Coping with stress: multiple ways to activate p53

Surfing the p53 network

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CDK inhibitors: positive and negative regulators of G1-phase progression

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The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

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In Vivo Activation of the p53 Pathway by Small-Molecule Antagonists of MDM2

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Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours

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Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms

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DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis

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PUMA, a Novel Proapoptotic Gene, Is Induced by p53

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The Role of Intrinsic Signaling Pathways in Cell Proliferation

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Topical delivery of DNA oligonucleotide to induce p53 generation in the skin via thymidine dinucleotide (pTT)-encapsulated liposomal carrier

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Hydrocarbon‐Stapled Helices: A Novel Approach for Blocking Protein‐Protein Interactions

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Cancer Gene Pathways

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Estimation of delays in generalized asynchronous Boolean networks

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Wuho/WDR4 deficiency inhibits cell proliferation and induces apoptosis via DNA damage in mouse embryonic fibroblasts

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Chemical Carcinogenesis

Hofseth, L. J., Weston, A., & Harris, C. C. (2022) · Wiley eBooks · doi:10.1002/9781119000822.hfcm023.pub2 · Cited by 4

Transcriptional mutagenesis dramatically alters genome-wide p53 transactivation landscape

Liang, S., Ezerskyte, M., Wang, J., Pelechano, V., & Dreij, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-70412-4 · Cited by 3

Distinct p53 phosphorylation patterns in chronic lymphocytic leukemia patients are reflected in the activation of circumjacent pathways upon DNA damage

Mančíková, V., Pešová, M., Pavlová, Š., Helma, R., Závacká, K., Hejret, V., Tauš, P., Hynšt, J., Plevová, K., Malčíková, J., et al. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13337 · Cited by 3

The Anticancer Potentials of Substituted Indeno[1,2-b]quinoline Amines against HT29 and SW620: Experimental and In silico Approach

Ökten, S., Aydın, A. O., Erkan, S., & Tutar, A. (2023) · Letters in Drug Design & Discovery · doi:10.2174/1570180820666230201144615 · Cited by 3

Deciphering Internal Regulatory Patterns within the p53 Core Tetramer: Insights from Community Network Analysis

Zhou, H., & Yan, S. (2024) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.4c02382 · Cited by 3

DNA Damage Signaling Downstream of ATM

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Self-association of adenovirus type 5 E1B-55 kDa as well as p53 is essential for their mutual interaction

Morawska, M., Bieńkowska-Szewczyk, K., & Dobbelstein, M. (2009) · Oncogene · doi:10.1038/onc.2009.461 · Cited by 3

Wortmannin efficiently suppresses the recovery from radiation-induced damage in pimonidazole-unlabeled quiescent tumor cell population

Masunaga, S., Sakurai, Y., Tanaka, H., Suzuki, M., Kondo, N., Narabayashi, M., Maruhashi, A., & Ono, K. (2012) · Journal of Radiation Research · doi:10.1093/jrr/rrs094 · Cited by 3

Molecular Genetic Aspects of Malignant Colon Tumors

Пасевич, Д. М., Sushkou, S. A., & Семенов, В. М. (2016) · Novosti hirurgii · doi:10.18484/2305-0047.2016.2.184 · Cited by 3

ZNF509S1 downregulates PUMA by inhibiting p53K382 acetylation and p53-DNA binding

Jeon, B.-N., Yoon, J.-H., Han, D., Kim, M.-K., Kim, Y., Choi, S.-H., Song, J.-Y., Kim, K., Kim, K., & Hur, M. (2017) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2017.07.008 · Cited by 5

Exploring the Influence of Parameters on the p53 Response When Single-Stranded Breaks and Double-Stranded Breaks Coexist

Ma, A., & Dai, X. (2019) · Interdisciplinary Sciences Computational Life Sciences · doi:10.1007/s12539-019-00332-z · Cited by 3

Complex p53 dynamics regulated by miR-125b in cellular responses to reactive oxidative stress and DNA damage

Malik, M. Z., DASHTI, M. H., Jangid, A., Channanath, A. M., John, S. E., Singh, R. K. B., Al‐Mulla, F., & Thanaraj, T. A. (2024) · Briefings in Bioinformatics · doi:10.1093/bib/bbae706 · Cited by 2

Minichromosome maintenance 4 plays a key role in protecting against acute kidney injury by regulating tubular epithelial cells survival and regeneration

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The Effect of p53 Status of Tumor Cells on Radiosensitivity of Irradiated Tumors With Carbon-Ion Beams Compared With γ-Rays or Reactor Neutron Beams

Masunaga, S., Uzawa, A., Hirayama, R., Matsumoto, Y., Sakurai, Y., Tanaka, H., Tano, K., Sanada, Y., Suzuki, M., Maruhashi, A., et al. (2015) · World Journal of Oncology · doi:10.14740/wjon941w · Cited by 2

[Advances in the study of p53 in response to DNA damage].

