p53 and metabolism

On the origin of cancer cells

Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425

The Biology of Cancer: Metabolic Reprogramming Fuels Cell Growth and Proliferation

DeBerardinis, R. J., Lum, J. J., Hatzivassiliou, G., & Thompson, C. B. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.10.002 · Cited by 4,088

Development by Self-Digestion

Levine, B., & Klionsky, D. J. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00099-1 · Cited by 3,728

Blinded by the Light: The Growing Complexity of p53

Vousden, K. H., & Prives, C. (2009) · Cell · doi:10.1016/j.cell.2009.04.037 · Cited by 3,163

The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth

Christofk, H. R., Vander Heiden, M. G., Harris, M. H., Ramanathan, A., Gerszten, R. E., Wei, R., Fleming, M. D., Schreiber, S. L., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06734 · Cited by 2,820

Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis

DeBerardinis, R. J., Mancuso, A., Daikhin, E., Nissim, I., Yudkoff, M., Wehrli, S., & Thompson, C. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709747104 · Cited by 2,622

A model for p53-induced apoptosis

Polyak, K., Xia, Y., Zweier, J. L., Kinzler, K. W., & Vogelstein, B. (1997) · Nature · doi:10.1038/38525 · Cited by 2,500

Cancer cell metabolism: warburg and beyond

Hsu, P. P., & Sabatini, D. M. (2008) · Cell · doi:10.1016/j.cell.2008.08.021 · Cited by 2,452

p53 in health and disease

Vousden, K. H., & Lane, D. P. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2147 · Cited by 2,351

Metabolic adaptation and epigenetic modulations: Unraveling tumor plasticity under variable tumor microenvironment

Obeid, J. C. G., & Damaghi, M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13209-4.00012-x · Cited by 3

Genome-wide comparative analyses for selection signatures indicate candidate genes for between-breed variability in copper accretion in sheep

Adeniyi, O. O., Lenstra, J. A., Mastrangelo, S., & Lühken, G. (2024) · animal · doi:10.1016/j.animal.2024.101329 · Cited by 3

Biology – cancer metabolic phenotype

Čuperlović‐Culf, M. (2013) · Elsevier eBooks · doi:10.1533/9781908818263.15 · Cited by 3

THE CELLULAR PROCESS OF AUTOPHAGY AND CONTROL OF AUTOPHAGY IN NEURONS

McKnight, N. C., Mizushima, N., & Yue, Z. (2012) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814350457_0001 · Cited by 3

On the role of intrinsic noise on the response of the p53-Mdm2 module

Rodríguez, L. C., Figueroa-Morales, N., & Mulet, R. (2015) · Journal of Statistical Mechanics Theory and Experiment · doi:10.1088/1742-5468/2015/09/p09015 · Cited by 3

Structure–activity relationship study of 4-substituted piperidines at Leu26 moiety of novel p53–hDM2 inhibitors

Tian, Y., Ma, Y., Gibeau, C. R., Lahue, B. R., Shipps, G. W., Strickland, C., & Bogen, S. L. (2016) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2016.03.078 · Cited by 3

The Role of Energy Metabolism in Driving Disease Progression in Inflammatory, Hypoxic and Angiogenic Microenvironments

Phelan, J. J., Brown, C. O., Reynolds, J. V., & O'Sullivan, J. N. (2015) · Gastro - Open Journal · doi:10.17140/goj-1-108 · Cited by 3

Silibinin Protects Ultraviolet B–Irradiated Skin by Balancing Apoptosis and Autophagy in Epidermis and Dermis

Ikejima, T., & Hayashi, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00020-2 · Cited by 3

Apoptosis and autophagy markers predict survival in neoadjuvant treated oesophageal adenocarcinoma patients

El-Mashed, S., O’Donovan, T. R., Kay, E. W., O’Grady, A., McManus, D. T., Turkington, R. C., & McKenna, S. L. (2022) · BMC Cancer · doi:10.1186/s12885-022-09981-8 · Cited by 3

Pathophysiology of Cancer Cell Death

Galluzzi, L., Kepp, O., & Kroemer, G. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-2865-7.00005-9 · Cited by 4

