Aug 2026· Epigenomics· pp.
1-9
· 0 citations· 61 references
Medicine
TL;DR
It is proposed that incorporating epigenetic information may refine prognostic assessment, while emphasizing the need for rigorous validation prior to clinical implementation.
Abstract
Accurate prognostic stratification remains a major challenge in colorectal cancer (CRC), as substantial heterogeneity in clinical outcomes persists even within the same pathological stage. While mutation-based circulating tumor DNA (ctDNA) analysis has transformed postoperative risk assessment by enabling detection of molecular residual disease (MRD), it primarily reflects the presence of tumor-derived genetic alterations and may not fully capture the biological processes underlying tumor progression. DNA methylation represents a complementary molecular layer that reflects coordinated regulatory states associated with tumor behavior, including transcriptional programs and cellular plasticity. Recent studies suggest that ctDNA methylation profiling may provide additional prognostic information beyond conventional clinicopathological factors and mutation-based assays, particularly in early-stage and postoperative settings. However, important challenges remain, including assay heterogeneity, lack of standardized metrics, and the need for robust external validation. In this Perspective, we examine the limitations of current prognostic frameworks and discuss the potential role of ctDNA methylation analysis as part of an integrated, multidimensional model for risk stratification in CRC. We propose that incorporating epigenetic information may refine prognostic assessment, while emphasizing the need for rigorous validation prior to clinical implementation.
Background Stage II colon cancer is clinically heterogeneous. Current clinicopathologic risk factors cannot accurately identify patients with residual disease after curative resection. Circulating tumor DNA (ctDNA) has emerged as a promising biomarker for the detection of minimal residual disease (MRD), defined as micr...
Er-Hua Yang, Xue-Feng Wang, Jia-Jing Zhang et al.· Frontiers in Oncology· 0 citations
The biological and clinical relevance of the epigenetic landscape of cfDNA in LC patients is explored, particularly focusing on DNA methylation-based biomarkers and their evolving applications towards early diagnosis and post-surgical monitoring of minimal residual disease (MRD).
T. D. Bazan Russo, V. Gristina, M. D. Delcuratolo et al.· Frontiers in Oncology· 0 citations
Continuous technological innovation, prospective multicenter validation, standardized testing protocols, and evidence-based clinical guidelines are essential to fully integrate ctDNA into routine precision breast cancer care.
E. I. Obeagu, C. Okafor· Breast Cancer: Basic and Cli...· 0 citations
Although the clinical utility of the TMBRS is currently moderate, this research provides a critical proof of concept for the interplay among PTGS2, mutational load, and the tumor microenvironment, offering valuable mechanistic insights for future large-scale prospective clinical trials.
Batchimeg Tsedenbal, B. Chimeddorj, Shu-Tao Tan et al.· Eurasian Journal of Medicine...· 0 citations
Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related death worldwide, owing to late-stage diagnosis and underlying liver disease that limits curative treatment options. Conventional surveillance and diagnostic strategies relying on imaging and alpha-fetoprotein (AFP) lack sufficient sensitivity, par...
M. Amer, Valeria Tosello, Elisa Pinto· International Journal of Bio...· 0 citations
The findings suggest that tumor-informed ctDNA analysis provides a promising approach for post-operative MRD surveillance and recurrence risk stratification in CRC, however, the small sample size, lack of external validation, and absence of neoadjuvant-treated patients preclude definitive conclusions.
William C. Cho, Yingyu Wang, Qian-Qian Yao et al.· Oncology Research· 0 citations
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