MS CETSA deep functional proteomics uncovers DNA repair programs leading to gemcitabine resistance

Mechanisms for resistance to cytotoxic cancer drugs are dependent on dynamic changes in the biochemistry of cellular pathways, information which is hard to obtain at the systems level. Here we use a deep functional proteomics implementation of the Cellular Thermal Shift Assay to reveal a range of induced biochemical responses to gemcitabine in resistant and sensitive diffuse large B cell lymphoma cell lines. Initial responses in both, gemcitabine resistant and sensitive cells, reflect known targeted effects by gemcitabine on ribonucleotide reductase and DNA damage responses. However, later responses diverge dramatically where sensitive cells show induction of characteristic CETSA signals for early apoptosis, while resistant cells reveal biochemical modulations reflecting transition through a distinct DNA-damage signaling state, including opening of cell cycle checkpoints and induction of translesion DNA synthesis programs, allowing bypass of damaged DNA-adducts. The results also show the induction of a protein ensemble, labeled the Auxiliary DNA Damage Repair, likely supporting DNA replication at damaged sites that can be attenuated in resistant cells by an ATR inhibitor, thus re-establishing gemcitabine sensitivity and demonstrating ATR as a key signaling node of this response.

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Publication Details

Journal
Nature Communications
Published
2025-05-07
DOI
https://doi.org/10.1038/s41467-025-59505-8
Citations
2
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
1.61

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MS CETSA deep functional proteomics uncovers DNA repair programs leading to gemcitabine resistance

Anand D. Jeyasekharan, Jane Jia Hui Lee, Nayana Prabhu, Jiawen Lyu et al.
2 citations
Nature Communications
DNA Repair Mechanisms
1.61
article

MS CETSA deep functional proteomics uncovers DNA repair programs leading to gemcitabine resistance

Anand D. Jeyasekharan, Jane Jia Hui Lee, Nayana Prabhu, Jiawen Lyu, P. Nordlund, Hui Min Vivian Teo, Hai Van Le, Wai Leong Tam, Ying Liang, Marc-Antoine Gerault, Allison Chan, Khalidah Khalid, Mindaugas Raitelaitis
article en
2 citations

Abstract

Mechanisms for resistance to cytotoxic cancer drugs are dependent on dynamic changes in the biochemistry of cellular pathways, information which is hard to obtain at the systems level. Here we use a deep functional proteomics implementation of the Cellular Thermal Shift Assay to reveal a range of induced biochemical responses to gemcitabine in resistant and sensitive diffuse large B cell lymphoma cell lines. Initial responses in both, gemcitabine resistant and sensitive cells, reflect known targeted effects by gemcitabine on ribonucleotide reductase and DNA damage responses. However, later responses diverge dramatically where sensitive cells show induction of characteristic CETSA signals for early apoptosis, while resistant cells reveal biochemical modulations reflecting transition through a distinct DNA-damage signaling state, including opening of cell cycle checkpoints and induction of translesion DNA synthesis programs, allowing bypass of damaged DNA-adducts. The results also show the induction of a protein ensemble, labeled the Auxiliary DNA Damage Repair, likely supporting DNA replication at damaged sites that can be attenuated in resistant cells by an ATR inhibitor, thus re-establishing gemcitabine sensitivity and demonstrating ATR as a key signaling node of this response.

Nature CommunicationsVol. 16(1)
Agency for Science, Technology and Research (SG), National University of Singapore (SG), Karolinska Institutet (SE), National University Cancer Institute, Singapore (SG), Institute of Molecular and Cell Biology (RU), National Cancer Centre Singapore (SG), Genome Institute of Singapore (SG), Institute of Molecular and Cell Biology (SG)
National Research Foundation, Agency for Science, Technology and Research, National Research Foundation Singapore, Ministry of Education - Singapore, Cancerfonden, Karolinska Institutet, Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet, Medical Research Council, National Medical Research Council
Good health and well-being
Openalex Percentile: Top 17%
DNA Repair Mechanisms
1.61
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