Wang, Y., Sun, H., Liu, G.-T., & Chen, X. (2011) · PubMed · Cited by 2

p53 REEPs to sow ER–mitochondrial contacts

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Polymorphysm of tumor supressor gene tp53 among healthy donors and patients with rectal cancer

Волков, А. Н., Padukova, A. D., P.V., P. V., & Кутихин, А. Г. (2019) · Экспериментальная и клиническая гастроэнтерология · doi:10.31146/1682-8658-ecg-162-2-45-49 · Cited by 2

The p53-Mdm2 Loop: A Critical Juncture of Stress Response

Levav-Cohen, Y., Goldberg, Z., Alsheich-Bartok, O., Zuckerman, V., Haupt, S., & Haupt, Y. (2010) · Molecular biology intelligence unit · doi:10.1007/978-1-4419-8231-5_5 · Cited by 2

Cancer Gene Pathways

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P53, ROS: Redox Regulation Signaling, Metabolic Reprogramming, and Autophagy in Cancer

Bansal, M. P. (2023) · Springer eBooks · doi:10.1007/978-981-99-7342-2_7 · Cited by 2

Dependency of repair of radiation-induced damage on p53 status and efficient inhibition of the repair with wortmannin treatment in vivo, with reference to the effect on intratumor quiescent cell population

Masunaga, S., Takahashi, A., Ohnishi, K., Nagata, K., Suzuki, M., Kashino, G., Kinashi, Y., Ohnishi, T., & Ono, K. (2007) · Oncology Reports · doi:10.3892/or.18.6.1589 · Cited by 2

Effects of p53 Status of Tumor Cells and Combined Treatment With Mild Hyperthermia, Wortmannin or Caffeine on Recovery From Radiation-Induced Damage

Masunaga, S., Tano, K., Sanada, Y., Suzuki, M., Takahashi, A., Ohnishi, K., & Ono, K. (2019) · World Journal of Oncology · doi:10.14740/wjon1203 · Cited by 2

Transcriptomic response of prostate cancer cells to carbon ion and photon irradiation with focus on androgen receptor and TP53 signaling

Hänze, J., Mengen, L. M., Mernberger, M., Tiwari, D. K., Plagge, T., Nist, A., Subtil, F. S. B., Theiß, U., Eberle, F., Roth, K. S., et al. (2024) · Radiation Oncology · doi:10.1186/s13014-024-02480-z · Cited by 1

ENY2 transcription and export complex 2 subunit deficiency induces nucleolar stress to inhibit tumor progression through NPM1/MDM2/p53-dependent and -independent responses

Zuo, S., He, S., Zhu, Z., Hou, Y., Wu, Z., Tang, Y., & Zou, Y. (2026) · Cellular Oncology · doi:10.1007/s13402-025-01148-4 · Cited by 2

BAY 61-3606, CDKi, and Sodium Butyrate Treatments Modulate p53 Protein Level and Its Site-Specific Phosphorylation in Human Vestibular Schwannomas In Vitro

Mitra, R., Keshava, R., Jothi, M., Vazhayil, V. V., Bhagavatula, I. D., & Gope, R. (2014) · Journal of Cancer Research · doi:10.1155/2014/249354 · Cited by 1

Pathogenesis of Merkel Cell Carcinoma

Becker, J. C., & Houben, R. (2010) · Springer eBooks · doi:10.1007/978-3-642-05072-5_14 · Cited by 1

Targeting Myc-driven tumours - BETing on ATR

Muralidharan, S. V. (2016) · Cited by 1

New Perspectives in Cancer Therapy: The Biotin-Antitumor Molecule

Mandracchia, D., Collina, S., Rui, M., & Rossi, D. (2014) · Cited by 1

Silencing of Mutant p53 Leads to Suppression of Human Breast Xenograft Tumor Growth in vivo