WRAP53 Unwrapped; Roles in Nuclear Architecture and Cancer

Mahmoudi, S. (2011) · Figshare · Cited by 3

Novel insight into the mechanisms of neurotoxicity induced by glufosinate-ammonium via the microbiota-intestine-brain axis in Chinese mitten crab (Eriocheir sinensis)

Feng, H., Song, L., Wu, Y., Zhao, F., Zhu, F., Song, Z., Zhang, K., Jiang, J., Cai, X., Yin, S., et al. (2025) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2025.106426 · Cited by 2

Update and ADMET Profile of the Latin American Natural Product Database: LANaPDB

Gómez‐García, A., Lavecchia, M. J., Olmedo, D. A., Solís, P. N., & Medina‐Franco, J. L. (2025) · Molecular Informatics · doi:10.1002/minf.70013 · Cited by 2

Molecular mechanisms and recent advances in cellular senescence

Hussain, A., Tatar, M., & Gong, R. (2026) · Cell & Bioscience · doi:10.1186/s13578-026-01596-x · Cited by 2

KATP Channel Expression Determines ONC212 Sensitivity via Mitochondrial Dysfunction and PERK / ATF4 / CHOP Activation in Glioblastoma

Taskesen, A., & Hacıoğlu, C. (2026) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.71301 · Cited by 2

The Role of the Ghrelin Receptor in Appetite and Energy Metabolism

Stark, R., & Andrews, Z. B. (2014) · The Receptors · doi:10.1007/978-1-4939-0823-3_3 · Cited by 2

The immunometabolic function of VGLL3 and female-biased autoimmunity

Kennicott, K., & Liang, Y. (2024) · Immunometabolism · doi:10.1097/in9.0000000000000041 · Cited by 2

MLIP and Its Potential Influence on Key Oncogenic Pathways

Hamwi, M. N., Elsayed, E., Dabash, H., Abuawad, A., Aweer, N. A., Zeir, F. A., Pedersen, S., Al-Mansoori, L., & Burgon, P. G. (2024) · Cells · doi:10.3390/cells13131109 · Cited by 2

Aberrant activation of p53-TRIB3 axis contributes to diabetic myocardial insulin resistance and sulforaphane protection

Lu, G., Tang, Y., Chen, O., Guo, Y., Xiao, M., Wang, J., Liu, Q., Li, J., Gao, T., Zhang, X., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.07.025 · Cited by 3

Tumor Suppressor Genes

Brown, N. E., & Hinds, P. W. (2015) · Elsevier eBooks · doi:10.1016/b978-1-4557-4066-6.00003-2 · Cited by 2

Druggable sites/pockets of the p53-DNAJA1 protein–protein interaction: In silico modeling and in vitro/in vivo validation

Jacobsen, D. R., Bushara, O., Mishra, R. K., Sun, L., Liao, J., & Yang, G. (2022) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2022.07.005 · Cited by 2

Systematic Characterization of p53-Regulated Long Noncoding RNAs across Human Cancers Reveals Remarkable Heterogeneity among Different Tumor Types

Regunath, K., Fomin, V., Liu, Z., Wang, P., Hoque, M., Tian, B., Rabadán, R., & Prives, C. L. (2024) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-23-0295 · Cited by 2

HOPS/TMUB1 Enhances Apoptosis in TP53 Mutation-Independent Setting in Human Cancers

Di-Iacovo, N., Ferracchiato, S., Pieroni, S., Scopetti, D., Castelli, M., Piobbico, D., Pierucci, L., Gargaro, M., Chiasserini, D., Servillo, G., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094600 · Cited by 2

p53 Opens the Mitochondrial Permeability Transition Pore to Trigger Necrosis in Response to Oxidative Damage

Zirngibl, K., & Moll, U. M. (2014) · Springer eBooks · doi:10.1007/978-1-4614-8220-8_11 · Cited by 2

Targeting Cell Metabolism in Chronic Lymphocytic Leukaemia (CLL); Aviable Therapeutic Approach?

