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[Cancer Research 61, 1659-1665, February 15, 2001]
© 2001 American Association for Cancer Research


Tumor Biology

DNA Fragments in the Blood Plasma of Cancer Patients: Quantitations and Evidence for Their Origin from Apoptotic and Necrotic Cells1

Sabine Jahr2, Hannes Hentze, Sabine Englisch, Dieter Hardt, Frank O. Fackelmayer, Rolf-Dieter Hesch and Rolf Knippers

Department of Biology [S. J., H. H., F. O. F., R. K.] and Steinbeis-Transfer-Laboratory for Biomolecular Medicine [S. E., R-D. H.], Universität Konstanz, D-78457 Konstanz, and Department of Oncology, Klinikum Konstanz [D. H.], D-78464, Konstanz, Germany

Increased levels of DNA fragments have frequently been found in the blood plasma of cancer patients. Published data suggest that only a fraction of the DNA in blood plasma is derived from cancer cells. However, it is not known how much of the circulating DNA is from cancer or from noncancer cells. By quantitative methylation-specific PCR of the promoter region of the CDKN2A tumor suppressor gene, we were able to quantify the fraction of plasma DNA derived from tumor cells. In the plasma samples of 30 unselected cancer patients, we detected quantities of tumor DNA from only 3% to as much as 93% of total circulating DNA. We investigated possible origins of nontumor DNA in the plasma and demonstrate here a contribution of T-cell DNA in a few cases only. To investigate the possibility that plasma DNA originates from apoptotic or necrotic cells, we performed studies with apoptotic (staurosporine) and necrotic (staurosporine plus oligomycin) cells in vitro and with mice after induction of apoptotic (anti-CD95) or necrotic (acetaminophen) liver injury. Increasing amounts of DNA were found to be released in the supernatants of cells and in the blood plasma samples of treated animals. A clear discrimination of apoptotic and necrotic plasma DNA was possible by gel electrophoresis. The same characteristic patterns of DNA fragments could be identified in plasma derived from different cancer patients. The data are consistent with the possibility that apoptotic and necrotic cells are a major source for plasma DNA in cancer patients.




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Clin. Cancer Res.Home page
H.-W. Chang, S. Z. Ali, S. K. R. Cho, R. J. Kurman, and I.-M. Shih
Detection of Allelic Imbalance in Ascitic Supernatant by Digital Single Nucleotide Polymorphism Analysis
Clin. Cancer Res., August 1, 2002; 8(8): 2580 - 2585.
[Abstract] [Full Text] [PDF]


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Toxicol SciHome page
J. S. Gujral, T. R. Knight, A. Farhood, M. L. Bajt, and H. Jaeschke
Mode of Cell Death after Acetaminophen Overdose in Mice: Apoptosis or Oncotic Necrosis?
Toxicol. Sci., June 1, 2002; 67(2): 322 - 328.
[Abstract] [Full Text] [PDF]


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Clin. Cancer Res.Home page
H.-Z. Zou, B.-M. Yu, Z.-W. Wang, J.-Y. Sun, H. Cang, F. Gao, D. H. Li, R. Zhao, G.-G. Feng, and J. Yi
Detection of Aberrant p16 Methylation in the Serum of Colorectal Cancer Patients
Clin. Cancer Res., January 1, 2002; 8(1): 188 - 191.
[Abstract] [Full Text] [PDF]


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Clin. Chem.Home page
R. W. K. Chiu, L. L. M. Poon, T. K. Lau, T. N. Leung, E. M. C. Wong, and Y. M. D. Lo
Effects of Blood-Processing Protocols on Fetal and Total DNA Quantification in Maternal Plasma
Clin. Chem., September 1, 2001; 47(9): 1607 - 1613.
[Abstract] [Full Text] [PDF]


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Clin. Chem.Home page
D. O. Hasselmann, G. Rappl, W. Tilgen, and U. Reinhold
Extracellular Tyrosinase mRNA within Apoptotic Bodies Is Protected from Degradation in Human Serum
Clin. Chem., August 1, 2001; 47(8): 1488 - 1489.
[Full Text] [PDF]




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