Park, W., Park, S.-R., Park, H.-J., Bae, Y.-H., Ryu, H. S., Jang, H., Bae, M., & Bae, S. (2016) · KSBB Journal · doi:10.7841/ksbbj.2016.31.1.52 · Cited by 1

Branching into metabolism

Ide, T., Chu, K., Aaronson, S. A., & Lee, S. W. (2010) · Cited by 1

p53 Binding Loci Database (p53BLD): a repository for the genome-wide binding loci of human TP53

Wu, W.-S., Chang, J.-W., Liaw, H., Chu, Y.-H., & Jiang, Y.-X. (2019) · Clinical Microbiology and Research · doi:10.31487/j.cmr.2018.01.01 · Cited by 1

ROS

Zhang, W., & Huang, P. (2017) · Springer eBooks · doi:10.1007/978-1-4419-0717-2_20 · Cited by 1

Cancer Gene Pathways

Bunz, F. (2022) · Springer eBooks · doi:10.1007/978-3-030-99387-0_6 · Cited by 1

Investigation of robustness and dynamic behaviour of G1/S checkpoint/DNA-damage signal transduction pathway based on mathematical modelling and a novel neural network approach

Ling, H. (2011) · Lincoln University Research Archive (Lincoln University) · Cited by 2

Post-translational Modifications of the p53 Protein and the Impact in Alzheimer’s Disease: A Review of the LiteraturePreprint

Clark, J., Piccirella, S., Kayed, R., Abate, G., Uberti, D. L., & Kinnon, P. (2021) · Preprints.org · doi:10.20944/preprints202109.0359.v1 · Cited by 1

Building p53: Figure 1.Preprint

Terzian, T., & Lozano, G. (2010) · Genes & Development · doi:10.1101/gad.1988510 · Cited by 3

Subgroups of Merkel cell carcinoma patients defined by young age, immunodeficiency and polyomavirus infection

Sahi, H. (2014) · Työväentutkimus Vuosikirja

The regulation of RNA polymerase III-mediated transcription by p53, AP-1 and JNKs

Dowding, S. N. (2013) · Enlighten: Theses (The University of Glasgow)

DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation

McNamee, L. M. (2008) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/y5k8-fb94

Identification and characterization of a proteasome deubiquitinase inhibitor

Brnjic, S. (2014) · Figshare

Función del gen Snai3 (Smuc) en la transición epitelio mesenquimal y en cáncer

Gutsche, K. (2009) · Gredos (University of Salamanca) · doi:10.14201/gredos.76287

Analysis of p53 and c-MYC, two key transcription factors involved in tumorigenesis

Jung, P. (2008) · doi:10.5282/edoc.10559

Efeitos do Silenciamento de E2F1 e HEB, Fatores de Transcrição Preditos In Silico, em Células de Glioblastoma Irradiadas com Raios Gama.

Godoy, P. R. D. V. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2013.tde-13062013-094602

Uncovering the Basis of ATP Hydrolysis Activity in Purified Human p53 Protein: A Reinvestigation

Verma, S., & Rao, B. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093652

Oncogene-Induced Senescence (OIS) as a Cellular Response to Oncogenic Stresses

Bourdeau, V., & Ferbeyre, G. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1075-2_3

Use of diagnostic and therapeutic biomarkers in personalized oncology based on adult T-cell leukemia/lymphoma research

Hasegawa, H., & Kamihira, S. (2013) · Personalized Medicine Universe · doi:10.1016/j.pmu.2013.05.001

Construction and characterization of a cDNA library from human brain glioma cell line U251 with overexpressed exogenous p53 gene

Shu, K., Li, Y.-Z., Shao, H., Zhang, M., & Wu, L. (2010) · Knowledge Repository of Yantai Institute of Coastal Zone Research, CAS (Yantai Institute of Coastal Zone Research) · doi:10.5897/ajb09.1754

Identification and validation of therapeutic targets in sarcoma models

Maruwge, W. (2009) · Figshare

Mdm2 phosphorylations : Characterization and applications

Malmlöf, M. (2007) · Figshare

CARF Regulates Cellular Senescence and Apoptosis through p53-Dependent and -Independent Pathways

Wadhwa, R., Singh, R., Kaul, Z., & Kaul, S. C. (2013) · Humana Press eBooks · doi:10.1007/978-1-62703-456-2_8

ИЗУЧЕНИЕ ОСОБЕННОСТЕЙ ЭКСПРЕСИИ ГЕНОВ ДНК-РЕПАРИРУЮЩИХ МЕХАНИЗМОВ В РАКОВЫХ КЛЕТКАХ С НОРМАЛЬНЫМ И МУТАНТНЫМ ГЕНОМ ТР53

Шутов, А. М. (2013)

Bedeutung der c-Abl-Aktivität für die Reaktion auf DNA-Schädigung und für die genetische Stabilität Bcr-Abl-negativer Zellen Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften (Dr. rer. nat.)

