Laser-Enhanced Assay Boosts Sensitivity for Colorectal Cancer Biomarker Detection

By LabMedica International staff writers
Posted on 30 Sep 2026

Colorectal cancer is the third most commonly diagnosed cancer and the second leading cause of cancer-related death worldwide. Early detection remains critical, but cancer biomarkers can produce only faint signals in blood samples, while conventional blood-based tests may require lengthy preparation and have limited sensitivity at very low concentrations. Researchers have now developed a laser-powered approach designed to enable faster detection of a colorectal cancer biomarker.

Researchers at Osaka Metropolitan University developed the approach using a microflow-type Light-induced Acceleration System (LAC-SYS) for rapid and sensitive biomarker detection. The technology is designed to detect glycoprotein CEACAM-5, a biomarker associated with colorectal cancer. The study was published in Nanoscale Horizons on June 29, 2026.


Image: Antibody-coated microscopic beads are introduced into a tiny flow channel containing blood plasma. Laser irradiation enhances their interaction with CEACAM-5, a colorectal cancer biomarker, causing the beads to assemble and generate a detectable signal. (Image Credit: Figure reproduced from Iida et al., Nanoscale Horizons(2026), DOI: 10.1039/d6nh00017g. Licensed under CC BY-NC 4.0.)

The method uses microscopic beads coated with multiple antibodies, which are introduced into a small flow channel containing blood plasma. When the sample is exposed to laser irradiation, LAC-SYS enhances interactions between the antibody-coated beads and CEACAM-5, causing the beads to assemble and produce a measurable signal.

The researchers tested the system using diluted blood plasma samples. For each experiment, 5 µL of plasma was serially diluted, with 1,000-fold diluted samples used primarily for patients with colorectal cancer. The method detected CEACAM-5 at concentrations of 1–10 picograms per milliliter in diluted plasma, representing a potential sensitivity improvement of one to two orders of magnitude compared with conventional immunoassays such as enzyme-linked immunosorbent assays and immunoprecipitation.

Further analysis showed that CEACAM-5 exists in blood as nanoscale aggregates. These clusters may interact efficiently with the antibody-coated beads, promoting bead assembly and strengthening the resulting detection signal. Based on this mechanism, the researchers said the technology could potentially be adapted to other disease-related biomarkers, including those associated with dementia and infectious diseases.

The next step is to validate the technology in clinical settings and determine how reliably it can distinguish disease-related signals in patient samples. The team also plans to work with industry partners to develop practical, portable diagnostic systems for broader use.

“Ultimately, our goal is to establish a rapid, highly sensitive, and minimally invasive platform for liquid biopsy and other blood-based diagnostic technologies that can support earlier disease detection and intervention,” said Takuya Iida, professor at the Graduate School of Science and Research Institute for LAC-SYS (RILACS) at Osaka Metropolitan University and lead author of this study.

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