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Rebhandl S, Huemer M, Greil R, et al. AID/APOBEC deaminases and cancer. Oncoscience. 2015;2(4):320-33doi: 10.18632/oncoscience.155.
Rebhandl, S., Huemer, M., Greil, R., & Geisberger, R. (2015). AID/APOBEC deaminases and cancer. Oncoscience, 2(4), 320-33. https://doi.org/10.18632/oncoscience.155
Rebhandl, Stefan, et al. "AID/APOBEC deaminases and cancer." Oncoscience vol. 2,4 (2015): 320-33. doi: https://doi.org/10.18632/oncoscience.155
Rebhandl S, Huemer M, Greil R, Geisberger R. AID/APOBEC deaminases and cancer. Oncoscience. 2015 Apr 28;2(4):320-33. doi: 10.18632/oncoscience.155. eCollection 2015. PMID: 26097867; PMCID: PMC4468319.
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Oncoscience. 2015 Apr 28;2(4):320-33. doi: 10.18632/oncoscience.155. eCollection 2015.

AID/APOBEC deaminases and cancer.

Oncoscience

Stefan Rebhandl, Michael Huemer, Richard Greil, Roland Geisberger

Affiliations

  1. Department of internal Medicine III with Hematology, Medical Oncology, Hemostaseology, Infectious Diseases, Rheumatology, Oncologic Center, Laboratory for Immunological and Molecular Cancer Research, Paracelsus Medical University Salzburg, Austria ; Salzburg Cancer Research Institute, Salzburg, Austria.

PMID: 26097867 PMCID: PMC4468319 DOI: 10.18632/oncoscience.155

Abstract

Mutations are the basis for evolution and the development of genetic diseases. Especially in cancer, somatic mutations in oncogenes and tumor suppressor genes alongside the occurrence of passenger mutations have been observed by recent deep-sequencing approaches. While mutations have long been considered random events induced by DNA-replication errors or by DNA damaging agents, genome sequencing led to the discovery of non-random mutation signatures in many human cancer. Common non-random mutations comprise DNA strand-biased mutation showers and mutations restricted to certain DNA motifs, which recently have become attributed to the activity of the AID/APOBEC family of DNA deaminases. Hence, APOBEC enzymes, which have evolved as key players in natural and adaptive immunity, have been proposed to contribute to cancer development and clonal evolution of cancer by inducing collateral genomic damage due to their DNA deaminating activity. This review focuses on how mutagenic events through AID/APOBEC deaminases may contribute to cancer development.

Keywords: AID; APOBEC3; cancer; deamination; kataegis; mutation cluster; mutation signature

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