Naturwissenschaften, F., & Fischer-Bosch-Institut, M. (2011)

Molecular Mechanisms Underlying the Oncogenic Function of SS18 and SSX

D’Arcy, P. (2008) · Figshare

THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS

Kong, B. (2015) · uO Research (University of Ottawa) · doi:10.20381/ruor-6589

Expressão gênica e proteica das isoformas A e B do receptor de progesterona, de p53 e de p21 em miométrio e leiomioma uterino

Lora, V. (2010) · Americanae (AECID Library)

Autophagy in Metabolism, Cell Death, and Leukemogenesis

Altman, B. J. (2011) · DukeSpace (Duke University)

Dynamical patterns of p53 states driven by PMLPreprint

Alam, M. J., Al-Shammari, E., & Singh, R. K. B. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1504.05084

Molecular Subtyping of Lung Carcinomas for Targeted Therapy

Oliveira, A. M. C. S. (2012) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/x50y-a570

Inference of asynchronous Boolean network from biological pathways

Das, H., & Layek, R. K. (2015) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2015.7319090

Molecular Insights into the Regulation of Apoptosis and Cellular Senescence and Their Implications for Cancer

Johmura, Y., & Nakanishi, M. (2016) · Springer eBooks · doi:10.1007/978-4-431-55873-6_18

Basic Pathobiology of Merkel Cell Carcinoma

Becker, J. C., Schrama, D., & Houben, R. (2010) · Modecular medicine and medicinal · doi:10.1142/9781848163140_0002

CIRCUMVENTING CISPLATIN RESISTANCE IN OVARIAN CANCERS THROUGH REACTIVATION OF p53 BY NON-CROSS-RESISTANT PLATINUM ANALOGS

Martinez-Rivera, M. (2016) · Digital Commons-TMC (Texas Medical Center)

Changing the balance in apoptosis: key to enhance cisplatin sensitivity of testicular cancer

Koster, R. (2010) · University of Groningen research database (University of Groningen / Centre for Information Technology)

Regulation of BTRC by gain-of-function TP53 mutation(s) in cancer cells

Xu, W. (2015) · TSpace (University of Toronto)

The p53 family interacting pathways in carcinogenesis and cellular response to DNA damage

Johnson, J. L. (2007) · doi:10.6083/m42f7kd0

Characterization and functional analysis of mutant p53 secretome in human cancer

Shakya, R. (2016) · Adelaide Research & Scholarship (AR&S) (University of Adelaide) · doi:10.4225/55/58d1bef2e0a57

Efeito da proteína p53 nas respostas celulares à terapia fotodinâmica com 1,9-dimetil azul de metileno

Abrantes, A. B. D. P. (2017) · doi:10.11606/d.46.2017.tde-21062017-104426

A novel role for p53 in self-tolerance

Larsen, B. M., & Bhandoola, A. (2017) · Blood · doi:10.1182/blood-2017-06-789115

Gain-of-function and dominant-negative effects of distinct p53 mutations in lung tumours

Turrell, F. K. (2018) · Apollo (University of Cambridge) · doi:10.17863/cam.18854

ASPP-MEDIATED DEPHOSPHORYLATION OF P53 BY PROTEIN PHOSPHATASE 1C

Millott, R. (2017) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3qf8jz7f

Effect of Maternal Age on Transcriptome of Granulosa Cells from Bovine Dominant Follicles

Khan, M. I. (2014) · University Library - University of Saskatchewan (University of Saskatchewan)

Nuclear Factor I in Malignant Glioma

Brun, M. M. (2015) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3t14v396

The role of PATZ1 transcription factor in the DNA damage response

Deniz, E. (2014) · Sabanci University

Secreção de Gaussia luciferase como indicador de atividade de caspase-3/7 em resposta ao tratamento com AdCDKN2AIRESp53 em glioblastoma multiforme.

