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通过纳米线揭示大量与癌症相关的尿 microRNA 候选物。

Unveiling massive numbers of cancer-related urinary-microRNA candidates via nanowires.

机构信息

Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.

ImPACT Research Center for Advanced Nanobiodevices, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.

出版信息

Sci Adv. 2017 Dec 15;3(12):e1701133. doi: 10.1126/sciadv.1701133. eCollection 2017 Dec.

DOI:10.1126/sciadv.1701133
PMID:29291244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5744465/
Abstract

Analyzing microRNAs (miRNAs) within urine extracellular vesicles (EVs) is important for realizing miRNA-based, simple, and noninvasive early disease diagnoses and timely medical checkups. However, the inherent difficulty in collecting dilute concentrations of EVs (<0.01 volume %) from urine has hindered the development of these diagnoses and medical checkups. We propose a device composed of nanowires anchored into a microfluidic substrate. This device enables EV collections at high efficiency and in situ extractions of various miRNAs of different sequences (around 1000 types) that significantly exceed the number of species being extracted by the conventional ultracentrifugation method. The mechanical stability of nanowires anchored into substrates during buffer flow and the electrostatic collection of EVs onto the nanowires are the two key mechanisms that ensure the success of the proposed device. In addition, we use our methodology to identify urinary miRNAs that could potentially serve as biomarkers for cancer not only for urologic malignancies (bladder and prostate) but also for nonurologic ones (lung, pancreas, and liver). The present device concept will provide a foundation for work toward the long-term goal of urine-based early diagnoses and medical checkups for cancer.

摘要

分析尿液细胞外囊泡(EVs)中的 microRNAs(miRNAs)对于实现基于 miRNA 的简单、非侵入性的早期疾病诊断和及时的医疗检查非常重要。然而,从尿液中收集稀释浓度的 EVs(<0.01 体积%)具有内在的困难,这阻碍了这些诊断和医疗检查的发展。我们提出了一种由纳米线锚定在微流控基底上组成的装置。该装置能够高效地收集 EVs,并原位提取各种不同序列的 miRNA(约 1000 种),这大大超过了传统超速离心法提取的物种数量。在缓冲液流动过程中纳米线锚定在基底上的机械稳定性和 EVs 静电收集到纳米线上是确保所提出的装置成功的两个关键机制。此外,我们使用我们的方法来鉴定尿液中的 miRNA,这些 miRNA 可能作为癌症的生物标志物,不仅对泌尿系统恶性肿瘤(膀胱和前列腺),而且对非泌尿系统恶性肿瘤(肺、胰腺和肝脏)也是如此。本装置概念将为基于尿液的癌症早期诊断和医疗检查的长期目标提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/d43c54eb637d/1701133-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/4fdd98f90ff6/1701133-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/2c6685825f13/1701133-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/b93462f692b4/1701133-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/0a1f9018f6e6/1701133-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/d43c54eb637d/1701133-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/4fdd98f90ff6/1701133-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/2c6685825f13/1701133-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/b93462f692b4/1701133-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/0a1f9018f6e6/1701133-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ee/5744465/d43c54eb637d/1701133-F5.jpg

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