4.7 Article

High-throughput quantitative detection of triple-negative breast cancer-associated expressed miRNAs by rolling circle amplification on fluorescence-encoded microspheres

Journal

CHINESE CHEMICAL LETTERS
Volume 34, Issue 9, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2023.108141

Keywords

MicroRNAs; Rolling circle amplification; Fluorescence -encoded microspheres; High -throughput; Triple -negative breast cancer

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Compared with other types of breast cancer, triple-negative breast cancer (TNBC) has a high degree of malignancy and poor prognosis. Early diagnosis of TNBC through specific miRNA expression profiles can reduce its mortality. In this study, we developed a high-throughput, high-sensitivity method for quantitatively detecting multiple sets of TNBC-associated miRNAs using rolling circle amplification on fluorescence-encoded microspheres. The method showed extensive linear dynamic range, high sensitivity, reasonable specificity, and good recovery and reproducibility in serum.
Compared with other types of breast cancer, triple-negative breast cancer (TNBC) has the characteristics of a high degree of malignancy and poor prognosis. Early diagnosis of TNBC through biological markers and timely development of effective treatment methods can reduce its mortality. Many Research experiments have confirmed that some specific miRNA expression profiles in TNBC can used as markers for early diagnosis. However, detecting the expression profiles of multiple groups of miRNAs according to traditional detection methods is complicated and consumes many samples. To address this issue, we developed a method for high-throughput, high-sensitivity quantitative detection of multiple sets of miRNAs (including miR-16, miR-21, miR-92, miR-199, and miR-342) specifically expressed in TNBC by rolling circle amplification (RCA) on fluorescence-encoded microspheres. Through the optimization of reaction system conditions, the developed method showed an extensive linear dynamic range and high sensitivity for all five miRNAs with the lowest limit of detection of 2 fmol/L. Meanwhile, this high-throughput detection method also appeared reasonable specificity. Only in the presence of a specific target miRNA, the fluorescence signal on the correspondingly encoded microspheres is significantly increased, while the fluorescence signal on other non-correspondingly encoded microspheres is almost negligible. Furthermore, this process exhibited good recovery and reproducibility in serum. The advantages of this method allow us to more conveniently obtain the expression profiles of multiple groups of TNBC-associated miRNAs, which is beneficial for the early detection of TNBC.& COPY; 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.

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