A comprehensive survey of the mutagenic impact of common cancer cytotoxics

DSpace/Manakin Repository

A comprehensive survey of the mutagenic impact of common cancer cytotoxics

Citable link to this page

 

 
Title: A comprehensive survey of the mutagenic impact of common cancer cytotoxics
Author: Szikriszt, Bernadett; Póti, Ádám; Pipek, Orsolya; Krzystanek, Marcin; Kanu, Nnennaya; Molnár, János; Ribli, Dezső; Szeltner, Zoltán; Tusnády, Gábor E.; Csabai, István; Szallasi, Zoltan; Swanton, Charles; Szüts, Dávid

Note: Order does not necessarily reflect citation order of authors.

Citation: Szikriszt, B., Á. Póti, O. Pipek, M. Krzystanek, N. Kanu, J. Molnár, D. Ribli, et al. 2016. “A comprehensive survey of the mutagenic impact of common cancer cytotoxics.” Genome Biology 17 (1): 99. doi:10.1186/s13059-016-0963-7. http://dx.doi.org/10.1186/s13059-016-0963-7.
Full Text & Related Files:
Abstract: Background: Genomic mutations caused by cytotoxic agents used in cancer chemotherapy may cause secondary malignancies as well as contribute to the evolution of treatment-resistant tumour cells. The stable diploid genome of the chicken DT40 lymphoblast cell line, an established DNA repair model system, is well suited to accurately assay genomic mutations. Results: We use whole genome sequencing of multiple DT40 clones to determine the mutagenic effect of eight common cytotoxics used for the treatment of millions of patients worldwide. We determine the spontaneous mutagenesis rate at 2.3 × 10–10 per base per cell division and find that cisplatin, cyclophosphamide and etoposide induce extra base substitutions with distinct spectra. After four cycles of exposure, cisplatin induces 0.8 mutations per Mb, equivalent to the median mutational burden in common leukaemias. Cisplatin-induced mutations, including short insertions and deletions, are mainly located at sites of putative intrastrand crosslinks. We find two of the newly defined cisplatin-specific mutation types as causes of the reversion of BRCA2 mutations in emerging cisplatin-resistant tumours or cell clones. Gemcitabine, 5-fluorouracil, hydroxyurea, doxorubicin and paclitaxel have no measurable mutagenic effect. The cisplatin-induced mutation spectrum shows good correlation with cancer mutation signatures attributed to smoking and other sources of guanine-directed base damage. Conclusion: This study provides support for the use of cell line mutagenesis assays to validate or predict the mutagenic effect of environmental and iatrogenic exposures. Our results suggest genetic reversion due to cisplatin-induced mutations as a distinct mechanism for developing resistance. Electronic supplementary material The online version of this article (doi:10.1186/s13059-016-0963-7) contains supplementary material, which is available to authorized users.
Published Version: doi:10.1186/s13059-016-0963-7
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862131/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:27320271
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)

 
 

Search DASH


Advanced Search
 
 

Submitters