The Origin of Highly Elevated Cell-Free DNA in Healthy Individuals and Patients with Pancreatic, Colorectal, Lung, or Ovarian Cancer

Author:

Mattox Austin K.1234ORCID,Douville Christopher1234ORCID,Wang Yuxuan1234ORCID,Popoli Maria123ORCID,Ptak Janine1234ORCID,Silliman Natalie1234ORCID,Dobbyn Lisa123ORCID,Schaefer Joy1234ORCID,Lu Steve1234ORCID,Pearlman Alexander H.1234ORCID,Cohen Joshua D.1234ORCID,Tie Jeanne567ORCID,Gibbs Peter567ORCID,Lahouel Kamel8ORCID,Bettegowda Chetan1239ORCID,Hruban Ralph H.10ORCID,Tomasetti Cristian8ORCID,Jiang Peiyong1112ORCID,Chan K.C. Allen1112ORCID,Lo Yuk Ming Dennis1112ORCID,Papadopoulos Nickolas123ORCID,Kinzler Kenneth W.123ORCID,Vogelstein Bert1234ORCID

Affiliation:

1. 1Ludwig Center for Cancer Genetics and Therapeutics, Johns Hopkins University School of Medicine, Baltimore, Maryland.

2. 2Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.

3. 3The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.

4. 4Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

5. 5Division of Systems Biology and Personalized Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.

6. 6Department of Medical Oncology, Western Health, St Albans, Victoria, Australia.

7. 7Department of Medical Oncology, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Parkville, Victoria, Australia.

8. 8Division of Mathematics for Cancer Evolution and Early Detection, Department of Computational and Quantitative Medicine, Beckman Research Institute, City of Hope National Medical Center, Duarte, California.

9. 9Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.

10. 10Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins Medical Institutions, Johns Hopkins University, Baltimore, Maryland.

11. 11State Key Laboratory of Translational Oncology and Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong SAR, China.

12. 12Centre for Novostics, Hong Kong Science Park, Pak Shek Kok, New Territories, Hong Kong SAR, China.

Abstract

Abstract Cell-free DNA (cfDNA) concentrations from patients with cancer are often elevated compared with those of healthy controls, but the sources of this extra cfDNA have never been determined. To address this issue, we assessed cfDNA methylation patterns in 178 patients with cancers of the colon, pancreas, lung, or ovary and 64 patients without cancer. Eighty-three of these individuals had cfDNA concentrations much greater than those generally observed in healthy subjects. The major contributor of cfDNA in all samples was leukocytes, accounting for ∼76% of cfDNA, with neutrophils predominating. This was true regardless of whether the samples were derived from patients with cancer or the total plasma cfDNA concentration. High levels of cfDNA observed in patients with cancer did not come from either neoplastic cells or surrounding normal epithelial cells from the tumor's tissue of origin. These data suggest that cancers may have a systemic effect on cell turnover or DNA clearance. Significance: The origin of excess cfDNA in patients with cancer is unknown. Using cfDNA methylation patterns, we determined that neither the tumor nor the surrounding normal tissue contributes this excess cfDNA—rather it comes from leukocytes. This finding suggests that cancers have a systemic impact on cell turnover or DNA clearance. See related commentary by Thierry and Pisareva, p. 2122. This article is featured in Selected Articles from This Issue, p. 2109

Funder

Lustgarden Foundation for Pancreatic Cancer Research

The Virginia and DK Ludwig Fund for Cancer Research

The Sol Goldman Center for Pancreatic Cancer Research

Marcus Foundation

John Templeton Foundation

National Institutes of Health

Hong Kong Research Grants Council Theme-Based Research Grant

Innovation and Technology Commission of the Hong Kong SAR Government

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology

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