The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
p53 modulation of the DNA damage response
Abstract
The tumor suppressor p53 plays a central role in the DNA damage response. After exposure to genotoxic stress, p53 can both positively and negatively regulate cell fate. Initially, p53 promotes cell survival by inducing cell cycle arrest, DNA repair, and other pro‐survival pathways. However, when cells accumulate DNA damage or demonstrate aberrant growth, p53 can direct the elimination of damaged cells. In this review, we will discuss the transcriptional‐dependent and ‐independent roles of p53 in regulating the DNA damage response. J. Cell. Biochem. 100: 883–896, 2007. © 2006 Wiley‐Liss, Inc.
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A DNA damage checkpoint response in telomere-initiated senescence
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“Interestingly, Serine-15 phosphorylated p53 and p21 accumulate during replicative senescence suggesting that telomere shortening may trigger a DNA damage signal similar to that seen with DNA double-strand breaks (DSBs) [d’Adda di Fagagna et al., 2003].”
BackgroundPromotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene
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p53 ubiquitination: Mdm2 and beyond
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A ribonucleotide reductase gene involved in a p53-dependent cell-cycle checkpoint for DNA damage
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PPM1D dephosphorylates Chk1 and p53 and abrogates cell cycle checkpoints
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p53 and DNA damage-inducible expression of the xeroderma pigmentosum group C gene
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p21 Inhibits Thr161 Phosphorylation of Cdc2 to Enforce the G2 DNA Damage Checkpoint
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Cyclin G Recruits PP2A to Dephosphorylate Mdm2
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Self-citationIncreased Susceptibility to UV-Induced Skin Carcinogenesis in Polymerase η–deficient Mice
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Cited by
Radiation-induced cell death mechanisms
Eriksson, D., & Stigbrand, T. (2010) · Tumor Biology · doi:10.1007/s13277-010-0042-8 · Cited by 666
The expanding universe of p53 targets
Menendez, D., Inga, A., & Resnick, M. A. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2730 · Cited by 568
Acetylation Is Crucial for p53-Mediated Ferroptosis and Tumor Suppression
Wang, S.-J., Li, D., Ou, Y., Jiang, L., Chen, Y., Zhao, Y., & Gu, W. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.022 · Cited by 462
Proliferative capacity of corneal endothelial cells
Joyce, N. C. (2012) · Experimental Eye Research · doi:10.1016/j.exer.2011.08.014 · Cited by 347
Yokoyama, Y., Sasaki, Y., Terasaki, N., Kawataki, T., Takekawa, K., Iwase, Y., Shimizu, T., Sanoh, S., & Ohta, S. (2018) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00913 · Cited by 160
Metadata
- Authors
- Helton, E. S., & Chen, X.
- Venue
- Journal of Cellular Biochemistry
- Publisher
- Wiley
- Published
- 2006-10-09
- Volume
- 100
- Issue
- 4
- Pages
- 883-896
- ISSN
- 0730-2312 (ISSN-L)
- 1097-4644
- OpenAlex
- W1973788312
- Cited by
- 293
- References
- 17
- FWCI
- 9.92
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
