The DOI matches its Crossref record; 93 of the 93 references it cites were found in a registry or an index.
Apoptosis - the p53 network
Abstract
Exposure to cellular stress can trigger the p53 tumor suppressor, a sequence-specific transcription factor, to induce cell growth arrest or apoptosis. The choice between these cellular responses is influenced by many factors, including the type of cell and stress, and the action of p53 co-activators. p53 stimulates a wide network of signals that act through two major apoptotic pathways. The extrinsic, death receptor pathway triggers the activation of a caspase cascade, and the intrinsic, mitochondrial pathway shifts the balance in the Bcl-2 family towards the pro-apoptotic members, promoting the formation of the apoptosome, and consequently caspase-mediated apoptosis. The impact of these two apoptotic pathways may be enhanced when they converge through Bid, which is a p53 target. The majority of these apoptotic effects are mediated through the induction of specific apoptotic target genes. However, p53 can also promote apoptosis by a transcription-independent mechanism under certain conditions. Thus, a multitude of mechanisms are employed by p53 to ensure efficient induction of apoptosis in a stage-, tissue- and stress-signal-specific manner. Manipulation of the apoptotic functions of p53 constitutes an attractive target for cancer therapy.
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“Apoptosis, both intrinsic and extrinsic, is induced via p53 target genes.176, 177”
From Census and evaluation of p53 target genes (2017) · cites this paper as [176]
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Metadata
- Authors
- Haupt, S., Berger, M., Goldberg, Z., & Haupt, Y.
- Affiliations
- Hebrew University of Jerusalem (IL)
- Corresponding author
- Haupt, Ygal
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2003-10-15
- Volume
- 116
- Issue
- 20
- Pages
- 4077-4085
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W2103616303
- Cited by
- 1,136
- References
- 93
- Citations by year
- 2026: 11 · 2025: 24 · 2024: 34 · 2023: 31 · 2022: 37 · 2021: 53 · 2020: 57 · 2019: 57 · 2018: 57 · 2017: 53 · 2016: 75 · 2015: 66 · 2014: 59 · 2013: 76 · 2012: 76
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Keywords
- p53, apoptosis, p53 tumor suppressor, cellular stress response, growth arrest, death receptor signaling, mitochondrial apoptosis, Bcl-2 family proteins, apoptosome, caspase cascade, Bid, p53 target genes, cancer therapy
- MeSH terms
- Animals, Carrier Proteins, Cell Division, Enzyme Activation, Humans, Mitochondria, Proto-Oncogene Proteins, Signal Transduction, Tumor Suppressor Protein p53, Apoptosis, Protein Serine-Threonine Kinases, Proto-Oncogene Proteins c-bcl-2, Caspases, Protein Interaction Mapping, BH3 Interacting Domain Death Agonist Protein, Proto-Oncogene Proteins c-akt
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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