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The effects of deregulated DNA damage signalling on cancer chemotherapy response and resistance
Abstract
Tumours with specific DNA repair defects can be completely dependent on back-up DNA repair pathways for their survival. This dependence can be exploited therapeutically to induce synthetic lethality in tumour cells. For instance, homologous recombination (HR)-deficient tumours can be effectively targeted by DNA double-strand break-inducing agents. However, not all HR-defective tumours respond equally well to this type of therapy. Tumour cells may acquire resistance by invoking biochemical mechanisms that reduce drug action or by acquiring additional alterations in DNA damage response pathways. A thorough understanding of these processes is important for predicting treatment response and for the development of novel treatment strategies that prevent the emergence of therapy-resistant tumours.
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“Defective DNA repair and DDR pathways may lead to several human diseases, such as cancer and neurodegenerative diseases [6, 33–38]”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [37]
In the citing paper
“Dysfunctions in these pathways are linked to cancer and neurodegenerative diseases [6, 33–38]”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [37]
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Metadata
- Authors
- Bouwman, P., & Jonkers, J.
- Affiliations
- The Netherlands Cancer Institute (NL)
- Corresponding author
- Jonkers, Jos
- Venue
- Nature Reviews Cancer
- Published
- 2012-08-24
- Volume
- 12
- Issue
- 9
- Pages
- 587-598
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W1980438635
- Cited by
- 615
- References
- 151
- Citations by year
- 2026: 20 · 2025: 31 · 2024: 43 · 2023: 40 · 2022: 52 · 2021: 47 · 2020: 56 · 2019: 29 · 2018: 46 · 2017: 56 · 2016: 52 · 2015: 43 · 2014: 53 · 2013: 44 · 2012: 3
- FWCI
- 4.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Commission
- KWF Kankerbestrijding
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Oncology › PARP inhibition in cancer therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- DNA damage response, chemoresistance, synthetic lethality, homologous recombination deficiency, DNA repair deficiency, acquired drug resistance
- MeSH terms
- Antineoplastic Agents, DNA Damage, DNA Repair, Neoplasms, Signal Transduction, Genes, p53, Drug Resistance, Neoplasm
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