Abnormal epigenetic aging of epigenetic outliers in normal colon mucosa from colorectal cancer patients

A subset of colorectal cancer (CRC) patients displays abnormal DNA methylation patterns (“Outlier Methylation Phenotype” (OMP)) in normal adjacent tissue (NAT). We analyzed the impact of OMP status on epigenetic age and tumor progression using published aging and mitotic clocks and colonic epigenetic clock (EpiAge) developed on controls, with equal representation from Black and Caucasian populations. Three aging clocks (including EpiAge) showed “significantly lower” epigenetic age in CRC. Mitotic clocks suggested significantly fewer stem cell divisions in CRC versus controls. A binomial model using inactive X chromosome CpGs suggested that NAT of CRC patients had fewer stem cells compared with controls. On comparing NAT and tumor methylome, the OMP group showed the fewest epigenetic differences. In conclusion, our study demonstrates that NAT of OMP-CRC patients undergoes epigenetic age deceleration and have fewer epigenetic differences with tumor tissues, suggesting that NAT of OMPs had progressed toward a tumor identity.

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Journal
Scientific Reports
Published
2026-01-07
DOI
https://doi.org/10.1038/s41598-025-34035-x
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00

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article

Abnormal epigenetic aging of epigenetic outliers in normal colon mucosa from colorectal cancer patients

Bryant M. Schultz, Stanley Basickes, Jayashri Ghosh, Carmen Sapienza et al.
Scientific Reports
Epigenetics and DNA Methylation
article

Abnormal epigenetic aging of epigenetic outliers in normal colon mucosa from colorectal cancer patients

Bryant M. Schultz, Stanley Basickes, Jayashri Ghosh, Carmen Sapienza, Juie Nahushkumar Rana, Olorunfemi Ayeotan, Samuel Litwin
article en

Abstract

A subset of colorectal cancer (CRC) patients displays abnormal DNA methylation patterns (“Outlier Methylation Phenotype” (OMP)) in normal adjacent tissue (NAT). We analyzed the impact of OMP status on epigenetic age and tumor progression using published aging and mitotic clocks and colonic epigenetic clock (EpiAge) developed on controls, with equal representation from Black and Caucasian populations. Three aging clocks (including EpiAge) showed “significantly lower” epigenetic age in CRC. Mitotic clocks suggested significantly fewer stem cell divisions in CRC versus controls. A binomial model using inactive X chromosome CpGs suggested that NAT of CRC patients had fewer stem cells compared with controls. On comparing NAT and tumor methylome, the OMP group showed the fewest epigenetic differences. In conclusion, our study demonstrates that NAT of OMP-CRC patients undergoes epigenetic age deceleration and have fewer epigenetic differences with tumor tissues, suggesting that NAT of OMPs had progressed toward a tumor identity.

Scientific ReportsVol. 16(1)
Fox Chase Cancer Center (US), Greenfield Community College (US), Temple University Health System (US), Temple University (US)
National Cancer Institute
Good health and well-being
Openalex Percentile: Top 96%
Epigenetics and DNA Methylation
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Abnormal epigenetic aging of epigenetic outliers in normal colon mucosa from colorectal cancer patients — Bryant M. Schultz, Stanley Basickes, et al. · Scientific Reports (2026) | TGRS Research Map | TGRS