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Updated: Feb 6, 2026

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Determination of In Vitro and Cellular Turn-on Kinetics for Fluorogenic RNA Aptamers
Published on: August 9, 2022
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CRISPR/Cas13a-Engineered RNA-Based Fluorogenic Biosensor for Label-Free Quantification of RNA in Colorectal Tissues
Yu-Chen Xu1, Wen-Jing Liu1, Chen-Chen Li2
1School of Chemistry and Chemical Engineering, State Key Laboratory of Digital Medical Engineering, Southeast University, Nanjing 211189, China.
Analytical Chemistry
|February 5, 2026
Summary
A novel RNA biosensor detects BRD2 RNA, a potential biomarker for early colorectal cancer (CRC) diagnosis. This CRISPR/Cas13a-based tool offers sensitive, label-free detection in patient tissues, paving the way for improved diagnostics.
Area of Science:
- Biomolecular Engineering
- Molecular Diagnostics
- Cancer Research
Background:
- Colorectal cancer (CRC) poses a significant global health challenge, with early diagnosis remaining difficult.
- Identifying reliable noninvasive biomarkers is crucial for effective CRC detection and management.
Purpose of the Study:
- To develop a sensitive and specific RNA-based biosensor for detecting BRD2 RNA as a biomarker for colorectal cancer.
- To establish a label-free detection method for BRD2 RNA in colorectal tissues using CRISPR/Cas13a technology.
Main Methods:
- Construction of a CRISPR/Cas13a-engineered RNA-based fluorogenic biosensor for BRD2 RNA detection.
- Utilizing Cas13a's trans-cleavage activity and transcription amplification for signal generation.
- Employing Pepper RNA aptamers and a fluorophore (HBC620) for sensitive signal readout.
Main Results:
- The biosensor achieved highly sensitive detection of BRD2 RNA down to 0.39 fM.
- Accurate quantification of BRD2 RNA expression at the single-cell level was demonstrated.
- The biosensor successfully distinguished between colorectal cancer patient tissues and adjacent normal tissues.
Conclusions:
- BRD2 RNA is a promising noninvasive biomarker for colorectal cancer.
- The developed CRISPR/Cas13a-based fluorogenic biosensor provides a sensitive and adaptable platform for early cancer diagnostics.
- The programmability of the biosensor allows for potential adaptation to detect other RNA targets, including noncoding and viral RNAs.
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