Clapham, C. E., Pettitt, A. R., & Slupsky, J. R. (2014) · Journal of Hematology and Oncology Research · doi:10.14302/issn.2372-6601.jhor-13-346 · Cited by 2

Chlamydia trachomatis disrupts host metabolism in primary cervical epithelial cells

Cheong, H. C., Rommel, M. I., Cheok, Y. Y., Chan, Y. T., Tang, T. F., Sulaiman, S., Looi, C. Y., Arulanandam, B. P., Chang, L., & Wong, W. F. (2025) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-025-04584-4 · Cited by 1

The influence of TC0668 on glycometabolism modulation in Chlamydia muridarum -infected host cells

Yu, N., Xuan, C., Yang, W., Zhou, Y., Hu, Y., & Zhou, Z. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.03051-24 · Cited by 1

Lactate, a Spearhead of Cancer Aggressiveness: Metabolic Reprogramming, Immune Suppression, and Metastatic Progression

Luqmani, Y. A. (2026) · Medical Principles and Practice · doi:10.1159/000552146 · Cited by 1

The p53–CerS6 interaction on the ER integrates p53 and sphingolipid signaling pathways in metabolic stress response

Childress, M. S., Jeffries, K. A., Horita, D. A., Krupenko, S. A., & Krupenko, N. I. (2026) · Journal of Lipid Research · doi:10.1016/j.jlr.2026.101097 · Cited by 1

p53 Arg72Pro polymorphism, adiposity status, and cancer risk: Two case‐cohorts within a Japanese prospective study

Nakano, S., Yamaji, T., Katagiri, R., Sawada, N., Inoue, M., Tsugane, S., & Iwasaki, M. (2022) · Cancer Science · doi:10.1111/cas.15572 · Cited by 2

ROS, Redox Regulation and Signaling in Cancer Cells

Bansal, M. P. (2023) · Springer eBooks · doi:10.1007/978-981-99-7342-2_1 · Cited by 1

Metabolic adaption of epithelial cells in asthma: a window to the initiation of carcinogenesis?

Dymond, T. (2024) · doi:10.37349/eaa.2024.00043 · Cited by 1

A model of STAT1-p53 coordination: Regulating p21 and PUMA to program cell fate under stress

Tshianyi, M. K. F. D., Omana, R. W., NDONDO, A. M., Didier, K. S., & Gonze, D. (2026) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2026.112491 · Cited by 1

Cancer as a metabolic disease and diabetes as a cancer risk?

Kaňková, K., & Hrstka, R. (2012) · PubMed · Cited by 1

Using Mouse Models and Making Sense of Them

Nguyen, D. H. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-25601-6_3 · Cited by 1

5-Fluorourasil (5-FU) ve C60 Nanopartikülünün Meme Kanseri (MCF-7) Hücre Hattı Üzerine Sitotoksik ve Apoptotik Etkilerinin Araştırılması

AYBEK, H., Ağca, C. A., & Çiftçi, M. (2020) · Türk doğa ve fen dergisi :/Türk doğa ve fen dergisi · doi:10.46810/tdfd.796339 · Cited by 1

Extracellular and Intracellular Magnesium Deficiency Found in Pregnant Women with Preeclampsia and Gestational Diabetes Is Associated with Overexpression of Notch Proteins, Cytokines, p53, NF-kB and Proto-Oncogenes: Potential Importance in Growth Retardation, Stillbirths, Fetal Mutations and Increased Cardiovascular Risks and Stroke with Advancing Age in Pregnant Women

Altura, B. M., Carella, A. V., Shah, N. C., Shah, N. C., Resnick, L. M., Handwerker, S. M., & Altura, B. T. (2021) · Hearts · doi:10.3390/hearts2010011 · Cited by 1

Phe19 modification of HDM2-p53 PPI inhibitors to alleviate CYP3A4 metabolism/mechanism-based inhibition liability

Tian, Y., Lahue, B. R., Ma, Y., Nair, L. G., Pan, W., Doll, R. J., Guzi, T. J., Ma, Y., Wang, Y., & Bogen, S. L. (2022) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2022.128625 · Cited by 1

Reactive oxygen species in the progression and treatment of malignant mesothelioma

Cote, A., Messier, T., & Cunniff, B. (2022) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2022.41 · Cited by 1

The dynamic relationship between inorganic polyphosphate and adenosine triphosphate in human non‐small cell lung cancer H1299 cells

Tsutsumi, K., Tippayamontri, T., Hayashi, M., Matsuda, N., & Goto, Y. (2023) · FEBS Open Bio · doi:10.1002/2211-5463.13753 · Cited by 1

Therapeutic Effects of Cephalotaxus harringtonia Leaf Extract on Hepatocellular Carcinoma via Regulation of the Intrinsic Apoptosis Pathway and Cell Cycle