Oliveira, D. V. C. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2019.tde-18022019-101454

Mechanisms of cytotoxicity induced by halobenzoquinone water disinfection byproducts

Li, J. (2017) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3q815824

Ubiquitous Merkel Cell Polyomavirus: Causative Agent of the Rare Merkel Cell Carcinoma

Shahzad, N., Gilani, U. S., Mahmood, M., Tasneem, F., Haque, M. F. U., & Hussain, I. (2021) · Springer eBooks · doi:10.1007/978-3-030-71165-8_17

Salvia Chinensia Benth Inhibits Triple Negative Breast Cancer Progression Through Inducing DNA Damage PathwayPreprint

Wang, K., Hu, Y., Xu, L., Zhao, S., Song, C., Sun, S., Zhao, Z., & Li, M. (2021) · Research Square · doi:10.21203/rs.3.rs-662543/v1

Presence of p53 Protein on Spermatozoa DNA: A Novel Environmental Bio-Marker and Implications for Male Fertility

Raimondo, S., Gentile, M., Gentile, T., & Montano, L. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.99559

Mecanismes de toxicitat de la dopamina en cèl·lules de neuroblastoma humà SH-SY5Y

Xavier, P. G. (2008) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)

Faculty Opinions recommendation of miR-380-5p represses p53 to control cellular survival and is associated with poor outcome in MYCN-amplified neuroblastoma.

Khosravi‐Far, R., & Datta, D. B. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5601962.6178055

Self-association of adenovirus 5 E1B-55 kDa as well as p53 is essential for their mutual interaction

Morawska, M. (2009) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3292

The tumour suppressor p53 as a supporter of DNA replication

Klusmann, I. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7143

MDM2 as a chromatin modifier

Gerber, S. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8184

Peer Review #1 of "The p53 signaling pathway of the large yellow croaker (Larimichthys crocea) responds to acute cold stress: evidence via spatiotemporal expression analysis of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt (v0.1)"

(2020) · PeerJ · doi:10.7287/peerj.10532v0.1/reviews/1

Mechanisms involved in quiescent blood vessel homeostasis

Fernández-Chacón, M. (2021) · Hispana

Faculty Opinions recommendation of Restoring synovial homeostasis in rheumatoid arthritis by targeting fibroblast-like synoviocytes.

Nakajima, T., & Fujita, H. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737940394.793577793

Melanoma

Lange, J. R., Fecher, L. A., Sharfman, W. H., Alani, R. M., Mikkilineni, R., Topalian, S. L., & Balch, C. M. (2008) · Elsevier eBooks · doi:10.1016/b978-0-443-06694-8.50077-4

Chemische Kanzerogenese

Fahrer, J., & Kaina, B. (2017) · doi:10.1002/9783527695447.ch7

Peer Review #3 of "The p53 signaling pathway of the large yellow croaker (Larimichthys crocea) responds to acute cold stress: evidence via spatiotemporal expression analysis of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt (v0.2)"

(2020) · PeerJ · doi:10.7287/peerj.10532v0.2/reviews/3

ROS

Zhang, W., & Huang, P. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6613-0_20-3

Peer Review #2 of "The p53 signaling pathway of the large yellow croaker (Larimichthys crocea) responds to acute cold stress: evidence via spatiotemporal expression analysis of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt (v0.1)"

(2020) · PeerJ · doi:10.7287/peerj.10532v0.1/reviews/2

Peer Review #3 of "The p53 signaling pathway of the large yellow croaker (Larimichthys crocea) responds to acute cold stress: evidence via spatiotemporal expression analysis of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt (v0.1)"

(2020) · PeerJ · doi:10.7287/peerj.10532v0.1/reviews/3

Unravelling mechanisms of p53-mediated tumour suppression

Bieging-Rolett, K. T., Mello, S. S., & Attardi, L. D. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3711 · Cited by 1,454

p53 at the Crossroads Between Stress Response Signaling and Tumorigenesis: From Molecular Mechanisms to Therapeutic Opportunities

Giono, L. E., Ladelfa, M. F., & Monte, M. (2014) · Springer eBooks · doi:10.1007/978-94-017-9421-3_4

Activation of the p53 tumor suppressor protein

Vousden, K. H. (2002) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/s0304-419x(02)00035-5 · Cited by 337

Activation and activities of the p53 tumour suppressor protein

Bálint, É., & Vousden, K. H. (2001) · British Journal of Cancer · doi:10.1054/bjoc.2001.2128 · Cited by 315

Regulation of the p53 response and its relationship to cancer

Meek, D. W. (2015) · Biochemical Journal · doi:10.1042/bj20150517 · Cited by 311