# Diagnostic value of multi-gene methylation in colorectal cancer screening

**Authors:** Qingyan Yang, Liming Chen

PMC · DOI: 10.3389/fonc.2025.1660035 · Frontiers in Oncology · 2026-01-09

## TL;DR

This study shows that a multi-gene methylation test can accurately detect colorectal cancer and distinguish it from healthy individuals and polyps.

## Contribution

The study demonstrates the superior diagnostic accuracy of a six-gene methylation panel for colorectal cancer detection.

## Key findings

- The multi-gene methylation assay effectively differentiated CRC patients from healthy controls and polyp patients.
- The combined panel achieved an AUC of 0.958 in the training cohort and 0.952 in the validation cohort.
- Tumor size and TNM stage were identified as independent predictors of methylation positivity.

## Abstract

To evaluate the diagnostic value and clinical application of multi-gene methylation assay in colorectal cancer (CRC) screening.

This was a single-center, retrospective, real-world study conducted at the First Affiliated Hospital of Shantou University Medical College, China. A total of 450 participants were enrolled from January 2023 to December 2024, including 150 healthy individuals, 120 colorectal polyp patients, and 180 CRC patients. The methylation status of six plasma-derived loci (SEPT9-R1, SEPT9-R2, BCAT1, IKZF1, BCAN, and VAV3) was assessed using real-time multiplex quantitative PCR (qPCR). The diagnostic performance and predictive factors of the multi-gene methylation assay for CRC detection were assessed.

The multi-gene methylation assay effectively differentiated healthy controls, colorectal polyp patients, and CRC patients (P < 0.001), and methylation levels increased with advancing tumor stage. The combined panel demonstrated superior diagnostic accuracy over single-gene assays, yielding an AUC of 0.958 (95% CI: 0.934–0.982) in the training cohort and 0.952 (95% CI: 0.920–0.984) in the validation cohort. Multivariate analysis further identified tumor size (OR = 1.974, 95% CI: 1.321–2.950, P = 0.005) and TNM stage (OR = 2.117, 95% CI: 1.452–3.087, P = 0.002) as independent predictors of multi-gene methylation positivity.

Multi-gene methylation detection showed high diagnostic value for CRC and may serve as a valuable adjunct tool in CRC screening strategies.

## Linked entities

- **Genes:** BCAT1 (branched chain amino acid transaminase 1) [NCBI Gene 586], IKZF1 (IKAROS family zinc finger 1) [NCBI Gene 10320], BCAN (brevican) [NCBI Gene 63827], VAV3 (vav guanine nucleotide exchange factor 3) [NCBI Gene 10451]
- **Diseases:** colorectal cancer (MONDO:0005575), colorectal polyp (MONDO:0021392)

## Full-text entities

- **Genes:** BCAN (brevican) [NCBI Gene 63827] {aka BEHAB, CSPG7}, IKZF1 (IKAROS family zinc finger 1) [NCBI Gene 10320] {aka CVID13, Hs.54452, IK1, IKAROS, LYF1, LyF-1}, SEPTIN9 (septin 9) [NCBI Gene 10801] {aka AF17q25, MSF, MSF1, PNUTL4, SEPT9, SINT1}, BCAT1 (branched chain amino acid transaminase 1) [NCBI Gene 586] {aka BCATC, BCT1, ECA39, MECA39, PNAS121, PP18}, VAV3 (vav guanine nucleotide exchange factor 3) [NCBI Gene 10451]
- **Diseases:** CRC (MESH:D015179), colorectal polyp (MESH:D003111), tumor (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827121/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12827121/full.md

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Source: https://tomesphere.com/paper/PMC12827121