Issue 8, 2023

An enzyme-powered microRNA discriminator for the subtype-specific diagnosis of breast cancer

Abstract

Breast cancer, a disease with highly heterogeneous features, is the most common malignancy diagnosed in people worldwide. Early diagnosis of breast cancer is crucial for improving its cure rate, and accurate classification of the subtype-specific features is essential to precisely treat the disease. An enzyme-powered microRNA (miRNA, RNA = ribonucleic acid) discriminator was developed to selectively distinguish breast cancer cells from normal cells and further identify subtype-specific features. Specifically, miR-21 was used as a universal biomarker to discriminate between breast cancer cells and normal cells, and miR-210 was used to identify triple-negative subtype features. The experimental results demonstrated that the enzyme-powered miRNA discriminator displayed low limits of detection at fM levels for both miR-21 and miR-210. Moreover, the miRNA discriminator enabled the discrimination and quantitative determination of breast cancer cells derived from different subtypes based on their miR-21 levels, and the further identification of the triple-negative subtype in combination with the miR-210 levels. Therefore, it is hoped that this study will provide insight into subtype-specific miRNA profiling, which may have potential use in the clinical management of breast tumours based on their subtype characteristics.

Graphical abstract: An enzyme-powered microRNA discriminator for the subtype-specific diagnosis of breast cancer

Supplementary files

Article information

Article type
Edge Article
Submitted
06 Jan 2023
Accepted
26 Jan 2023
First published
31 Jan 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 2097-2106

An enzyme-powered microRNA discriminator for the subtype-specific diagnosis of breast cancer

H. Mao, Y. Cao, Z. Zou, J. Xia and J. Zhao, Chem. Sci., 2023, 14, 2097 DOI: 10.1039/D3SC00090G

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