Park, D.-H., Ramos, S., Sim, H. B., Lee, J.-B., Jang, H.-Y., Jeong, B.-G., Park, K.-W., Kang, K.-Y., & Kim, J.-J. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47120994 · Cited by 1

p53: Point Mutations, SNPs and Cancer

Fang, M., Simeonova, I., & Toledo, F. (2012) · InTech eBooks · doi:10.5772/33715 · Cited by 1

Cancer Cells as Dynamic System – Molecular and Phenotypic Changes During Tumor Formation, Progression and Dissemination

Sommerová, L., Ondroušková, E., & Hrstka, R. (2016) · Klinicka onkologie · doi:10.14735/amko20164s6 · Cited by 1

Cadmium Toxicity Showing Organ Specific Signature of Responsiveness

Agnihotri, S. K., & Ghosh, I. (2017) · Environmental science and engineering · doi:10.1007/978-3-319-46248-6_4 · Cited by 1

Alterations in Metabolite-Driven Gene Regulation in Cancer Metabolism

Jha, S. K., Yadav, R., Swati, K., Jha, N. K., Sharma, A., Khan, F., Kumar, N., Nand, P., Kaur, P., Gover, T., et al. (2020) · Springer eBooks · doi:10.1007/978-981-15-1991-8_10 · Cited by 1

Co nás učí nádory. Paralely v chování buněk a lidí

Šmardová, J. (2021) · Masarykova univerzita eBooks · doi:10.5817/cz.muni.m210-9700-2021 · Cited by 1

Cancer Biology and Implications for the Perioperative Period

Perry, N. J. S., Jhanji, S., & Poulogiannis, G. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-69584-8.00003-7 · Cited by 1

Oocyte Metabolism and Its Relationship to Developmental Competence

Krisher, R. L., & Herrick, J. R. (2013) · Wiley eBooks · doi:10.1002/9781118538074.ch9 · Cited by 1

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Gourgiotis, A., Isnard, H., Nonell, A., Aubert, M., Stadelmann, G., Dupont, E., Almahamid, I., Tiang, G., Rao, L., Lukens, W. W., et al. (2013) · Cited by 1

Potencial antiproliferativo do monofosfoester 2-aminoetil dihidrogeno fosfato associado ao peptídeo penetrante de tumor BR2 em células tumorais de mama triplo-negativo

Cabral, L. G. D. S. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.5.2021.tde-17082021-101606 · Cited by 1

p53-induced RNA-binding protein ZMAT3 inhibits transcription of a hexokinase to suppress mitochondrial respiration in human cancer cellsPreprint

Kumar, R., Couly, S., Muys, B. R., Li, X. L., Grammatikakis, I., Singh, R., Guest, M., Wen, X., Tang, W., Ambs, S., et al. (2025) · eLife · doi:10.7554/elife.107538 · Cited by 1

Exposome du cancer : reprogrammation métabolique du cancer du poumon par les nitrosamines spécifiques de la fumée de tabac

Sarlak, S. (2021) · theses.fr (ABES) · doi:10.70675/2e2c5420z3a1fz49c3zb548z8e72b24a52b2 · Cited by 1

The Role of Protein Kinase CK2 in the p53 Response

Meek, D. W. (2013) · Wiley eBooks · doi:10.1002/9781118482490.ch6

Cell lineage choice during differentiation of trophoblast stem cells (tsc) is dependent on oxygen levels, and mediated by stress enzyme pathways and mitochondrial function

Zhou, S. (2011) · Human Biology

Global Molecular and Cellular Measurement Technologies

Lange, B. M. H., Schweiger, M. R., & Lehrach, H. (2011) · Springer eBooks · doi:10.1007/978-94-007-1567-7_3

Wig-1: A p53 target that regulates the mRNA of p53 and Myc - and more?

