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Cited by 284

The DOI matches its Crossref record; 88 of the 88 references it cites were found in a registry or an index.

Cell-Free DNA and Apoptosis: How Dead Cells Inform About the Living

Heitzer, Ellen, Auinger, Lisa, Speicher, Michael R.·2020·Trends in Molecular Medicine

Abstract

Cell-free DNA (cfDNA) is evolving into a widely used prognostic and predictive biomarker, particularly in oncology. However, its versatile clinical use precedes a profound understanding of the underlying biology of cfDNA release. There is much evidence to suggest that cfDNA is mainly derived from dying (i.e., apoptotic) cells. However, numerous cancer studies have shown that cfDNA is informative about acquired resistance to given therapies, which is present in living, proliferating tumor subclones. To explain this contradiction, we review current insights regarding cfDNA release, in particular the interplay between apoptosis and proliferation. We describe how improved knowledge about cfDNA biology could be used for novel therapeutic strategies and how this may affect patient management.

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Metadata

Authors
Heitzer, E., Auinger, L., & Speicher, M. R.
Venue
Trends in Molecular Medicine
Publisher
Elsevier BV
Published
2020-05
Volume
26
Issue
5
Pages
519-528
ISSN
1471-4914 (ISSN-L)
OpenAlex
W3007237049
Cited by
284
References
88
FWCI
4.90
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Cell-Free DNA and Apoptosis: How Dead Cells Inform About the Living. https://app.cochat.ai/papers/10.1016/j.molmed.2020.01.012
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Heitzer, E., Auinger, L., & Speicher, M. R. (2020). Cell-Free DNA and Apoptosis: How Dead Cells Inform About the Living. Trends in Molecular Medicine. https://doi.org/10.1016/j.molmed.2020.01.012

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.