New Roles of Cyclin D1
Open accessAbstract
Cyclins encode regulatory subunits of holoenzymes that phosphorylate a variety of cellular substrates. Although the classic role of cyclins in cell cycle progression and tumorigenesis has been well characterized, new functions have been identified, including the induction of cellular migration and invasion, enhancement of angiogenesis, inhibition of mitochondrial metabolism, regulation of transcription factor signaling via a DNA-bound form, the induction of chromosomal instability, enhancement of DNA damage sensing and DNA damage repair, and feedback governing expression of the noncoding genome. This review describes the mechanisms of these new functions of cyclin D1.
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Cyclin D1 and the CDK4-related kinase CDK6 can associate with target genes and function as transcriptional regulators.
“Previous studies revealed that Cyclin D140,41 as well as the CDK4-related kinase CDK642 can associate with target genes and function as transcriptional regulators.”
From CDK4 inhibition diminishes p53 activation by MDM2 antagonists (2018) · cites this paper as [40]
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- Authors
- Pestell, R. G.
- Affiliations
- Thomas Jefferson University (US)
- Corresponding author
- Pestell, Richard G.
- ORCID
- Pestell, Richard G.
- Venue
- The American Journal of Pathology
- Publisher
- Elsevier BV
- Published
- 2013-07
- Volume
- 183
- Issue
- 1
- Pages
- 3-9
- ISSN
- 0002-9440 (ISSN-L)
- PMC
- PMC3702737
- OpenAlex
- W1988043615
- Cited by
- 197
- References
- 60
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 8 · 2023: 9 · 2022: 9 · 2021: 20 · 2020: 19 · 2019: 16 · 2018: 21 · 2017: 23 · 2016: 25 · 2015: 26 · 2014: 15 · 2013: 2
- FWCI
- 2.40
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- American Journal Of Pathology (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Breast Cancer Research Foundation
- Pennsylvania Department of Health
- Dr. Ralph and Marian Falk Medical Research Trust
- National Institutes of Health (R01CA70896)
- National Cancer Institute (R01CA137494, R01CA086072, R01CA075503, R01CA070896, R01CA132115, P30CA056036)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- cyclin D1, cyclins, cell cycle regulation, carcinogenesis, cell migration, tumor invasion, angiogenesis, mitochondrial metabolism, transcription factor signaling, chromosomal instability, DNA damage recognition, DNA repair, non-coding genome
- MeSH terms
- Animals, Cell Cycle, DNA Repair, Gene Expression Regulation, Humans, Mitochondria, Cyclin D1, Chromosomal Instability, Mice
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