Cell-Free DNA 5-Hydroxymethylcytosine Signatures for Lung Cancer Prognosis

Author:

Shao Jianming12,Olsen Randall J.123,Kasparian Saro45,He Chuan67,Bernicker Eric H.4,Li Zejuan123

Affiliation:

1. Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX 77030, USA

2. Houston Methodist Research Institute, Houston, TX 77030, USA

3. Weill Cornell Medical College, New York, NY 10065, USA

4. Cancer Center, Houston Methodist Hospital, Houston, TX 77030, USA

5. Department of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA

6. Department of Chemistry, Department of Biochemistry and Molecular Biology, Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA

7. Howard Hughes Medical Institute, The University of Chicago, Chicago, IL 60637, USA

Abstract

Accurate prognostic markers are essential for guiding effective lung cancer treatment strategies. The level of 5-hydroxymethylcytosine (5hmC) in tissue is independently associated with overall survival (OS) in lung cancer patients. We explored the prognostic value of cell-free DNA (cfDNA) 5hmC through genome-wide analysis of 5hmC in plasma samples from 97 lung cancer patients. In both training and validation sets, we discovered a cfDNA 5hmC signature significantly associated with OS in lung cancer patients. We built a 5hmC prognostic model and calculated the weighted predictive scores (wp-score) for each sample. Low wp-scores were significantly associated with longer OS compared to high wp-scores in the training [median 22.9 versus 8.2 months; p = 1.30 × 10−10; hazard ratio (HR) 0.04; 95% confidence interval (CI), 0.00–0.16] and validation (median 18.8 versus 5.2 months; p = 0.00059; HR 0.22; 95% CI: 0.09–0.57) sets. The 5hmC signature independently predicted prognosis and outperformed age, sex, smoking, and TNM stage for predicting lung cancer outcomes. Our findings reveal critical genes and signaling pathways with aberrant 5hmC levels, enhancing our understanding of lung cancer pathophysiology. The study underscores the potential of cfDNA 5hmC as a superior prognostic tool for guiding more personalized therapeutic strategies for lung cancer patients.

Funder

American Cancer Society

National Human Genome Research Institute

Publisher

MDPI AG

Subject

General Medicine

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