The DOI matches its Crossref record; 159 of the 159 references it cites were found in a registry or an index.
Targeting mutant p53 for efficient cancer therapy
Abstract
The tumour suppressor gene TP53 is the most frequently mutated gene in cancer. Wild-type p53 can suppress tumour development by multiple pathways. However, mutation of TP53 and the resultant inactivation of p53 allow evasion of tumour cell death and rapid tumour progression. The high frequency of TP53 mutation in tumours has prompted efforts to restore normal function of mutant p53 and thereby trigger tumour cell death and tumour elimination. Small molecules that can reactivate missense-mutant p53 protein have been identified by different strategies, and two compounds are being tested in clinical trials. Novel approaches for targeting TP53 nonsense mutations are also underway. This Review discusses recent progress in pharmacological reactivation of mutant p53 and highlights problems and promises with these strategies.
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“Consequently, a potential avenue for addressing chemotherapy resistance involves reactivating mutant p53 (64).”
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BackgroundInfluentialAssociations of MDM2 and MDM4 Polymorphisms with Early-Stage Breast Cancer
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“Moreover, it is established that TP53 pathway is one of the central pathways involved in various human cancers, including breast cancer [23,44,45].”
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“Transcription factor p53 acts as a cellular stress sensor in response to DNA damage and oncogenic stress (94) and often mutates in different types of human cancers (109).”
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BackgroundInfluentialQSER1 preserves the suppressive status of the pro-apoptotic genes to prevent apoptosis
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“This suggests that strategies of a high overexpression of wt p53 as well as a mutant p53 conversion into wt-like conformation and activity [5, 81] are worthy efforts in finding methods to treat cancers with the accumulated mutant p53.”
Small Molecules Targeting Mutant P53: A Promising Approach for Cancer Treatment
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“Despite the ongoing efforts, small molecules re-activating mutant p53 are still in clinical development [11].”
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“TP53 can trigger cell death by apoptosis through transactivation of downstream target genes [37,38], but mutations in TP53 would promote malignant progression and lead to insensitivity of tumor cells toward chemotherapy [39].”
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Buxus alkaloid compound destabilizes mutant p53 through inhibition of the HSF1 chaperone axis
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“As a key anti-cancer protein with growth inhibitory function, p53 can regulate the cell cycle and promote cell apoptosis or senescence, thus inhibiting tumorigenesis (43).”
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“In addition to chemotherapy and surgery, radiotherapy, immunotherapy, and gene therapy may also be used as treatment strategies (Bykov et al. 2018).”
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Metadata
- Authors
- Bykov, V. J. N., Eriksson, S. E., Bianchi, J., & Wiman, K. G.
- Affiliations
- Karolinska Institutet (SE)
- Corresponding author
- Wiman, Klas G.
- Venue
- Nature Reviews Cancer
- Published
- 2017-12-15
- Volume
- 18
- Issue
- 2
- Pages
- 89-102
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2772062014
- Cited by
- 889
- References
- 159
- Citations by year
- 2026: 43 · 2025: 70 · 2024: 100 · 2023: 132 · 2022: 126 · 2021: 150 · 2020: 129 · 2019: 88 · 2018: 49 · 2017: 1
- FWCI
- 7.67
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- TP53, mutant p53, p53 reactivation, missense mutations, nonsense mutation, tumor suppressor, cancer therapy, cancer cell death, clinical trials
- MeSH terms
- Animals, Antineoplastic Agents, Humans, Mutation, Neoplasms, Tumor Suppressor Protein p53, Cell Death, Mutant Proteins
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