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Nucleotide metabolism, oncogene-induced senescence and cancer
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Senescence is defined as a stable cell growth arrest. Oncogene-induced senescence (OIS) occurs when an activated oncogene is expressed in a normal cell. OIS acts as a bona fide tumor suppressor mechanism by driving stable growth arrest of cancer progenitor cells harboring the initial oncogenic hit. OIS is often characterized by aberrant DNA replication and the associated DNA damage response. Nucleotides, in particular deoxyribonucleotide triphosphates (dNTPs), are necessary for both DNA replication and repair. Imbalanced dNTP pools play a role in a number of human diseases, including during the early stages of cancer development. This review will highlight what is currently known about the role of decreased nucleotide metabolism in OIS, how nucleotide metabolism leads to transformation and tumor progression, and how this pathway can be targeted as a cancer therapeutic by inducing senescence of cancer cells.
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“Moreover, during OIS, fatty acid metabolism is altered, glucose consumption is enhanced, and the utilization of pyruvate in the tricarboxylic acid cycle and nucleotide deficiency are increased [119,216,217,218,219].”
From Mechanisms and Regulation of Cellular Senescence (2021) · cites this paper as [219]
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Metadata
- Authors
- Aird, K. M., & Zhang, R.
- Affiliations
- The Wistar Institute (US)
- Corresponding author
- Zhang, Rugang
- Venue
- Cancer Letters
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 356
- Issue
- 2
- Pages
- 204-210
- ISSN
- 0304-3835 (ISSN-L)
- PMC
- PMC4115046
- OpenAlex
- W1974913955
- Cited by
- 166
- References
- 109
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 31 · 2023: 17 · 2022: 22 · 2021: 17 · 2020: 11 · 2019: 10 · 2018: 11 · 2017: 6 · 2016: 12 · 2015: 6
- FWCI
- 1.10
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cancer Letters (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (CA010815, T32CA9171-35, R01CA160331, R01CA163377, T32CA009171, P30CA010815)
- Ovarian Cancer Academy
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- oncogene-induced senescence, nucleotide metabolism, dNTP pools, DNA replication, DNA damage response, tumor suppression, tumor progression, cellular senescence, cancer therapy, DNA repair
- MeSH terms
- Cell Transformation, Neoplastic, Deoxyribonucleotides, DNA Damage, DNA Repair, DNA Replication, Humans, Neoplasms, Oncogenes, Biomarkers, Tumor, Neoplastic Stem Cells, Signal Transduction, Cellular Senescence, Cell Proliferation
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