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通过信号探针杂交实现血清微小RNA的无PCR和无洗涤检测。

PCR- and wash-free detection of serum miRNA via signaling probe hybridization.

作者信息

Uno Haruka, Takeuchi Hiyori, Abe Ishin, Yoshino Tomoko, Taguchi Tomoyuki, Hirakawa Yuko, Matsunaga Tadashi, Tanaka Tsuyoshi

机构信息

Division of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, Tokyo, Japan.

Yokogawa Electric Corporation, Tokyo, Japan.

出版信息

Biotechnol Bioeng. 2025 Jan;122(1):159-166. doi: 10.1002/bit.28859. Epub 2024 Oct 13.

Abstract

Detection of microRNAs (miRNAs) in the serum is an effective liquid biopsy technique for cancer diagnosis. However, conventional diagnostic methods are time-consuming and complex. Therefore, in this study, we established a signaling probe-based DNA microarray system for miRNA detection. PCR, fluorescence labeling, and washing are not necessary for signaling probes. Four probes were designed using different miRNAs as diagnostic cancer markers. The developed system is useful for various miRNAs, regardless of their target lengths (18-26-mer) and GC content (36%-89%). Here, all the assays were performed within 40 min. Overall, our signaling probe-based DNA hybridization system facilitates the simple and rapid detection of serum miRNAs without the need for gene amplification, fluorescence labeling and washing.

摘要

血清中微小RNA(miRNA)的检测是一种用于癌症诊断的有效液体活检技术。然而,传统的诊断方法既耗时又复杂。因此,在本研究中,我们建立了一种基于信号探针的DNA微阵列系统用于miRNA检测。信号探针不需要进行PCR、荧光标记和洗涤。使用不同的miRNA作为诊断癌症标志物设计了四种探针。所开发的系统适用于各种miRNA,无论其靶标长度(18 - 26个核苷酸)和GC含量(36% - 89%)如何。在此,所有检测均在40分钟内完成。总体而言,我们基于信号探针的DNA杂交系统有助于简单快速地检测血清miRNA,而无需基因扩增、荧光标记和洗涤。

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