Vilborg, A. (2010) · Figshare

Cell Death and Neurodegeneration

Pivtoraiko, V. N., & Roth, K. A. (2011) · Wiley eBooks · doi:10.1002/9781444341256.ch2

Molecular regulation of forebrain development and neural stem/progenitor cells

Hakanen, J. (2014) · Työväentutkimus Vuosikirja

NEW TARGET GENES FOR TUMOR SUPPRESSORS p53 AND p73 IN REGENERATING LIVER

Kurinna, S. M. (2010) · Digital Commons-TMC (Texas Medical Center)

Oxidative Stress‐Mediated Signaling Pathways by Environmental Stressors

Sone, H., & Akanuma, H. (2011) · Wiley eBooks · doi:10.1002/9781118148143.ch13

Cellular Basis for Learning Impairment in Fragile X Syndrome

Larson, J. R. (2013) · Defense Technical Information Center (DTIC) · doi:10.21236/ada586251

Effect of aberrant ribosome biogenesis on wild-type and mutant p53 in cancer cells

Ferro, M. D. (2014) · OpenstarTs (Univeristy of Trieste https://www.units.it/)

Caracterização imunogenética de variantes dos genes CCR2, CCR5 e HLA-G como potenciais alvos para diagnóstico, prognóstico e tratamento do câncer de mama feminino esporádico e familial

Giongo, C. D. O. (2012) · Americanae (AECID Library)

Associations of sex, anthropometric and reproductive factors with clinicopathological and molecular characteristics of colorectal cancer

Brändstedt, J. (2014) · Lund University Publications (Lund University)

Modulation of p53's transcriptional function by small molecules

Nikulenkov, F. (2011) · Figshare

Hdm2 Small-Molecule Inhibitors For Therapeutic Intervention In B-Cell Lymphoma

Sosin, A. M. (2012) · Human Biology

BIOENERGETICS, THE FOUNDATION OF THE FUTURE OF CANCER THERAPEUTICS A QUANTUM LEAP IN MAKING

Afrasiabi (2012) · OnLine Journal of Biological Sciences · doi:10.3844/ojbsci.2012.108.112

Initial Characterization of a Low-Molecular-Weight Factor Enhancing the Checkpoint Response

Fan, X., Cheong, N., & Iliakis, G. E. (2010) · Radiation Research · doi:10.1667/rr2165.1

The Effect of MCT1 and MCT4 silencing on Prostate Cancer Survival and Aggressiveness

Sousa, S. P. S. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/6kkm-bc75

Energy balance and cancer risk : metabolic and molecular studies

Wheatley, K. E. (2010) · Texas ScholarWorks (Texas Digital Library)

Small molecule inhibitors of Mdm2 E3 ubiquitin ligase activity

Dickens, M. P. (2011) · UPT. Syiah Kuala University Library (Syiah Kuala University)

Otto Warburg's contributions to current concepts of cancer metabolism

Butenandt, A. (2011)

The possible link between high glucose-induced PKCβ expression and the appearance of GLP-1 resistance in endothelial cells

Nigris, V. D. (2015) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Canagliflozin Potently Activates AMPK and Inhibits the Growth and Survival of Cancer Cells

Villani, L. A. (2015) · MacSphere (McMaster University) · doi:10.71548/8610

Cell Death Induction by Targeting Tumor Metabolism

von Schwarzenberg, K. (2015) · InTech eBooks · doi:10.5772/61480

Mechanisms of Gastrointestinal Carcinogenesis

Scott, F. I., & Lynch, J. P. (2012) · Molecular pathology library · doi:10.1007/978-1-4614-6015-2_1

KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE

Cyr, D. P. (2013)

Regulation of neuronal death by the autophagy lysosomal pathway: Implications for Parkinson disease

Pivtoraiko, V. N. (2011) · ProQuest Demo Repository

IN VIVO SIGNIFICANCE OF THE MDM4 AND P73 INTERACTION DURING DEVELOPMENT AND TUMORIGENESIS

Tashakori, M. (2015) · Digital Commons-TMC (Texas Medical Center)

Most cancer cells use aerobic glycolysis to fuel their growth. The enzyme lactate dehydrogenase-A (LDH-A) is key to cancer's glycolytic phenotype, catalysing the regeneration of nicotinamide adenine dinucleotide (NAD þ ) from reduced nicotinamide

Allison, S., Knight, J. R. P., Granchi, C., Rani, R., Minutolo, F., Milner, J., & Phillips, R. M. (2014)

Antagonism between gene therapy and epigenetic therapy on human laryngeal carcinoma tumor-bearing mice

Lian, M., Wang, Q., Fang, J., Wang, H., & Fan, E. (2013) · Chinese Medical Journal · doi:10.3760/cma.j.issn.0366-6999.20120063

