The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Co-localization of mutant p53 and amyloid-like protein aggregates in breast tumors
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Amyloid aggregates caused by TP53 mutations have been found in biopsy specimens from ovarian and breast cancers.484,485”
From Targeting p53 pathways: mechanisms, structures, and advances in therapy (2023) · cites this paper as [484]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Vogelstein, B., Lane, D., & Levine, A. J. (2000) · Nature · doi:10.1038/35042675 · Cited by 6,607
TP53 mutations in human cancers: origins, consequences, and clinical use.
Olivier, M., Hollstein, M., & Hainaut, P. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001008 · Cited by 2,199 · cited 3×
“Around 90% of the mutations are located at the central DNA-binding domain (Petitjean et al., 2007; Olivier et al., 2010).”
BackgroundTP53 mutations in human cancers: Functional selection and impact on cancer prognosis and outcomes
Petitjean, A., Achatz, M. I. W., Borresen-Dale, A. L., Hainaut, P., & Olivier, M. (2007) · Oncogene · doi:10.1038/sj.onc.1210302 · Cited by 884
p53 isoforms can regulate p53 transcriptional activity
Bourdon, J.-C., Fernandes, K., Murray-Zmijewski, F., Liu, G., Diot, A., Xirodimas, D. P., Saville, M. K., & Lane, D. P. (2005) · Genes & Development · doi:10.1101/gad.1339905 · Cited by 810
Structural Classification of Toxic Amyloid Oligomers
Glabe, C. G. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800016200 · Cited by 783
The complexity of p53 stabilization and activation
Lavin, M. F., & Gueven, N. (2006) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4401925 · Cited by 701
Research works printed but not linked: 17
- Ano Bom, 2009, The p53 core domain is a molten globule at low pH: functional implications of an intrinsically partially unfolded structure, J Biol Chem, 285, 2857, 10.1074/jbc.M109.075861 · DOI
- Courtois, 2004, P53 protein variants: structural and functional similarities with p63 and p73 isoforms, Oncogene, 23, 631, 10.1038/sj.onc.1206929 · DOI
- Elston, 1991, Pathological prognostic factors in breast cancer. I. The value of histological grade in breast cancer: experience from a large study with long-term follow-up, Histopathology, 19, 403, 10.1111/j.1365-2559.1991.tb00229.x · DOI · Paper page
- Glabe, 2004, Conformation-dependent antibodies target diseases of protein misfolding, Trends Biochem Sci, 29, 542, 10.1016/j.tibs.2004.08.009 · DOI
- Higashimoto, 2006, Unfolding, aggregation, and amyloid formation by the tetramerization domain from mutant p53 associated with lung cancer, Biochemistry, 45, 1608, 10.1021/bi051192j · DOI · Paper page
- Ishimaru, 2003, Fibrillar aggregates of the tumor suppressor p53 core domain, Biochemistry, 42, 9022, 10.1021/bi034218k · DOI · Paper page
- Ishimaru, 2004, Reversible aggregation plays a crucial role on the folding landscape of p53 core domain, Biophys J, 87, 2691, 10.1529/biophysj.104.044685 · DOI
- Ishimaru, 2009, Cognate DNA stabilizes the tumor suppressor p53 and prevents misfolding and aggregation, Biochemistry, 48, 6126, 10.1021/bi9003028 · DOI
- Langer⊘d, 2007, TP53 mutation status and gene expression profiles are powerful prognostic markers of breast, Breast Cancer Res, 9, R30, 10.1186/bcr1675 · DOI · Paper page
- Lee, 2003, Reversible amyloid formation by the p53 tetramerization domain and a cancer-associated mutant, J Mol Biol, 327, 699, 10.1016/S0022-2836(03)00175-X · DOI
- Oren, 2010, Mutant p53 gain-of-function in cancer, Cold Spring Harb Perspect Biol, 2, a001107, 10.1101/cshperspect.a001107 · DOI · Paper page
- Olivier, 2006, The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer, Clin Cancer Res, 12, 1157, 10.1158/1078-0432.CCR-05-1029 · DOI · Paper page
- Rigacci, 2008, The (1–63) region of the p53 transactivation domain aggregates in vitro into cytotoxic amyloid assemblies, Biophys J, 94, 3635, 10.1529/biophysj.107.122283 · DOI
- Sanchez-Ruiz, 2010, Protein kinetic stability, Biophys Chem, 148, 1, 10.1016/j.bpc.2010.02.004 · DOI · Paper page
- Silva, 2010, Ligand binding and hydration in protein misfolding: insights from studies of prion and p53 tumor suppressor protein, Acc Chem Res, 43, 271, 10.1021/ar900179t · DOI
- Simao, 2002, TP53 mutations in breast cancer tumors of patients from Rio de Janeiro Brazil: association with risk factors and tumor characteristics, Int J Cancer, 101, 69, 10.1002/ijc.10567 · DOI
- Uversky, 2010, Mysterious oligomerization of the amyloidogenic proteins, FEBS J, 2940, 10.1111/j.1742-4658.2010.07721.x · DOI · Paper page
Cited by
Targeting p53 pathways: mechanisms, structures, and advances in therapy
Wang, H., Guo, M., Wei, H., & Chen, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01347-1 · Cited by 1,016
Targeting mutant p53 for efficient cancer therapy
Bykov, V. J. N., Eriksson, S. E., Bianchi, J., & Wiman, K. G. (2018) · Nature Reviews Cancer · doi:10.1038/nrc.2017.109 · Cited by 889
A Designed Inhibitor of p53 Aggregation Rescues p53 Tumor Suppression in Ovarian Carcinomas
Soragni, A., Janzen, D. M., Johnson, L. M., Lindgren, A. G., Thai-Quynh Nguyen, A., Tiourin, E., Soriaga, A. B., Lu, J., Jiang, L., Faull, K. F., et al. (2016) · Cancer Cell · doi:10.1016/j.ccell.2015.12.002 · Cited by 341
(2019) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2019.08.002 · Cited by 78
Self-citation
Metadata
- Authors
- Levy, C. B., Stumbo, A. C., Ano Bom, A. P. D., Portari, E. A., Carneiro, Y., Silva, J. L., & De Moura-Gallo, C. V.
- Venue
- The International Journal of Biochemistry & Cell Biology
- Publisher
- Elsevier BV
- Published
- 2011-01
- Volume
- 43
- Issue
- 1
- Pages
- 60-64
- ISSN
- 1357-2725
- Cited by
- 144
- References
- 6
- Language
- en
- Update notices
- erratum (2011-06-01)
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
About these checks
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 ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Co-localization of mutant p53 and amyloid-like protein aggregates in breast tumors. https://app.cochat.ai/papers/10.1016/j.biocel.2010.10.017
- The paper
- Levy, C. B., Stumbo, A. C., Ano Bom, A. P. D., Portari, E. A., Carneiro, Y., Silva, J. L., & De Moura-Gallo, C. V. (2011). Co-localization of mutant p53 and amyloid-like protein aggregates in breast tumors. The International Journal of Biochemistry & Cell Biology. https://doi.org/10.1016/j.biocel.2010.10.017
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.