PARP inhibition increases sensitivity to cisplatin in non-small-cell lung carcinoma via the induction of TET-dependent hydroxymethylation

The improved response to cisplatin following PARPi-mediated sensitization of A549 cells, accompanied by the restoration of 5hmC levels, provides additional insights into the epigenetic mechanisms underlying the synergy between PARPi and cisplatin. The use of PARPi in clinical settings could increase the number of patients enriched in 5hmC, who might benefit from platinum-based therapy. Additionally, targeting epigenetic marks could provide a molecular basis for personalized cancer therapy directed to overcome tumor resistance.

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Publication Details

Journal
Frontiers in Cell and Developmental Biology
Published
2025-10-24
DOI
https://doi.org/10.3389/fcell.2025.1677261
Citations
1
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
1.05
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article

PARP inhibition increases sensitivity to cisplatin in non-small-cell lung carcinoma via the induction of TET-dependent hydroxymethylation

Jovana Rajić, Marijana Stojanović, Tijana Markovic, Nevena Grdović et al.
1 citations
Frontiers in Cell and Developmental Biology
PARP inhibition in cancer therapy
1.05
article

PARP inhibition increases sensitivity to cisplatin in non-small-cell lung carcinoma via the induction of TET-dependent hydroxymethylation

Jovana Rajić, Marijana Stojanović, Tijana Markovic, Nevena Grdović, Svetlana Dinić, Mirjana Mihailović, Ana Podolski-Renić, Stefan Hadžić, Melita Vidaković, Milica Pešić, Anja Tolić, Aleksandra Uskoković, Mirna Jovanović, Jelena Arambašić Јovanović, Marija Đorđević, Ana Šarić
article en
1 citations

Abstract

The improved response to cisplatin following PARPi-mediated sensitization of A549 cells, accompanied by the restoration of 5hmC levels, provides additional insights into the epigenetic mechanisms underlying the synergy between PARPi and cisplatin. The use of PARPi in clinical settings could increase the number of patients enriched in 5hmC, who might benefit from platinum-based therapy. Additionally, targeting epigenetic marks could provide a molecular basis for personalized cancer therapy directed to overcome tumor resistance.

Frontiers in Cell and Developmental BiologyVol. 13
University of Belgrade (RS), Institute of Physics Belgrade (RS)
Openalex Percentile: Top 17%
PARP inhibition in cancer therapy
1.05
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PARP inhibition increases sensitivity to cisplatin in non-small-cell lung carcinoma via the induction of TET-dependent hydroxymethylation — Jovana Rajić, Marijana Stojanović, et al. · Frontiers in Cell and Developmental Biology (2025) | TGRS Research Map | TGRS