Znaczenie metabolizmu glukozy w diagnostyce oraz terapii nowotworów układów krwiotwórczego i chłonnego

Malenda, A., & Nowis, D. (2013) · Via Medica Journals

CROSS-TALK BETWEEN THE UBIQUITIN-PROTEASOME SYSTEM AND MACROAUTOPHAGY

Pankiv, S., & Johansen, T. (2012) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814350457_0003

Biomarkers of Oxidative Stress as Predictors of Breast Cancer Risk in Women and Adolescent Girls

Brennan, L. A. (2016) · ProQuest Demo Repository · doi:10.7916/d8gt5ngp

The regulation of DNA damage signalling and repair by MOB2

Gündoğdu, R. (2016) · UCL Discovery (University College London)

Control of Cardiomyocyte Proliferation by p53/MDM2-Regulated microRNAs

Stanley-Hasnain, S. (2016) · TSpace (University of Toronto)

Investigation into the Role of Antioxidants in Tumorigenesis

Harris, I. S. (2014) · Library and Archives Canada (Government of Canada)

An investigation of mutant p53 function.

Noll, J. E. (2011) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

Comparative transcriptional profiling and differential expression analysis of pectoralis major muscle in modern and legacy Gallus broiler lines

Davis, R. V. N. (2017) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/wy2h-at19

Towards the Investigation of the Effects of Nitration on the Activity of the Human p53 Tumour Suppressor Protein. Nitration of the p53 Tumour Suppressor Protein

Husaini, R. (2014) · Bradford Scholars (University of Bradford)

A New Insight into the Development of Novel Anti-Cancer Drugs that Improve the Expression of Mitochondrial Function-Associated Genes

Uchiumi, F., Arakawa, J., Takihara, Y., Akui, M., Hamada, H., & Tanuma, S. (2018) · InTech eBooks · doi:10.5772/intechopen.71095

Comprehensive Relevance of AMPK in Adaptive Responses of Physical Exercise, Skeletal Muscle and Neuromuscular Disorders

Lee, J.-H. (2018) · Journal of the Korean Society of Physical Medicine · doi:10.13066/kspm.2018.13.3.141

Studies on geranylgeranoic acid-induced cell death: with special attention to pyroptosis in human hepatoma cells

Yabuta, S. (2018) · Institutional Repositories DataBase (IRDB)

The role of PATZ1 transcription factor in the DNA damage response

Deniz, E. (2014) · Sabanci University

In Vivo Discoveries in MDM2-Mediated p53 Regulation

Tackmann, N. R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/z7ta-7m83

Roles of hepatitis B X-interacting protein in tumor development

Wang, X., Jin, T., Ye, L., Zhang, W. Q., & Fu, X. (2019) · Scientia Sinica Vitae · doi:10.1360/ssv-2019-0159

Glucose transporter 1 and prognosis in cancer

Sawayama, H., & Baba, H. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-849886-6.00007-0

Novel preclinical models, therapies and biomarkers for testicular cancer

Plaza, F. X. R. (2020) · doi:10.33612/diss.119056452

The role of c-jun n-terminal kinase (JNK) and tumour protein (p53) in HIV associated pre-eclampsia.

Pillay, Y. (2017) · ResearchSpace (University of KwaZulu-Natal)

Cell death mechanisms—Apoptosis pathways and their implications in toxicology

Madkour, L. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-822481-6.00009-8

Tumor suppressor p53 and its mutants in cancer metabolism

Liu, J., Zhang, C., Hu, W., & Feng, Z. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.12.025 · Cited by 276

The latest research progress on P53 and tumor metabolism

ZHAI Haihui, L. Y. (2023) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.19401/j.cnki.1007-3639.2023.11.009

Taking up the reins of power: metabolic functions of p53

Humpton, T. J., & Vousden, K. H. (2019) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjz065 · Cited by 29

Metabolic regulation by p53: Implications for cancer therapy

Koo, K. Y., Moon, K., He, S., & Lee, M.-S. (2025) · Molecules and Cells · doi:10.1016/j.mocell.2025.100198 · Cited by 45

Emerging Roles of the Tumor Suppressor p53 in Metabolism

Yu, L., Wu, M. Y., Zhu, G., & Xu, Y. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.762742 · Cited by 49