Cell cycle arrest is not senescence
Open accessAbstract
DNA damaging agents and radiation, cytotoxins and anti-cancer drugs, telomere erosion and cytokines, culture shock and mitogenic stimuli, oncogenes and tumor suppressors can induce both cell cycle arrest and cellular senescence. Due to this semi-coincidence, senescence is confused with cell cycle arrest, or even more misleadingly, with growth inhibition. With such misconceptions, cellular senescence cannot be linked to organismal aging. Also, the relation between cancer and senescence is distorted. Here I discuss why the link between arrest and senescence is semi-coincidental and how senescence is related to aging and cancer.
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- Authors
- Blagosklonny, M. V.
- Affiliations
- Roswell Park Comprehensive Cancer Center (US)
- Corresponding author
- Blagosklonny, Mikhail V.
- Venue
- Aging
- Publisher
- Impact Journals, LLC
- Published
- 2011-02-06
- Volume
- 3
- Issue
- 2
- Pages
- 94-101
- ISSN
- 1945-4589 (ISSN-L)
- PMC
- PMC3082019
- OpenAlex
- W2161980885
- Cited by
- 217
- References
- 69
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 7 · 2023: 12 · 2022: 10 · 2021: 20 · 2020: 15 · 2019: 15 · 2018: 13 · 2017: 10 · 2016: 18 · 2015: 12 · 2014: 15 · 2013: 19 · 2012: 23
- FWCI
- 2.57
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Aging (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- cellular senescence, cell cycle arrest, biological aging, cancer, growth inhibition, telomere shortening, oncogenes, tumor suppressor, DNA damage, culture shock, cytokines
- MeSH terms
- Cell Cycle, Humans, Neoplasms, Cellular Senescence, Tumor Suppressor Proteins, TOR Serine-Threonine Kinases
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