATII, LINE1-P1, and Charlie 3 at the DNA but not RNA level, with receiver operating characteristic (ROC) area under the curve (AUC) ≥ 0.90. HSATI and HSATII DNAs co-purified with EVs prepared by precipitation and size exclusion chromatography but not by exosome immunocapture, indicative of packaging in a non-exosomal complex. The consistent over-representation of EV-associated repetitive element DNA sequences suggests their potential utility as biomarkers for OS and perhaps other cancers.

摘要

骨肉瘤(OS)是儿童和青少年中最常见的恶性骨肿瘤。尽管已经确定了高危因素,但目前尚无早期检测的方法。本研究旨在鉴定与 OS 诊断时血清细胞外囊泡(EV)制剂相关的循环核酸序列,作为开发 OS 早期检测方法的一个步骤。从血清 EV 制剂中提取的小核酸测序显示,OS 患者血清中多种重复元件序列的代表性增加。使用 PEG 沉淀 EV 制剂的 qPCR 对验证队列进行分析,结果显示 HSATI、HSATII、LINE1-P1 和 Charlie 3 在 DNA 水平而非 RNA 水平上的代表性过高,接收者操作特征(ROC)曲线下面积(AUC)≥0.90。HSATI 和 HSATII DNA 与通过沉淀和大小排阻层析制备的 EV 共纯化,但不与外泌体免疫捕获共纯化,提示其在非外泌体复合物中包装。EV 相关重复元件 DNA 序列的一致过表达表明它们可能作为 OS 甚至其他癌症的生物标志物具有潜在的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf21/7794510/9405895d7631/41598_2020_77398_Fig1_HTML.jpg

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