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Comparing genotoxic signatures in cord blood cells from neonates exposed in utero to zidovudine or tenofovir.

cancer

HIV

stem cell

Authors: Alexandre A. Vivanti, Tayebeh S TS. Soheili, Wendy W. Cuccuini, Sonia S. Luce, Laurent L. Mandelbrot, Jerome J. Lechenadec, Anne-Gael AG. Cordier, Elie E. Azria, Jean J. Soulier, Marina M. Cavazzana, Stéphane S. Blanche, Isabelle I. André-Schmutz
Published: 06/23/2015, AIDS (London, England)

Objectives

Zidovudine and tenofovir are the two main nucleos(t)ide analogs used to prevent mother-to-child transmission of HIV. In vitro, both drugs bind to and integrate into human DNA and inhibit telomerase. The objective of the present study was to assess the genotoxic effects of either zidovudine or tenofovir-based combination therapies on cord blood cells in newborns exposed in utero.

Design

We compared the aneuploid rate and the gene expression profiles in cord blood samples from newborns exposed either to zidovudine or tenofovir-based combination therapies during pregnancy and from unexposed controls (n = 8, 9, and 8, respectively).

Methods

The aneuploidy rate was measured on the cord blood T-cell karyotype. Gene expression profiles of cord blood T cells and hematopoietic stem and progenitor cells were determined with microarrays, analyzed in a gene set enrichment analysis and confirmed by real-time quantitative PCRs.

Results

Aneuploidy was more frequent in the zidovudine-exposed group (26.3%) than in the tenofovir-exposed group (14.2%) or in controls (13.3%; P < 0.05 for both). The transcription of genes involved in DNA repair, telomere maintenance, nucleotide metabolism, DNA/RNA synthesis, and the cell cycle was deregulated in samples from both the zidovudine and the tenofovir-exposed groups.

Conclusion

Although tenofovir has a lower clastogenic impact than zidovudine, gene expression profiling showed that both drugs alter the transcription of DNA repair and telomere maintenance genes.

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